It is generally accepted that CD8+ T cell responses play an important role in control of immunodeficiency virus replication. The association of HLA-B27 and -B57 with control of viremia supports this conclusion. However, specific correlates of viral control in individuals expressing these alleles have been difficult to define. We recently reported that transient in vivo CD8+ cell depletion in simian immunodeficiency virus (SIV)-infected elite controller (EC) macaques resulted in a brief period of viral recrudescence. SIV replication was rapidly controlled with the reappearance of CD8+ cells, implicating that these cells actively suppress viral replication in ECs.
Methods and Findings
Here we show that three ECs in that study made at least seven robust CD8+ T cell responses directed against novel epitopes in Vif, Rev, and Nef restricted by the MHC class I molecule Mamu-B*08. Two of these Mamu-B*08-positive animals subsequently lost control of SIV replication. Their breakthrough virus harbored substitutions in multiple Mamu-B*08-restricted epitopes. Indeed, we found evidence for selection pressure mediated by Mamu-B*08-restricted CD8+ T cells in all of the newly identified epitopes in a cohort of chronically infected macaques.
Together, our data suggest that Mamu-B*08-restricted CD8+ T cell responses effectively control replication of pathogenic SIVmac239. All seven regions encoding Mamu-B*08-restricted CD8+ T cell epitopes also exhibit amino acid replacements typically seen only in the presence of Mamu-B*08, suggesting that the variation we observe is indeed selected by CD8+ T cell responses. SIVmac239 infection of Indian rhesus macaques expressing Mamu-B*08 may therefore provide an animal model for understanding CD8+ T cell-mediated control of HIV replication in humans.
Citation: Loffredo JT, Friedrich TC, León EJ, Stephany JJ, Rodrigues DS, Spencer SP, et al. (2007) CD8+ T Cells from SIV Elite Controller Macaques Recognize Mamu-B*08-Bound Epitopes and Select for Widespread Viral Variation. PLoS ONE 2(11): e1152. doi:10.1371/journal.pone.0001152
Academic Editor: Douglas Nixon, University of California at San Francisco, United States of America
Received: October 3, 2007; Accepted: October 12, 2007; Published: November 14, 2007
Copyright: © 2007 Loffredo et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This research was supported by National Institutes of Health (NIH) contract HHSN266200400088C, NIH grants R01 AI049120, R01 AI052056, R24 RR015371, and R24 RR016038 to D.I.W. as well as R21 AI068586 to T.C.F. Additionally, this publication was made possible in part by grant number P51 RR000167 from the National Center for Research Resources (NCRR), a component of the NIH, awarded to the WNPRC. This project has also been funded in part by a grant from the Japan Health Sciences Foundation to D.I.W., NIH grant GM43940 to A.L.H., and support to H.P. through the Kent State University Research Council and Ohio Board of Regents Research Challenge Grant. D.A.P. is a Medical Research Council (UK) Senior Clinical Fellow. This work was conducted in part at a facility constructed with support from Research Facilities Improvement grant numbers RR15459-01 and RR020141-01 (WNPRC). This publication's contents are solely the responsibility of the authors and do not necessarily represent the official views of NCRR or NIH.
Competing interests: The authors have declared that no competing interests exist.
Several lines of evidence suggest that CD8+ T cells play a key role in immune control of immunodeficiency virus replication. The reduction in acute viremia is associated with the appearance of CD8+ T cell responses in both HIV-infected humans ,  and SIV-infected macaques , , though recent experiments suggest that this reduction could also be due to the acute depletion of memory CD4+ T cells that are the preferred targets for infection , . Expression of particular HLA/MHC class I alleles is associated with reduced plasma viremia and/or slower disease progression in humans – and macaques –. CD8+ T cell responses also exert selective pressure on replicating viruses, resulting in the emergence of variants that escape immune detection in both HIV and SIV infection –. Most strikingly, transient depletion of circulating CD8+ lymphocytes in SIV-infected macaques results in dramatic increases in plasma viremia –. These findings suggest that inducing CD8+ T cell responses will be an important component of AIDS vaccine strategies. However, because most HIV- and SIV-infected individuals mount CD8+ T cell responses, and the majority of these individuals progress to AIDS, it is clear that the presence of strong responses alone is not sufficient to control viral replication or delay disease progression. Therefore, it is important to define attributes that might distinguish effective CD8+ T cell responses from ineffective ones.
In the effort to define such correlates of control for CD8+ T cells, there has been considerable interest in “elite controllers” (ECs), rare individuals who spontaneously control HIV viremia to levels below the detection threshold of current assays (<50 vRNA copy Eq/ml plasma) . Effective control of HIV replication in some such individuals could be mediated by determinants other than cellular immunity, such as infection with attenuated viruses –, polymorphisms in host genes outside the MHC –, or autoimmune antibodies directed against the CCR5 coreceptor , . However, there is strong evidence suggesting that particular CD8+ T cell responses play a major role in effective viremia control in at least some ECs. Vigorous CD8+ T cell responses have been observed in individuals with non-progressive infection , . Investigation of the phenotypes of HIV-specific CD8+ T cells has suggested that controllers retain effector functions that are lost in progressors –. The MHC class I alleles HLA-B27 and HLA-B57/B*5801 are over-represented in cohorts of ECs, suggesting that the cellular immune responses they restrict contribute to immune containment of viral replication –. In support of this suggestion, viral escape from the immunodominant response to the HLA-B27-restricted epitope Gag263–272KK10 has been associated with loss of control of viral replication , –. The role of viral evolution and particular epitope-specific responses in control associated with HLA-B57, however, remains less clear .
Studies of elite HIV control in humans are limited by drawbacks inherent to research in populations infected with diverse virus strains. An animal model of effective viremia control would complement these studies by offering an example of successful immune containment of pathogenic AIDS virus replication while allowing direct control over key variables such as virus strain, host genotype, and timing and route of infection. To this end, several studies have noted relationships between MHC class I genotypes and effective control of viremia in cohorts of SIV-infected rhesus macaques that mirror those seen in human EC cohorts. Expression of the common MHC class I allele Mamu-A*01 has been observed to lower set-point viremia in vaccinated and non-vaccinated macaques in several studies –, . More strikingly, we have recently reported an association between a different high-frequency MHC class I allele, Mamu-B*17, and an even greater reduction of chronic phase viremia . Mamu-B*17, but not Mamu-A*01, was also over-represented in a cohort of EC macaques that maintained chronic phase SIV viremia <1,000 vRNA copy Eq/ml , .
To test the hypothesis that CD8+ T cell responses are involved in the ongoing control of viremia in EC macaques, we recently treated six ECs (four Mamu-B*17-positive, two Mamu-B*17-negative) with the monoclonal antibody cM-T807, which transiently depletes circulating CD8+ lymphocytes . This treatment resulted in a brief viral recrudescence in all six ECs, after which viremia declined back to near pre-depletion levels. Analysis of the returning wave of CD8+ T cells showed different degrees of expansion in epitope-specific populations in each animal. We noted that the two Mamu-B*17-negative macaques shared expanding CD8+ T cell populations that recognized previously unmapped epitopes in the SIV proteins Vif and Nef. Here we report minimal optimal sequences for these novel epitopes and show that they are presented by the MHC class I molecule Mamu-B*08.
We recently discovered that Mamu-B*08 is strongly associated with control of SIVmac239 replication . We have extended this finding, showing that Mamu-B*08 presents at least seven CD8+ T cell epitopes derived from SIVmac239. Furthermore, we show that the sequences of viruses replicating during chronic infection have substitutions in several Mamu-B*08-restricted epitopes, indicating that CD8+ T cells restricted by this molecule exert selective pressure on the virus at multiple sites. We also report the construction of Mamu-B*08 tetramers loaded with each of the newly discovered epitope peptides, enabling us to determine the chronic-phase immunodominance hierarchy of these responses.
Animals and viruses
Indian rhesus macaques (Macaca mulatta) were initially identified as Mamu-B*08-positive by analysis of MHC class I cDNA libraries. PCR with sequence-specific primers (PCR-SSP) was used as previously described  for confirmation and to identify additional Mamu-B*08-positive macaques. Animals were screened for the presence of nine additional MHC class I alleles (Mamu-A*01, -A*02, -A*08, -A*11, -B*01, -B*03, -B*04, -B*17, and -B*29) using PCR-SSP as previously described , .
Animals were infected with the pathogenic molecular clone SIVmac239  (GenBank accession M33262), with the exception of macaque r99006, which was infected with an SIVmac239 recombinant bearing escape mutations in three CD8+ T cell epitopes , . Animals' plasma virus concentrations were monitored by quantitative PCR as previously described , .
EC macaques r00078, r01064, and r98016 were transiently depleted of CD8+ lymphocytes as part of a prior study . These three ECs and animal r99006 were subsequently rechallenged intravenously with 100 TCID50 SIVmac239 with no effect on viremia or the frequency of SIV-specific CD8+ T cells (Friedrich et al., unpublished data).
SIV-infected animals were maintained at the National Primate Research Center (University of Wisconsin-Madison, Madison, WI) and cared for according to the regulations and guidelines of the University of Wisconsin Institutional Animal Care and Use Committee.
Construction of MHC class I cDNA libraries
Total RNA from animals r00078, r01064, and r98016 was isolated from ∼3×107 cells from B-lymphoblastoid cell lines (BLCL) using the RNeasy Protect Mini Kit (QIAGEN, Valencia, CA). For each animal, ∼3 µg mRNA was isolated from 150 µg total RNA using the Oligotex Midi Kit (QIAGEN). One microgram of mRNA from each animal served as the template for first strand cDNA synthesis, using the SuperScript plasmid system for cDNA synthesis and cloning (Invitrogen, Carlsbad, CA) by following the manufacturer's instructions. Size-fractionated cDNA containing SalI and NotI restriction endonuclease cohesive ends was ligated into the multiple cloning site of pCMV.SPORT6 and used to transform DH5α chemically competent E. coli (Invitrogen). Recombinant plasmids containing cDNA were isolated from ∼5×105 ampicillin resistant colonies and purified using the HiSpeed Plasmid Midi kit (QIAGEN). Five micrograms of plasmid DNA from each macaque's library served as the target DNA for hybridization to a biotinylated oligonucleotide, 5′-CGGAGATCAYRCTGACVTGGC-3′. The sequence of the capture oligonucleotide was derived from a highly conserved region of the MHC class I alpha-3 domain. The GeneTrapper cDNA positive selection system (Invitrogen) was then used to enrich the cDNA library for MHC class I alleles.
More than 150 MHC class I clones were captured and sequenced from each library. Sequencing was performed on an ABI 3730 DNA Analyzer (Applied Biosystems, Foster City, CA). Full-length sequences of MHC class I cDNAs were obtained by using four forward and four reverse primers. The forward primers were: SP6 (5′-GGCCTATTTAGGTGACACTATAG-3′), C/1+ (5′-GCAGATACCTGGAGAACGGG-3′), IV (5′-GGAACCTTCCAGAAGTGGG-3′), and 3′UTR (5′-CAGGGCTCTGATGTGTCTCTCACG-3′). The reverse primers were: T7 (5′-TAATACGACTCACTATAGGG-3′), E2 (5′-CYCCACCTCCTCACATKATGC-3′), F1 (5′-CCAGGTCAGTGTGATCTCCG-3′), and G1 (5′-ATGTAATCCTTGCCGTCGTA-3′). Sequences were analyzed using CodonCode Aligner version 1.6.3 (CodonCode, Deadham, MA). MHC class I alleles were considered part of the cDNA library after at least two copies were verified by sequencing. Novel MHC I sequences were given GenBank accession numbers: Mamu-A6*0103 (EF602318), referred to as Mamu-A*15 in Table 1, Mamu-B*31 (EF602319), and Mamu-B*5102 (EF362450).
Generation and maintenance of SIV-specific CD8+ T cell lines
Peptide-specific CD8+ T cell lines were generated using previously described methods , . Briefly, freshly isolated PBMC or CD8+ cell-enriched PBMC were used to start CD8+ T cell lines. Autologous B-lymphoblastoid cell lines (BLCL) were used as antigen presenting cells (APCs). BLCL were pulsed with 1 µM relevant SIV-specific peptide for 1 to 2 hours at 37°C, washed twice, and irradiated (9,000 rads). BLCL were then mixed with either whole or CD8+ cell-enriched PBMC at a ratio of 1∶1 in RPMI 1640 (Cambrex, Walkersville, MD) supplemented with L-glutamine (Mediatech, Herndon, VA), antibiotic-antimycotic solution (Mediatech), and 15% fetal bovine serum (FBS; HyClone, Logan, UT) (R15) with 10 ng/ml of recombinant human interleukin-7 (Sigma-Aldrich, St. Louis, MO) and incubated for 48 hours. Cells were cultured with R15 containing 100 Units of interleukin-2/ml (NIH AIDS Research and Reference Reagent Program, Germantown, MD) (R15-100) every 3 to 5 days thereafter. The CD8+ T cell lines were restimulated using peptide-pulsed, irradiated BLCL every 7 to 14 days. CD8+ T cell lines were tested for epitope specificity after >14 days in culture by either intracellular cytokine staining (ICS) or MHC class I tetramer assays as previously described -. MHC class I tetramers were constructed with minor modifications as previously described , .
MHC class I transfectants
Transient expression of cloned MHC class I cDNA was achieved by electroporation of plasmid DNA into the MHC class I deficient human B-cell line 721.221 . Briefly, 5 µg of plasmid DNA was added to 5×106 721.221 cells in 100 µl of Nucleofector™ Solution C and electroporated using program G-16 on a Nucleofector I device (Amaxa, Köln, Germany). Maximum cell surface expression occurred four days post-electroporation. The stable Mamu-B*08 transfectant was created as previously described , , except for the use of the Nucleofector I device (Amaxa) according to manufacturer's protocols.
MHC class I surface expression on stable and transient MHC class I transfectants was measured by W6/32 antibody surface staining. Staining was also performed on the 721.221 cells as a negative control and immortalized macaque B-cell lines (positive control). Approximately 0.5–1×105 lymphocyte-gated events were acquired on a FACSCalibur (BD Biosciences, San Jose, CA) and analyzed using FlowJo version 8.4.5 (TreeStar, Ashland, OR).
Intracellular cytokine staining (ICS) assay
TNF-α and IFN-γ intracellular cytokine staining (ICS) assays were performed on both freshly isolated PBMC and SIV-specific CD8+ T cell lines as previously described , , . Briefly, each PBMC ICS test contained ∼5×105 cells, while each CD8+ T cell line ICS test contained 2×105 CD8+ T cells along with 1×105 autologous BLCL. Individual peptides were used at a concentration of 5 µM or in serial ten-fold dilutions ranging from 5 µM to 5 pM. SIV peptide pools each contained ten 15-mer peptides overlapping by eleven amino acids. Approximately 0.5–1×105 lymphocyte-gated events were acquired on a FACSCalibur (BD Biosciences) and analyzed using FlowJo 8.4.5 (TreeStar). All values were normalized by subtracting the background (cytokine-positive events in negative control samples of PBMC or CD8+ T cell lines in media without stimulation).
IFN-γ Enzyme-Linked Immunospot (ELISPOT) assay
ELISPOT assays were performed as previously described . Briefly, freshly isolated PBMC were used directly in precoated ELISpotPLUS kits (MABTECH Inc, Mariemont, OH) for the detection of monkey IFN-γ according to manufacturer's protocols. 1×105 PBMC were used per well and incubated 14–18 hours at 37°C in 5% CO2. Peptides were used at 10 µM or in serial ten-fold dilutions ranging from 10 µM to 10 pM. SIV peptide pools each contained ten 15-mer peptides overlapping by eleven amino acids. All tests were performed in either duplicate or triplicate.
Wells were imaged with an AID ELISPOT reader (AID, Strassberg, Germany), counted by AID EliSpot Reader version 3.2.3, and analyzed as previously described , . Background (mean number of spot-forming cells [SFCs] in wells without peptide stimulation) was subtracted from each well on the plate. A response was considered positive if the mean number of SFCs from triplicate or duplicate sample wells exceeded background plus two standard deviations (SD). Assay results are shown as SFCs per 1×106 PBMC. Responses <50 SFCs per 1×106 PBMC were not considered positive.
Sequencing of plasma viral RNA
Viral sequencing was performed essentially as previously described , . Briefly, viral RNA was extracted from plasma using the QIAGEN MinElute kit. We used the QIAGEN One Step RT-PCR kit to amplify overlapping regions ∼300–800 nucleotides in length that spanned the SIVmac239 open reading frames (ORFs) vif, rev, or nef. The RT-PCR conditions for all amplicons were as follows: 50°C for 30 min; 95°C for 15 min; 45 cycles of 94°C for 30 s, 53°C for 1 min and 72°C for 150 s; and 68°C for 20 min. Cycling ramp rates were 2°C per second. The amplified cDNA was purified using the QIAGEN PCR purification kit. For some extremely low copy number samples (<100 vRNA copy Eq/ml) PCR products were directly cloned into the pCR®4-TOPO® vector using the TOPO-TA Cloning Kit (Invitrogen). Plasmids containing cloned sequences were purified using the QIAprep Spin Miniprep Kit (QIAGEN). Both strands of each amplicon were sequenced on a 3730 DNA Analyzer (Applied Biosystems). Sequences were assembled using Aligner version 1.6.3 (CodonCode). DNA sequences were conceptually translated and aligned to wild type SIVmac239 in MacVector 9.0 trial version (Accelrys, Burlington, MA).
Statistical analysis of viral variation
The number of synonymous substitutions per synonymous site (dS) and the number of nonsynonymous substitutions per nonsynonymous site (dN) between the viral sequence obtained from each animal's circulating virus and the inoculum sequence (SIVmac239) were estimated using the method of Nei and Gojobori , and the results were analyzed as previously described , . In the case of ambiguous nucleotides, we assumed equal occurrences of the possible nucleotides in the viral population in any given monkey. Note that, since the virus evolved independently in each monkey, comparisons of viral sequences with the inoculum are both statistically and phylogenetically independent .
Mamu-B*17-negative ECs share robust responses to novel epitopes derived from Vif and Nef
While the majority of SIV ECs express Mamu-B*17 , several do not. In an attempt to define the immune correlates of control, we depleted CD8+ cells in vivo from four Mamu-B*17-positive and two Mamu-B*17-negative ECs . In this transient CD8+ cell depletion experiment, particular virus-specific CD8+ T cells repopulating the periphery expanded above baseline frequencies. The set of epitopes recognized by expanding populations was different in each animal, but in each case previously subdominant populations showed a much greater relative expansion than dominant ones. We hypothesized that these expanding CD8+ T cell populations played an important role in the re-assertion of control over SIV replication.
Expanding CD8+ T cell populations in the four Mamu-B*17-positive ECs after depletion targeted epitopes in Vif and Nef . Interestingly, expanding populations in the two Mamu-B*17-negative ECs, r00078 and r01064, also responded to peptides derived from these proteins (Fig. 1A). Indeed, both Mamu-B*17-negative ECs had large populations of CD8+ lymphocytes that recognized the same pool of ten Vif 15-mer peptides, Vif E (SIVmac239 Vif residues 161-214). To determine whether the animals might be recognizing the same epitope, we mapped the minimal optimal epitope recognized by both animals. First, we deconvoluted the 15-mer peptide pool, testing the ability of each individual 15-mer to stimulate IFN-γ secretion by the animals' PBMC in ICS assays. These experiments showed that the response to the pool was recapitulated by stimulation with either of two individual 15-mers (Fig. 1B). Since the responses to each 15-mer were very similar in magnitude for both animals, we reasoned that the minimal optimal epitope was contained within the region of overlap for the two peptides. IFN-γ ELISPOT assays using dilutions of candidate minimal optimal peptides showed the epitope recognized by each animal to be an 8-mer, RRDNRRGL, Vif172–179RL8 (Fig. 1C).
MHC class I alleles detected by PCR-SSP are listed for each animal. A) Unknown CD8+ responses from ex vivo ICS assays using SIV peptide pools performed one month prior to (white bars) and four weeks after (black bars) CD8+ cell depletion. Responses to 15-mer pools that did not contain previously identified minimal optimal epitope sequences , ,  are summed for each protein. Of particular interest was an unknown SIV-specific CD8+ response directed against Vif, which expanded in two Mamu-B*17-negative ECs r00078 and r01064. B) Ex vivo ICS deconvolution of peptide pool Vif E (positions 161–214) using r00078 PBMC demonstrated that the novel CD8+ epitope was located within two overlapping 15-mers in Vif (positions 165–183). C) Ex vivo IFN-γ ELISPOT using peptide dilutions in r00078 fine-mapped the novel CD8+ epitope to an 8-mer at positions 172–179 in Vif (RRDNRRGL). Mean values from triplicate wells were calculated for each peptide test.
We also noted a strong response to an unidentified epitope in a third EC, r98016. More than 3% of this animal's returning CD8+ lymphocytes responded to a pool of Nef-derived 15-mers, Nef D (SIVmac239 Nef residues 125–179) (Fig. 2A). This peptide pool contains previously described dominant epitopes bound by Mamu-A*02 (Nef159–167YY9) ,  and Mamu-B*17 (Nef165–173IW9) , , . Surprisingly, although r98016 expressed both Mamu-A*02 and B*17, only ∼0.1% of its CD8+ lymphocytes recognized the Nef165–173IW9 peptide, while responses to Nef159–167YY9 were undetectable (Fig. 2A). The Mamu-A*02-negative, Mamu-B*17-negative EC r00078 also made a strong response to the same Nef pool after CD8+ cell depletion (0.26% CD8+ IFN-γ+, Fig. 1A and data not shown). We therefore hypothesized that these animals made a CD8+ T cell response to a novel epitope in Nef, which was not presented by either Mamu-A*02 or -B*17. To test this hypothesis, we first deconvoluted the response to Nef pool D in r98016 using ICS for IFN-γ and TNF-α. The strongest response to an individual peptide was stimulated by a single 15-mer, Nef137–151 (Fig. 2B). No 8-mer or 9-mer Nef peptide in this region elicited a similarly strong response (data not shown). To define the minimal optimal epitope we then tested the ability of serial ten-fold dilutions of larger candidate peptides (ten to twelve amino acids in length) to stimulate IFN-γ and TNF-α secretion in ICS assays using Nef-specific CD8+ T cell lines from animal r98016 (Fig. 2C). Although the 10-mer, 11-mer, and 12-mer all showed similar functional avidity, we defined the 10-mer as the minimal optimal, since it was the shortest peptide to stimulate the maximal response. The sequence of this peptide was RRHRILDIYL, Nef137–146RL10. IFN-γ ELISPOT assays using PBMC gave similar results, further suggesting that Nef137–146RL10 was the minimal optimal epitope recognized by r98016 (data not shown). PBMC from animals r00078 and r01064 also recognized overlapping 15-mer peptides containing this 10-mer sequence (see below), suggesting that all three ECs responded to this same epitope. MHC class I tetramer refolding subsequently confirmed that Nef137–146RL10 is the minimal optimal epitope bound by Mamu-B*08 (data not shown).
MHC class I alleles detected by PCR-SSP are listed for r98016. A) Unknown CD8+ responses from ex vivo ICS assays using SIV peptide pools performed one month prior to (white bars) and four weeks after (black bars) CD8+ cell depletion. Responses to 15-mer pools that did not contain previously identified minimal optimal epitope sequences [i.e., Nef159–167YY9 and Nef165–173IW9] , ,  are summed for each protein. Of particular interest was an unknown SIV-specific CD8+ response directed against Nef, which expanded in Mamu-B*17-positive EC r98016. B) Ex vivo ICS deconvolution of peptide pool Nef D (positions 125–179) using r98016 PBMC revealed that the novel CD8+ epitope was located within two overlapping 15-mers in Nef (positions 133–151). C) ICS results using peptide dilutions with a Nef-specific CD8+ T cell line from r98016 fine-mapped the novel CD8+ epitope to a 10-mer at positions 137–146 in Nef (RRHRILDIYL).
CD8+ T cells from SIV EC macaques recognized novel Mamu-B*08-restricted epitopes
It appeared that all three ECs recognized the same novel Nef137–146RL10 epitope, RRHRILDIYL, while at least two animals, r00078 and r01064, recognized the novel Vif172–179RL8 epitope RRDNRRGL. Both these peptides had a diarginine motif at their N-termini and a leucine residue at their C-termini. Furthermore, BLCL derived from all three animals could present peptides to Vif172–179RL8-specific CD8+ T cell lines from animals r00078 and r01064 and also to Nef137–146RL10-specific CD8+ T cell lines generated from r98016 (data not shown). We therefore hypothesized that the novel epitopes were bound by the same, as yet unidentified, MHC class I molecule.
All ECs in the CD8+ cell depletion study had been screened for the presence of nine MHC class I alleles by sequence-specific PCR (PCR-SSP). Animals r00078, r01064, and r98016 did not share an allele detected in this screen (Figs. 1 and 2). PCR-SSP is useful as a high-throughput screen for the presence or absence of particular alleles of interest, but does not give a complete MHC class I genotype. In order to determine the full complement of MHC class I genes in each of the three ECs, we prepared cDNA libraries of MHC class I sequences from each animal. We sequenced at least 150 individually cloned cDNAs from these libraries for each EC. This number of clones is typically sufficient to identify the majority, if not all, of the MHC class I alleles expressed in an animal. Screening of the MHC class I cDNA libraries revealed two MHC class I alleles shared by all three ECs: Mamu-B*06 and Mamu-B*08 (Table 1). We had previously determined that Mamu-B*08 encodes a protein detectable by one-dimensional isoelectric focusing (1-D IEF), while Mamu-B*06 does not . It was therefore likely that the restricting element for the two novel epitopes was encoded by Mamu-B*08.
To test the hypothesis that Mamu-B*08 presented the novel epitopes, we next generated CD8+ T cell lines from the three ECs using 15-mer peptides containing the Vif or Nef epitopes. We also stably transfected 721.221 cells ,  with expression constructs for Mamu-B*08 or Mamu-A*01. 721.221 is a human cell line that does not express classical MHC class I molecules, so the only MHC class I molecules on the surface of the transfectants were the products of the transfected constructs. We then asked whether Mamu-B*08 transfectants could present exogenous peptides and elicit cytokine responses detectable in ICS assays. Indeed, CD8+ T cell lines responded at least as strongly to Mamu-B*08-transfectant cells as they did to autologous B-lymphoblastoid cell lines (BLCL) pulsed with either the Vif peptides (Fig. 3A) or the Nef peptides (Fig. 3B). The CD8+ T cell lines did not respond to mismatched Mamu-A*01 transfectants pulsed with the same peptides (Fig. 3A and 3B) or to peptide-pulsed 721.221 cells (data not shown). Taken together, these data indicate that Mamu-B*08 presents the novel epitopes derived from SIV Vif and Nef.
721.221 cells, which do not express endogenous classical MHC class I molecules, were stably transfected with Mamu-B*08 or Mamu-A*01 and pulsed with the appropriate peptides. Peptide-pulsed cells were used in ICS assays with peptide-specific CD8+ T cell lines. CD8+ T cell lines raised against 15-mers derived from A) Vif (positions 165–183) from animal r00078 and B) Nef (positions 133–151) from animal r98016 were stimulated by the Mamu-B*08 stable transfectants pulsed with the relevant peptides. The cytokine reactivity was comparable to levels elicited when autologous BLCL were used as APCs (positive control). No peptide stimulation was observed when using the Mamu-A*01 stable transfectants as APCs (negative control). Negative controls without peptide in the presence of APCs also gave negligible cell stimulation. Percentages over each FACS dot plot signify the maximal cytokine response (total of IFN-γ+ cells, TNF-α+ cells, and IFN-γ+ TNF-α+ cells).
Identification of five more Mamu-B*08-restricted CD8+ T cell epitopes derived from SIVmac239
The Nef epitope we identified, Nef137–146RL10 (RRHRILDIYL), overlapped with a previously identified epitope, Nef136–146AL11 (ARRHRILDIYL), which is restricted by Mamu-B*03 , . Therefore, we compared the amino acid sequences of these two MHC class I molecules to determine whether we could predict a peptide binding motif for Mamu-B*08 extrapolated from the known motif of Mamu-B*03 . Mamu-B*03 and Mamu-B*08 are almost identical in amino acid sequence . There are only two amino acid differences between these molecules in regions that influence peptide binding and antigen recognition , . Both differences reside in the alpha-1 domain (exon 2). Thus, based on these overall structural similarities, analysis of the B and F pockets of Mamu-B*08 in comparison with well-characterized HLA and Mamu specificities, and the sequences of known Mamu-B*03 ,  and the identified Mamu-B*08 epitopes (Figs. 1 and 2), a preliminary Mamu-B*08 peptide binding motif was derived. This preliminary motif specifies the presence of arginine (R) in position 2 (P2) and the aliphatic hydrophobic residues leucine (L), isoleucine (I), or valine (V) at the C-terminus.
We then used the preliminary binding motif to scan SIVmac239 Vif, Nef, and Rev for additional potential Mamu-B*08-restricted epitopes. We focused in particular on these regions because CD8+ T cell populations recognizing these three proteins expanded in r00078, r01064, and r98016 after CD8+ cell depletion (Fig. 4A). We used ELISPOT assays to test the ability of 15-mer peptides containing sequences that fit the motif to stimulate IFN-γ release by PBMC from these three ECs.
MHC class I alleles detected by PCR-SSP are listed for each animal. A) Unknown CD8+ responses from ex vivo ICS assays using SIV peptide pools (containing ten 15-mers overlapping by eleven amino acids) performed one month prior to and four weeks after CD8+ cell depletion. Chronic phase (thirty weeks post-infection) ex vivo ICS data is also shown for responses in r99006 to the seven SIV 15-mer peptide pools that contain the novel CD8+ T cell epitopes. Grayed responses increased >0.1% after CD8+ cell depletion (r00078, r01064, and r98016). B) Ex vivo IFN-γ ELISPOT using one or two overlapping 15-mers containing the minimal optimal Mamu-B*08-restricted SIV-specific epitopes (or the minimal optimal peptide alone, in the case of Vif172–179RL8) demonstrated that these CD8+ responses persist approximately six months post-CD8+ cell depletion in ECs r00078, r01064, and r98016. CD8+ cell responses persist in r99006 at ∼3.5 years post-SIV infection. Mean values and SD from triplicate wells were calculated for each ELISPOT assay. Background (the mean of wells without peptide) levels were subtracted from each well. Mean responses <50 SFC per 1×106 cells were not considered positive because these counts were not significantly above background.
We also determined that an additional animal in the EC cohort, r99006, expressed Mamu-B*08, so this animal was included in further analyses. r99006 was challenged with a recombinant virus bearing escape mutations in Mamu-A*01- and Mamu-B*17-restricted CD8+ T cell epitopes as part of a prior study , . This animal has controlled viremia to <1,000 vRNA copy Eq/ml for over four years post-SIV infection and was not part of the CD8+ cell depletion study. Responses to four peptide pools containing putative Mamu-B*08-restricted epitopes were weakly detectable in ICS assays of r99006 PBMC conducted 30 weeks post-infection (Fig. 4A).
Testing PBMC from all four ECs, we identified another five putative Mamu-B*08-restricted CD8+ T cell epitopes derived from Vif, Nef, and Rev (Fig. 4B). TNF-α and IFN-γ ICS assays using Mamu-B*08 and Mamu-A*01 transfectants confirmed that each of these epitopes was presented by Mamu-B*08 (data not shown). For each Mamu-B*08-restricted response detected by 15-mers, we selected candidate peptides within the 15-mers to define the minimal optimal epitopes. These candidate peptides were chosen on the basis of the preliminary motif and tested in serial dilutions in TNF-α and IFN-γ ICS assays with peptide-specific CD8+ T cell lines as described above for Vif172–179RL8 and Nef137–146RL10 (data not shown). All seven minimal optimal epitopes had an R residue at P2 and L at the C-terminus, in agreement with the putative Mamu-B*08 binding motif (Table 2).
Surprisingly, a majority of the novel Mamu-B*08-restricted CD8+ T cell responses were detected in at least two ECs over 1.5 years after initial infection with SIVmac239 (Fig. 4B). Among these responses, populations recognizing the Nef137–146RL10 epitope appeared dominant or co-dominant in three of four ECs tested. The exception to this pattern was animal r01064, whose Mamu-B*08-restricted response appeared to be dominated by cells responding to an epitope in the C-terminus of Rev, Rev44–51RL8. However, the overlapping Rev 15-mers tested contain not only a Mamu-B*08-restricted CD8+ T cell epitope but also a CD8+ T cell epitope of unknown restriction, which may contribute to the strength of immune responses elicited by this peptide (data not shown). Further experiments suggested that the strong response to the Rev 15-mer we observed in r01064 is due to cells that recognize this unknown epitope (see below).
Staining PBMC with Mamu-B*08 tetrameric complexes reveals the immunodominance hierarchy of Mamu-B*08-restricted CD8+ T cell responses
Having defined seven minimal optimal epitopes bound by Mamu-B*08, we next produced tetrameric complexes of Mamu-B*08 loaded with each of these epitopes. The PCR-SSP-based screen for Mamu-B*08 we developed allowed us to test for the presence of this allele in PBMC from 192 SIVmac239-infected rhesus macaques . Seven animals from this cohort expressed Mamu-B*08: four of these were the previously identified ECs, and three were animals that progressed to AIDS , .
We used the set of Mamu-B*08 tetramers to measure the Mamu-B*08-restricted CD8+ T cell response in archived chronic-phase PBMC from six of these seven SIV-infected macaques. For each epitope, there were detectable tetramer-binding populations of CD8+ T cells in at least two animals (Table 3). In most instances, the frequency of SIV-specific CD8+ T cells against each of the seven novel Mamu-B*08-restricted epitopes was higher in the four EC macaques than the two progressors. Populations recognizing Nef137–146RL10 were dominant in one of the six macaques (r99006), and co-dominant in three more animals with Vif172–179RL8 (r96104) and with Rev12–20KL9 (r98016, r96113). Nef8–16RL9-specific cells were dominant or co-dominant in the remaining two animals (r00078 and r01064). The Nef245–254RL9 was co-dominant with the Nef8–16RL9-specific in r00078.
The high frequency populations detected by Mamu-B*08 Nef137-146RL10 tetramers also confirmed that responses we detected by IFN-γ ELISPOT in four Mamu-B*08-positive ECs were directed against this Mamu-B*08-restricted epitope (Fig. 4B). Indeed, there was general concordance between the immunodominance hierarchy detected by ELISPOT and that measured by tetramers with one exception. In animal r01064 using the Rev44–53RL8 tetramer, we did not detect a CD8+ T cell response (Table 3), although 15-mer peptides containing this sequence elicited the dominant response in ELISPOT assays (Fig. 4B). This result further suggests that the strong response detected in ELISPOT is due to a population that recognizes an epitope not presented by Mamu-B*08.
Mamu-B*08-restricted CD8+ T cells select for viral variation in several SIVmac239 epitopes
To determine whether viral variation in CD8+ T cell epitopes could be associated with expression of Mamu-B*08, we first sequenced vif, rev, and nef ORFs in virus isolated from plasma of chronically infected Mamu-B*08-positive controllers and progressors. We compared the predicted amino acid sequences of the epitope regions and full-length proteins to sequences previously obtained at the time of necropsy from 34 Mamu-B*08-negative MHC-defined macaques infected with SIVmac239 . Strikingly, amino acid substitutions accumulated in each of the seven Mamu-B*08-restricted epitopes we identified in at least two Mamu-B*08-positive macaques (Fig. 5). The substitutions were rarely in residues likely to be crucial for binding to the Mamu-B*08 molecule, P2 or the C-terminus. One exception to this pattern was Vif172–179RL8, in which substitutions affected either P2 or the C-terminus in each animal with epitope mutations. Peptides with P2 glycine (G)-for-arginine (R) substitutions were not recognized by Vif172–179RL8-specific CD8+ T cell lines in ICS assays, supporting the conclusion that these mutations confer escape from Mamu-B*08-restricted CD8+ T cell responses (data not shown).
Viral RNA was isolated from cell-free plasma and directly sequenced. Samples were taken from the time of necropsy for four Mamu-B*08-positive macaques that were sacrificed with progressive SIVmac239 infection (time of necropsy indicated for each animal): r01064 (77 weeks post-CD8+ cell depletion, 129 weeks post-SIV infection), 99C093 (127 weeks post-SIV infection), r96104 (60 weeks post-SIV infection), and r96113 (75 weeks post-SIV infection). Virus was sampled from Mamu-B*08-positive EC r00078 78 weeks post-CD8+ cell depletion (161 weeks post-infection) after viral breakthrough. Virus was sampled from Mamu-B*08-positive EC r98016 during a transient increase in SIV replication at 48 weeks post-CD8+ cell depletion (164 weeks post-infection) during which virus load rose to ∼9,000 vRNA copy Eq/ml before returning to <1,000 copy Eq/ml. Viral sequences from Mamu-B*08-positive animals were compared to sequences obtained at the time of necropsy from 34 Mamu-B*08-negative progressors . The frequency of each sequence detected in these 34 animals is listed in parentheses except for Nef 245–254 where sequences were available from 33 of the 34 animals. Amino acid residues immediately N-terminal to two Nef epitopes are listed and denoted with a space. Those amino acids identical to the wild-type sequence are shown as dots. Complete amino acid replacements are shown in uppercase; sites of mixed-base heterogeneity are shown in lowercase.
In order to examine the effects of selection pressure on Mamu-B*08-restricted epitope sequences more closely, we compared the numbers of nonsynonymous (dN) and synonymous (dS) substitutions per site within epitope-coding regions of vif, rev, and nef with dN and dS for the entire ORFs. This analysis showed that dN was significantly elevated in regions encoding Mamu-B*08-restricted epitopes in animals expressing this molecule (P<0.001, Table 4). Furthermore, dN within the epitope regions was greater in Mamu-B*08-positive than in Mamu-B*08-negative animals (P<0.001), while dS was not significantly different between the groups (Table 4). These results suggest that regions encoding Mamu-B*08-restricted CD8+ T cell epitopes are under selective pressure only in the presence of Mamu-B*08, and thus the variation we detect in Mamu-B*08-restricted epitopes is indeed selected by CD8+ T cell responses.
In one case, substitutions associated with Mamu-B*08 expression occurred not in the epitope sequence, but immediately N-terminal to it. Virus from each of the Mamu-B*08-positive macaques tested had a substitution at Nef residue 136, which is alanine (A) in SIVmac239. The variant sequence encoded a proline (P) at this position (A136P) in five of six animals (Fig. 5). The dN/dS ratio was significantly elevated at this position only in Mamu-B*08-positive animals, indicating strong selection pressure favoring this mutation only in the presence of Mamu-B*08 (data not shown). Since Nef residue 136 is not within the minimal optimal epitope bound by Mamu-B*08, it is possible that A136P affects peptide processing, decreasing the availability of minimal optimal epitopes to Mamu-B*08 molecules. Indeed, a similar A to P substitution immediately N-terminal to the epitope is known to inhibit processing of an HLA-B57-restricted peptide in HIV Gag . At position 136, the A to valine (V) substitution found in EC r98016 is much more conservative and may not alter processing of the epitope. We also detected a substitution one amino acid N-terminal of the minimal optimal Nef246–254RL9 epitope in progressor r96113 (Fig. 5). This was a conservative lysine (K)-for-R substitution, so the impact of this change on peptide processing may be small. This same substitution was also found in two of 33 Mamu-B*08-negative macaques, and relative rates of nonsynonymous and synonymous substitutions were not significantly different in this epitope region in Mamu-B*08-positive and Mamu-B*08-negative animals (data not shown). These data suggest that the R245K substitution is not selected for by Mamu-B*08-restricted CD8+ T cells.
To clarify whether substitutions in Mamu-B*08-restricted epitopes might affect the ability of Mamu-B*08-positive animals to control SIVmac239 infection, we next determined epitope sequences of viruses circulating in Mamu-B*08-positive ECs before and after CD8+ cell depletion, when SIV replication was effectively controlled (Fig. 6). We compared these sequences to those present in virus replicating in the absence of CD8+ T cell selection during the CD8+ cell depletion phase, which we had determined previously . To our surprise, variation in several Mamu-B*08-restricted epitopes was detectable in ECs r98016 and r00078 even before CD8+ cell depletion, when viremia had been successfully controlled to <1,000 vRNA copy Eq/ml for up to two years (Fig. 6). Repeated attempts to amplify viral cDNA from r01064 pre-depletion plasma samples were unsuccessful, likely due to the extremely low concentrations of vRNA in this animal.
Virus was isolated from r00078, r01064, and r98016 at the indicated times before and after CD8+ cell depletion. Pre-depletion samples were obtained one month prior to depleting antibody treatment, when virus loads were <500 vRNA copy Eq/ml. An asterisk (*) indicates a Rev sequence obtained five months prior to CD8+ cell depletion in animal r00078. Pre-depletion sequence from r98016 containing Rev44–51RL8 could not be amplified despite repeated attempts and is listed as n.d. (not done). Viral RNA from pre-depletion plasma samples from r01064 could also not be amplified despite repeated attempts due to low concentrations of vRNA. Viral RNA was isolated from cell-free plasma and analyzed by direct sequencing of viral amplicons spanning the SIV genes vif, rev, and nef. Amino acids residues immediately N-terminal to two Nef epitopes are listed and denoted with a space. Those amino acids identical to the wild-type sequence are shown as dots. Complete amino acid replacements are shown in uppercase; sites of mixed-base heterogeneity are shown as lowercase.
Viral variation was detectable prior to depletion in five of seven identified Mamu-B*08-restricted epitopes in r00078, and in four of six epitopes for which sequence was available in r98016. Mutations present before depletion were still detectable during the peak of virus replication, with three exceptions. Mutations detected in animal r00078 Nef246–254RL9 were not present at peak, although at least one of these mutations, encoding R246K, was detected in the two other ECs' peak virus (Fig. 6). Also in animal r00078, a leucine (L)-for-P substitution was also detected at position five of Nef8–16RL9 before CD8+ cell depletion, but not in the virus replicating in the absence of CD8+ cells. This same substitution reappeared in virus populations isolated at later timepoints, after the return of CD8+ cells. Virus from animal r01064 harbored mutations in the same codon, resulting in a different amino acid substitution (P to glutamine, Q). This change was similarly absent from virus replication during CD8+ cell depletion. In addition, a pre-depletion site of mixed-base heterogeneity N-terminal to Nef137–146RL10 in r98016, encoding A and glutamic acid (E), was fully wild type at the peak of virus replication. In contrast, r00078's virus at position 136 had an A-to-P mutation before, during and after CD8+ cell depletion. These results suggest that commonly detected mutations within these Mamu-B*08-restricted epitopes do not likely exact a heavy cost to viral fitness.
The two Mamu-B*08-positive, Mamu-B*17-negative ECs eventually lost control of viremia, with plasma virus concentrations increasing beyond 1,000 vRNA copy Eq/ml beginning ∼150 days after CD8+ cell depletion treatment. Animal r00078's viremia stabilized at a new plateau level of ∼10,000 vRNA copy Eq/ml by day 300 after depletion, but r01064 had steadily increasing viremia and was sacrificed at day 542 post-depletion with a plasma virus concentration of 1×106 vRNA copy Eq/ml (data not shown). We sequenced plasma virus at two timepoints following this virus breakthrough in both animals to determine whether variation in Mamu-B*08 epitopes could account for their loss of control. Although the patterns of variation were different in each animal, post-breakthrough virus had substitutions that had not been detected immediately after CD8+ cell depletion (Fig. 6). Although we cannot yet determine which substitutions in particular Mamu-B*08-restricted CD8+ T cell epitopes can be correlated with loss of effective viremia control, we were surprised to find that Mamu-B*08-restricted CD8+ T cell responses appeared to select for viral variation in all identified epitopes in the majority of animals.
In a recent study aimed at identifying correlates of EC of SIV replication, we transiently depleted CD8+ cells from the periphery in six macaque ECs . Four of these animals expressed Mamu-B*17, which we had previously shown to be associated with a reduction in chronic phase viremia in a large cohort of SIVmac239-infected macaques . In that study, we found that particular epitope-specific populations of CD8+ T cells expanded dramatically as CD8+ cells repopulated the periphery and control of virus replication was re-established. In the Mamu-B*17-positive animals these expanding populations frequently targeted previously described Mamu-B*17-restricted epitopes in Vif and Nef. To our surprise, the Mamu-B*17-negative animals in that study also had expanding populations of CD8+ T cells that targeted Vif and Nef (Figs. 1 and 2). Because these populations showed a substantial expansion as control of SIV replication was re-asserted, we speculate that they played an important role in this control.
Here we show that these expanding CD8+ T cell populations in the Mamu-B*17-negative macaques recognized novel epitopes bound by the MHC class I molecule Mamu-B*08 (Fig. 3). Indeed, Mamu-B*08 presents at least seven epitopes derived from SIVmac239 to CD8+ T cells (Table 2) and is expressed in three of the six ECs in our CD8+ cell depletion study, including both Mamu-B*17-negative ECs. We recently reported that Mamu-B*08 was enriched in a cohort of EC macaques and is associated with reduced chronic phase viremia in SIVmac239-infected rhesus macaques , further indicating that Mamu-B*08-restricted CD8+ T cell responses play an important role in controlling SIV replication. Using cytokine secretion assays and synthesizing Mamu-B*08 tetramers, we found strong responses to the newly defined epitopes in chronically infected ECs, even when viremia was low. Among the newly identified epitopes were two derived from SIVmac239 Rev, Rev12-20KL9 and Rev44-51RL8. These are the first MHC class I minimal optimal epitopes described in SIV Rev.
Cytokine secretion assays and MHC class I tetramer stains also allowed us to identify immunodominance hierarchies among Mamu-B*08-restricted CD8+ T cell populations (Fig. 4 and Table 3). Nef137–146RL10-specific CD8+ T cells were dominant or co-dominant as detected by MHC class I tetramers in four of six Mamu-B*08-positive animals in the chronic phase of SIV infection. Strong IFN-γ responses to Nef137–146RL10-containing peptides were also detected in all four Mamu-B*08-positive ECs. CD8+ T cell populations responding to Rev or Vif epitopes were co-dominant with or subdominant to these Nef137-146RL10-specific populations in the three ECs.
Sequencing of vif, rev, and nef ORFs revealed that Mamu-B*08-restricted CD8+ T cells exert selective pressure on a surprisingly broad scale. All seven epitopes we identified had substitutions in at least two of seven chronically SIV-infected Mamu-B*08-positive animals (Fig. 5). Substitutions within the dominant Nef137–146RL10 epitope sequence were infrequent in these animals, but a mutation one codon upstream of the epitope (encoding A136P) occurred in six of seven Mamu-B*08-positive animals. A study of HIV-infected patients showed that viruses bearing a similar alanine-to-proline substitution immediately N-terminal of an HLA-B57-restricted Gag epitope were not recognized by epitope-specific CTL . In that case, the A-to-P mutation altered processing of the epitope peptide, decreasing its availability for loading onto HLA-B57. It is possible that the A136P substitutions we observed in Nef similarly alter processing of the Mamu-B*08-restricted epitope peptide. We detected evidence for positive selection pressure on Mamu-B*08-restricted CD8+ T cell epitopes associated with expression of Mamu-B*08 (Table 4). Therefore, it is likely that these substitutions represent viral escape from Mamu-B*08-restricted CD8+ T cell responses. Viral escape in particular CD8+ T cell epitopes has previously been correlated with a loss of effective immune containment of viremia in HLA-B27-positive humans and Mamu-A*01-positive macaques , , –. In our study, it was difficult to correlate particular epitope substitutions with the eventual loss of control of viral replication in two CD8+ cell-depleted Mamu-B*08-positive ECs (Fig. 6).
It is thought that individuals with “elite” control of HIV infection provide an important and all-too-rare example of successful host responses to the virus. Although these individuals have been studied for at least ten years, the mechanisms of control have been extremely difficult to define. Expression of particular MHC class I alleles, particularly HLA-B27 and -B57, has been associated with elite control of HIV infection –. It seems reasonable to infer from this association that certain HLA-B27- and HLA-B57-restricted epitope-specific CD8+ T cells are particularly effective at controlling virus replication. But so far, with the possible exception of the HLA-B27-restricted epitope Gag263-272KK10, no candidate “controller” responses have been identified. MHC class I alleles may exert their protective effects through additional, as yet unknown, means.
Animal models of MHC class I-associated elite control of immunodeficiency virus replication could therefore offer a valuable tool for studying the mechanisms of control. We have previously shown that Mamu-B*17 is over-represented in a cohort of SIVmac239 ECs . Recently, we discovered that Mamu-B*08 expression is associated with a reduction in chronic phase viremia of a similar magnitude to that seen for Mamu-B*17 . Interestingly, the peptide binding motif of Mamu-B*17 is broadly similar to that of HLA-B57. Although Mamu-B*17 seems to tolerate a wider array of residues at P2, both molecules exhibit a preference for W, F, or Y at the C-terminus , , . At the same time, a preliminary binding motif for Mamu-B*08, defined on the basis of structural analyses, is similar to that defined for HLA-B27 , , , . All seven Mamu-B*08-restricted CD8+ T cell epitopes we identified contained R at position 2 and L at the C-terminus, which also fits the HLA-B27 motif. Indeed, a recent study has provided evidence that this P2 requirement for R, a long, basic residue, may result in some unusual peptide binding and presentation characteristics for HLA-B27. Peptides with a dibasic N-terminal motif were relatively resistant to degradation by cytosolic aminopeptidases, resulting in an over-representation of peptides with the N-terminal motif KR or RR in the HLA-B27 peptidome . The authors of that study suggested that because HLA-B27 “selects” ligands that are particularly stable in the cytosol. It therefore may require fewer molecules of viral peptides than other HLA class I molecules to trigger a response from CD8+ T cells. This might help explain the apparent effectiveness of HLA-B27-restricted CD8+ T cell responses against HIV. Since Mamu-B*08 shares the peptide-binding characteristics of HLA-B27, it may similarly restrict CD8+ T cells capable of recognizing infected cells even when cytosolic virus-derived peptide concentrations are low, for example immediately after infection, or in latent infection.
As the HIV pandemic progresses, so does the urgent need for an AIDS vaccine. Although there is broad agreement that CD8+ T cell responses will be an important component of vaccine-induced immunity, the attributes of effective antiviral CD8+ T cells are still unknown. Since they appear naturally to make effective immune responses, ECs, both macaque and human, provide an important example of what is possible. Here we report a new model of elite control of immunodeficiency virus infection, Mamu-B*08-positive macaques that effectively control infection with the pathogenic clone SIVmac239. It will be important in future studies to refine the Mamu-B*08 peptide binding motif, to identify all of the SIV-derived epitopes bound by this molecule, and to test the efficacy of Mamu-B*08-restricted CD8+ T cells more directly. Interestingly, Mamu-B*08-associated control of SIVmac239 replication may closely parallel HLA-B27-associated control of HIV replication.
We thank William Rehrauer, Chrystal Glidden, Gretta Borchardt, and Debi Fisk for MHC class I PCR-SSP typing. We gratefully acknowledge Gnankang Napoé and Jason Reed for the construction of MHC class I tetramers, and Alex Blasky for assistance with DNA sequencing. Laura Valentine, Nicholas Maness, and Bjoern Peters provided helpful discussions. We also thank the Virology, Genetics, Immunology, and Animal core laboratories as well as Research Support Services at the National Primate Research Center, University of Wisconsin-Madison (WNPRC) for technical assistance.
The following reagents were obtained through the NIH AIDS Research and Reference Reagent Program, Division of AIDS, NIAID, NIH: IL-2, human (item #136) from Hoffman-La Roche, Inc. as well as complete SIVmac239 peptide sets (15-mers overlapping by eleven amino acids) of Gag (item #6204), Vif (item #6205), Tat (item #6207), Pol (item #6443), Rev (item #6448), Vpr (item #6449), Vpx (item #6450), Env (item #6883), and full length Nef (item #8762) from DAIDS, NIAID.
Conceived and designed the experiments: DW JL TF. Performed the experiments: JL EL JS DR SS AB DB BB RR LW SP GM. Analyzed the data: JS AH JL TF EL DR SS AB DB RR LW SP GM HP. Contributed reagents/materials/analysis tools: AS DP EG EK NW. Wrote the paper: DW JL TF.
- 1. Borrow P, Lewicki H, Hahn BH, Shaw GM, Oldstone MB (1994) Virus-specific CD8+ cytotoxic T-lymphocyte activity associated with control of viremia in primary human immunodeficiency virus type 1 infection. J Virol 68: 6103–6110.
- 2. Koup RA, Safrit JT, Cao Y, Andrews CA, McLeod G, et al. (1994) Temporal association of cellular immune responses with the initial control of viremia in primary human immunodeficiency virus type 1 syndrome. J Virol 68: 4650–4655.
- 3. Reimann KA, Tenner-Racz K, Racz P, Montefiori DC, Yasutomi Y, et al. (1994) Immunopathogenic events in acute infection of rhesus monkeys with simian immunodeficiency virus of macaques. J Virol 68: 2362–2370.
- 4. Kuroda MJ, Schmitz JE, Charini WA, Nickerson CE, Lifton MA, et al. (1999) Emergence of CTL coincides with clearance of virus during primary simian immunodeficiency virus infection in rhesus monkeys. J Immunol 162: 5127–5133.
- 5. Li Q, Duan L, Estes JD, Ma ZM, Rourke T, et al. (2005) Peak SIV replication in resting memory CD4+ T cells depletes gut lamina propria CD4+ T cells. Nature 434: 1148–1152.
- 6. Mattapallil JJ, Douek DC, Hill B, Nishimura Y, Martin M, et al. (2005) Massive infection and loss of memory CD4+ T cells in multiple tissues during acute SIV infection. Nature 434: 1093–1097.
- 7. Kaslow RA, Carrington M, Apple R, Park L, Munoz A, et al. (1996) Influence of combinations of human major histocompatibility complex genes on the course of HIV-1 infection. Nat Med 2: 405–411.
- 8. Carrington M, Nelson GW, Martin MP, Kissner T, Vlahov D, et al. (1999) HLA and HIV-1: heterozygote advantage and B*35-Cw*04 disadvantage. Science 283: 1748–1752.
- 9. Hendel H, Caillat-Zucman S, Lebuanec H, Carrington M, O'Brien S, et al. (1999) New class I and II HLA alleles strongly associated with opposite patterns of progression to AIDS. J Immunol 162: 6942–6946.
- 10. Migueles SA, Sabbaghian MS, Shupert WL, Bettinotti MP, Marincola FM, et al. (2000) HLA B*5701 is highly associated with restriction of virus replication in a subgroup of HIV-infected long term nonprogressors. Proc Natl Acad Sci U S A 97: 2709–2714.
- 11. Carrington M, O'Brien SJ (2003) The influence of HLA genotype on AIDS. Annu Rev Med 54: 535–551.
- 12. Keet IP, Tang J, Klein MR, LeBlanc S, Enger C, et al. (1999) Consistent associations of HLA class I and II and transporter gene products with progression of human immunodeficiency virus type 1 infection in homosexual men. J Infect Dis 180: 299–309.
- 13. Pal R, Venzon D, Letvin NL, Santra S, Montefiori DC, et al. (2002) ALVAC-SIV-gag-pol-env-based vaccination and macaque major histocompatibility complex class I (A*01) delay simian immunodeficiency virus SIVmac-induced immunodeficiency. J Virol 76: 292–302.
- 14. Zhang ZQ, Fu TM, Casimiro DR, Davies ME, Liang X, et al. (2002) Mamu-A*01 allele-mediated attenuation of disease progression in simian-human immunodeficiency virus infection. J Virol 76: 12845–12854.
- 15. Muhl T, Krawczak M, Ten Haaft P, Hunsmann G, Sauermann U (2002) MHC class I alleles influence set-point viral load and survival time in simian immunodeficiency virus-infected rhesus monkeys. J Immunol 169: 3438–3446.
- 16. O'Connor DH, Mothe BR, Weinfurter JT, Fuenger S, Rehrauer WM, et al. (2003) Major histocompatibility complex class I alleles associated with slow simian immunodeficiency virus disease progression bind epitopes recognized by dominant acute-phase cytotoxic-T-lymphocyte responses. J Virol 77: 9029–9040.
- 17. Yant LJ, Friedrich TC, Johnson RC, May GE, Maness NJ, et al. (2006) The high-frequency major histocompatibility complex class I allele Mamu-B*17 is associated with control of simian immunodeficiency virus SIVmac239 replication. J Virol 80: 5074–5077.
- 18. Phillips RE, Rowland-Jones S, Nixon DF, Gotch FM, Edwards JP, et al. (1991) Human immunodeficiency virus genetic variation that can escape cytotoxic T cell recognition. Nature 354: 453–459.
- 19. Koenig S, Conley AJ, Brewah YA, Jones GM, Leath S, et al. (1995) Transfer of HIV-1-specific cytotoxic T lymphocytes to an AIDS patient leads to selection for mutant HIV variants and subsequent disease progression. Nat Med 1: 330–336.
- 20. Borrow P, Lewicki H, Wei X, Horwitz MS, Peffer N, et al. (1997) Antiviral pressure exerted by HIV-1-specific cytotoxic T lymphocytes (CTLs) during primary infection demonstrated by rapid selection of CTL escape virus. Nat Med 3: 205–211.
- 21. Goulder PJ, Phillips RE, Colbert RA, McAdam S, Ogg G, et al. (1997) Late escape from an immunodominant cytotoxic T-lymphocyte response associated with progression to AIDS. Nat Med 3: 212–217.
- 22. Evans DT, O'Connor DH, Jing P, Dzuris JL, Sidney J, et al. (1999) Virus-specific cytotoxic T-lymphocyte responses select for amino-acid variation in simian immunodeficiency virus Env and Nef. Nat Med 5: 1270–1276.
- 23. Allen TM, O'Connor DH, Jing P, Dzuris JL, Mothe BR, et al. (2000) Tat-specific cytotoxic T lymphocytes select for SIV escape variants during resolution of primary viraemia. Nature 407: 386–390.
- 24. Barouch DH, Kunstman J, Kuroda MJ, Schmitz JE, Santra S, et al. (2002) Eventual AIDS vaccine failure in a rhesus monkey by viral escape from cytotoxic T lymphocytes. Nature 415: 335–339.
- 25. O'Connor DH, Allen TM, Vogel TU, Jing P, DeSouza IP, et al. (2002) Acute phase cytotoxic T lymphocyte escape is a hallmark of simian immunodeficiency virus infection. Nat Med 8: 493–499.
- 26. Allen TM, Altfeld M, Geer SC, Kalife ET, Moore C, et al. (2005) Selective escape from CD8+ T-cell responses represents a major driving force of human immunodeficiency virus type 1 (HIV-1) sequence diversity and reveals constraints on HIV-1 evolution. J Virol 79: 13239–13249.
- 27. Price DA, Goulder PJ, Klenerman P, Sewell AK, Easterbrook PJ, et al. (1997) Positive selection of HIV-1 cytotoxic T lymphocyte escape variants during primary infection. Proc Natl Acad Sci U S A 94: 1890–1895.
- 28. Jin X, Bauer DE, Tuttleton SE, Lewin S, Gettie A, et al. (1999) Dramatic rise in plasma viremia after CD8(+) T cell depletion in simian immunodeficiency virus-infected macaques. J Exp Med 189: 991–998.
- 29. Matano T, Shibata R, Siemon C, Connors M, Lane HC, et al. (1998) Administration of an anti-CD8 monoclonal antibody interferes with the clearance of chimeric simian/human immunodeficiency virus during primary infections of rhesus macaques. J Virol 72: 164–169.
- 30. Schmitz JE, Kuroda MJ, Santra S, Sasseville VG, Simon MA, et al. (1999) Control of viremia in simian immunodeficiency virus infection by CD8+ lymphocytes. Science 283: 857–860.
- 31. Deeks SG, Walker BD (2007) Human immunodeficiency virus controllers: mechanisms of durable virus control in the absence of antiretroviral therapy. Immunity 27: 406–416.
- 32. Alexander L, Weiskopf E, Greenough TC, Gaddis NC, Auerbach MR, et al. (2000) Unusual polymorphisms in human immunodeficiency virus type 1 associated with nonprogressive infection. J Virol 74: 4361–4376.
- 33. Lum JJ, Cohen OJ, Nie Z, Weaver JG, Gomez TS, et al. (2003) Vpr R77Q is associated with long-term nonprogressive HIV infection and impaired induction of apoptosis. J Clin Invest 111: 1547–1554.
- 34. Rhodes DI, Ashton L, Solomon A, Carr A, Cooper D, et al. (2000) Characterization of three nef-defective human immunodeficiency virus type 1 strains associated with long-term nonprogression. Australian Long-Term Nonprogressor Study Group. J Virol 74: 10581–10588.
- 35. Salvi R, Garbuglia AR, Di Caro A, Pulciani S, Montella F, et al. (1998) Grossly defective nef gene sequences in a human immunodeficiency virus type 1-seropositive long-term nonprogressor. J Virol 72: 3646–3657.
- 36. Ioannidis JP, Rosenberg PS, Goedert JJ, Ashton LJ, Benfield TL, et al. (2001) Effects of CCR5-Delta32, CCR2-64I, and SDF-1 3'A alleles on HIV-1 disease progression: An international meta-analysis of individual-patient data. Ann Intern Med 135: 782–795.
- 37. Liu H, Hwangbo Y, Holte S, Lee J, Wang C, et al. (2004) Analysis of genetic polymorphisms in CCR5, CCR2, stromal cell-derived factor-1, RANTES, and dendritic cell-specific intercellular adhesion molecule-3-grabbing nonintegrin in seronegative individuals repeatedly exposed to HIV-1. J Infect Dis 190: 1055–1058.
- 38. Liu R, Paxton WA, Choe S, Ceradini D, Martin SR, et al. (1996) Homozygous defect in HIV-1 coreceptor accounts for resistance of some multiply-exposed individuals to HIV-1 infection. Cell 86: 367–377.
- 39. Martin MP, Dean M, Smith MW, Winkler C, Gerrard B, et al. (1998) Genetic acceleration of AIDS progression by a promoter variant of CCR5. Science 282: 1907–1911.
- 40. Soriano A, Martinez C, Garcia F, Plana M, Palou E, et al. (2002) Plasma stromal cell-derived factor (SDF)-1 levels, SDF1-3'A genotype, and expression of CXCR4 on T lymphocytes: their impact on resistance to human immunodeficiency virus type 1 infection and its progression. J Infect Dis 186: 922–931.
- 41. Barassi C, Lazzarin A, Lopalco L (2004) CCR5-specific mucosal IgA in saliva and genital fluids of HIV-exposed seronegative subjects. Blood 104: 2205–2206.
- 42. Pastori C, Weiser B, Barassi C, Uberti-Foppa C, Ghezzi S, et al. (2006) Long-lasting CCR5 internalization by antibodies in a subset of long-term nonprogressors: a possible protective effect against disease progression. Blood 107: 4825–4833.
- 43. Harrer T, Harrer E, Kalams SA, Barbosa P, Trocha A, et al. (1996) Cytotoxic T lymphocytes in asymptomatic long-term nonprogressing HIV-1 infection. Breadth and specificity of the response and relation to in vivo viral quasispecies in a person with prolonged infection and low viral load. J Immunol 156: 2616–2623.
- 44. Harrer T, Harrer E, Kalams SA, Elbeik T, Staprans SI, et al. (1996) Strong cytotoxic T cell and weak neutralizing antibody responses in a subset of persons with stable nonprogressing HIV type 1 infection. AIDS Res Hum Retroviruses 12: 585–592.
- 45. Betts MR, Nason MC, West SM, De Rosa SC, Migueles SA, et al. (2006) HIV nonprogressors preferentially maintain highly functional HIV-specific CD8+ T cells. Blood 107: 4781–4789.
- 46. Horton H, Frank I, Baydo R, Jalbert E, Penn J, et al. (2006) Preservation of T cell proliferation restricted by protective HLA alleles is critical for immune control of HIV-1 infection. J Immunol 177: 7406–7415.
- 47. Lichterfeld M, Kaufmann DE, Yu XG, Mui SK, Addo MM, et al. (2004) Loss of HIV-1-specific CD8+ T cell proliferation after acute HIV-1 infection and restoration by vaccine-induced HIV-1-specific CD4+ T cells. J Exp Med 200: 701–712.
- 48. Migueles SA, Laborico AC, Shupert WL, Sabbaghian MS, Rabin R, et al. (2002) HIV-specific CD8+ T cell proliferation is coupled to perforin expression and is maintained in nonprogressors. Nat Immunol 3: 1061–1068.
- 49. Betts MR, Exley B, Price DA, Bansal A, Camacho ZT, et al. (2005) Characterization of functional and phenotypic changes in anti-Gag vaccine-induced T cell responses and their role in protection after HIV-1 infection. Proc Natl Acad Sci U S A 102: 4512–4517.
- 50. Goulder PJ, Brander C, Tang Y, Tremblay C, Colbert RA, et al. (2001) Evolution and transmission of stable CTL escape mutations in HIV infection. Nature 412: 334–338.
- 51. Feeney ME, Tang Y, Roosevelt KA, Leslie AJ, McIntosh K, et al. (2004) Immune escape precedes breakthrough human immunodeficiency virus type 1 viremia and broadening of the cytotoxic T-lymphocyte response in an HLA-B27-positive long-term-nonprogressing child. J Virol 78: 8927–8930.
- 52. Migueles SA, Laborico AC, Imamichi H, Shupert WL, Royce C, et al. (2003) The differential ability of HLA B*5701+ long-term nonprogressors and progressors to restrict human immunodeficiency virus replication is not caused by loss of recognition of autologous viral gag sequences. J Virol 77: 6889–6898.
- 53. Mao H, Lafont BA, Igarashi T, Nishimura Y, Brown C, et al. (2005) CD8+ and CD20+ lymphocytes cooperate to control acute simian immunodeficiency virus/human immunodeficiency virus chimeric virus infections in rhesus monkeys: modulation by major histocompatibility complex genotype. J Virol 79: 14887–14898.
- 54. Loffredo JT, Maxwell J, Qi Y, Glidden CE, Borchardt GJ, et al. (2007) Mamu-B*08-positive macaques control simian immunodeficiency virus replication. J Virol 81: 8827–8832.
- 55. Friedrich TC, Valentine LE, Yant LJ, Rakasz EG, Piaskowski SM, et al. (2007) Subdominant CD8+ T-cell responses are involved in durable control of AIDS virus replication. J Virol 81: 3465–3476.
- 56. Loffredo JT, Sidney J, Piaskowski S, Szymanski A, Furlott J, et al. (2005) The high frequency Indian rhesus macaque MHC class I molecule, Mamu-B*01, does not appear to be involved in CD8+ T lymphocyte responses to SIVmac239. J Immunol 175: 5986–5997.
- 57. Kaizu M, Borchardt GJ, Glidden CE, Fisk DL, Loffredo JT, et al. (2007) Molecular typing of major histocompatibility complex class I alleles in the Indian rhesus macaque which restrict SIV CD8(+) T cell epitopes. Immunogenetics 59: 693–703.
- 58. Kestler H, Kodama T, Ringler D, Marthas M, Pedersen N, et al. (1990) Induction of AIDS in rhesus monkeys by molecularly cloned simian immunodeficiency virus. Science 248: 1109–1112.
- 59. Friedrich TC, Dodds EJ, Yant LJ, Vojnov L, Rudersdorf R, et al. (2004) Reversion of CTL escape-variant immunodeficiency viruses in vivo. Nat Med 10: 275–281.
- 60. Friedrich TC, McDermott AB, Reynolds MR, Piaskowski S, Fuenger S, et al. (2004) Consequences of cytotoxic T-lymphocyte escape: common escape mutations in simian immunodeficiency virus are poorly recognized in naive hosts. J Virol 78: 10064–10073.
- 61. Cline AN, Bess JW, Piatak M Jr, Lifson JD (2005) Highly sensitive SIV plasma viral load assay: practical considerations, realistic performance expectations, and application to reverse engineering of vaccines for AIDS. J Med Primatol 34: 303–312.
- 62. Loffredo JT, Burwitz BJ, Rakasz EG, Spencer SP, Stephany JJ, et al. (2007) The antiviral efficacy of simian immunodeficiency virus-specific CD8+ T cells is unrelated to epitope specificity and is abrogated by viral escape. J Virol 81: 2624–2634.
- 63. Vogel TU, Friedrich TC, O'Connor DH, Rehrauer W, Dodds EJ, et al. (2002) Escape in one of two cytotoxic T-lymphocyte epitopes bound by a high-frequency major histocompatibility complex class I molecule, Mamu-A*02: a paradigm for virus evolution and persistence? J Virol 76: 11623–11636.
- 64. Loffredo JT, Sidney J, Wojewoda C, Dodds E, Reynolds MR, et al. (2004) Identification of seventeen new simian immunodeficiency virus-derived CD8+ T cell epitopes restricted by the high frequency molecule, Mamu-A*02, and potential escape from CTL recognition. J Immunol 173: 5064–5076.
- 65. Hutchinson SL, Wooldridge L, Tafuro S, Laugel B, Glick M, et al. (2003) The CD8 T cell coreceptor exhibits disproportionate biological activity at extremely low binding affinities. J Biol Chem 278: 24285–24293.
- 66. Shimizu Y, Koller B, Geraghty D, Orr H, Shaw S, et al. (1986) Transfer of cloned human class I major histocompatibility complex genes into HLA mutant human lymphoblastoid cells. Mol Cell Biol 6: 1074–1087.
- 67. Evans DT, Jing P, Allen TM, O'Connor DH, Horton H, et al. (2000) Definition of five new simian immunodeficiency virus cytotoxic T-lymphocyte epitopes and their restricting major histocompatibility complex class I molecules: evidence for an influence on disease progression. J Virol 74: 7400–7410.
- 68. O'Connor DH, McDermott AB, Krebs KC, Dodds EJ, Miller JE, et al. (2004) A dominant role for CD8+-T-lymphocyte selection in simian immunodeficiency virus sequence variation. J Virol 78: 14012–14022.
- 69. Nei M, Gojobori T (1986) Simple methods for estimating the numbers of synonymous and nonsynonymous nucleotide substitutions. Mol Biol Evol 3: 418–426.
- 70. Hughes AL, Piontkivska H, Krebs KC, O'Connor DH, Watkins DI (2005) Within-host evolution of CD8+-TL epitopes encoded by overlapping and non-overlapping reading frames of simian immunodeficiency virus. Bioinformatics 21 Suppl 3: iii39–iii44.
- 71. Hughes AL, Friedman R, Glenn NL (2006) The Future of Data Analysis in Evolutionary Genomics. Current Genomics 7: 227–234.
- 72. Robinson S, Charini WA, Newberg MH, Kuroda MJ, Lord CI, et al. (2001) A commonly recognized simian immunodeficiency virus Nef epitope presented to cytotoxic T lymphocytes of Indian-origin rhesus monkeys by the prevalent major histocompatibility complex class I allele Mamu-A*02. J Virol 75: 10179–10186.
- 73. Mothe BR, Sidney J, Dzuris JL, Liebl ME, Fuenger S, et al. (2002) Characterization of the peptide-binding specificity of Mamu-B*17 and identification of Mamu-B*17-restricted epitopes derived from simian immunodeficiency virus proteins. J Immunol 169: 210–219.
- 74. Boyson JE, Shufflebotham C, Cadavid LF, Urvater JA, Knapp LA, et al. (1996) The MHC class I genes of the rhesus monkey. Different evolutionary histories of MHC class I and II genes in primates. J Immunol 156: 4656–4665.
- 75. Dzuris JL, Sidney J, Appella E, Chesnut RW, Watkins DI, et al. (2000) Conserved MHC class I peptide binding motif between humans and rhesus macaques. J Immunol 164: 283–291.
- 76. Bjorkman PJ, Saper MA, Samraoui B, Bennett WS, Strominger JL, et al. (1987) The foreign antigen binding site and T cell recognition regions of class I histocompatibility antigens. Nature 329: 512–518.
- 77. Garrett TP, Saper MA, Bjorkman PJ, Strominger JL, Wiley DC (1989) Specificity pockets for the side chains of peptide antigens in HLA-Aw68. Nature 342: 692–696.
- 78. Draenert R, Le Gall S, Pfafferott KJ, Leslie AJ, Chetty P, et al. (2004) Immune selection for altered antigen processing leads to cytotoxic T lymphocyte escape in chronic HIV-1 infection. J Exp Med 199: 905–915.
- 79. Rammensee H, Bachmann J, Emmerich NP, Bachor OA, Stevanovic S (1999) SYFPEITHI: database for MHC ligands and peptide motifs. Immunogenetics 50: 213–219.
- 80. Marsh SGE, Parham P, Barber LD (2000) The HLA Facts Book. San Diego: Academic Press.
- 81. Herberts CA, Neijssen JJ, de Haan J, Janssen L, Drijfhout JW, et al. (2006) Cutting edge: HLA-B27 acquires many N-terminal dibasic peptides: coupling cytosolic peptide stability to antigen presentation. J Immunol 176: 2697–2701.
- 82. Allen TM, Mothe BR, Sidney J, Jing P, Dzuris JL, et al. (2001) CD8(+) lymphocytes from simian immunodeficiency virus-infected rhesus macaques recognize 14 different epitopes bound by the major histocompatibility complex class I molecule mamu-A*01: implications for vaccine design and testing. J Virol 75: 738–749.