Figures
Abstract
Background
Although several studies have investigated whether CCL3L1 copy number variation (CNV) influences the risk of HIV-1 infection, there are still no clear conclusions. Therefore, we performed a meta-analysis using two models to generate a more robust estimate of the association between CCL3L1 CNV and susceptibility to HIV-1 infection.
Methods
We divided the cases and controls into two parts as individuals with CCL3L1 gene copy number (GCN) above the population specific median copy number (PMN) and individuals with CCL3L1 GCN below PMN, respectively. Odds ratios (ORs) with 95% confidence intervals (95% CIs) were given for the main analysis. We also conducted stratified analyses by ethnicity, age group and sample size. Relevant literatures were searched through PubMed and ISI Web of Knowledge up to March 2010.
Results
In total, 9 studies with 2434 cases and 4029 controls were included. ORs for the main analysis were 1.35 (95% CI, 1.02–1.78, model: GCN ≤ PMN Vs. GCN > PMN) and 1.70 (95% CI, 1.30–2.23, model: GCN < PMN Vs. GCN ≥ PMN), respectively. Either in stratified analysis, statistically significant results can be detected in some subgroups.
Citation: Liu S, Yao L, Ding D, Zhu H (2010) CCL3L1 Copy Number Variation and Susceptibility to HIV-1 Infection: A Meta-Analysis. PLoS ONE 5(12): e15778. https://doi.org/10.1371/journal.pone.0015778
Editor: Derya Unutmaz, New York University, United States of America
Received: September 30, 2010; Accepted: November 28, 2010; Published: December 30, 2010
Copyright: © 2010 Liu 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 work was supported by National Grand Program on Key Infectious Disease (2008ZX10001-006), National Natural Science Funding of China (No.30972609), Basic Science Key Program of Shanghai (No.08JC1401300) and National Talent Training Fund in Basic Research of China (No. J1030627). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Introduction
Before 2009 acquired immunodeficiency syndrome (AIDS) has took over 25 million people's life, which have exceeded the death toll of the First World War. What is worse, nearly 33 million people suffered from HIV-1 infection [1]. It has been generally accepted that genetic variants among individuals can regulate HIV-1 cell entry, immune response and other factors that influence the susceptibility to HIV-1 infection, disease progressing and curative effects [2], [3]. Recently, CCL3L1 (human CC chemokine ligand 3-like 1) is recognized as one of the important genetic factors for HIV-1 infection.
CCL3L1, also known as macrophage-inflammatory protein 1α(MIP-1α), locates on chromosome 17q11.2 with clusters of cytokine genes. It can bind to several chemokine receptors including CCR5, which is one of the most important co-receptors for HIV-1 [4]. Binding of CCL3L1 to CCR5 may psychically block HIV-1 entry into cells by inhabiting the requisite co-receptor and suppress HIV viral replication in vitro [5]. Thus genetic variations among individuals that regulate the expression of CCL3L1 may influence susceptibility to HIV-1 infection.
CCL3L1 is highly variable in its copy number owing to having a hot spot for segmental duplications in the human genome [6]. Most individuals have 1 to 6 copies per diploid genome, while few individuals have 0 or more than 6 copies. Africans have larger copy number of CCL3L1 than non-Africans [4].
Recently, several studies reported that CCL3L1 CNV is tightly linked to HIV-1 susceptibility and processing a lower copy number of CCL3L1 in the geographic ancestral population is associated with increased risk of HIV-1 infection [7]–[12], whereas other studies didn't suggest this result [13]–[16]. Hence, we performed this meta-analysis of eligible studies to explore a more robust estimate of the association between CCL3L1 CNV and susceptibility to HIV-1 infection.
Materials and Methods
Literature research
Literatures were screened through PubMed and ISI Web of Knowledge up to March 2010, using the key words HIV-1, susceptibility, CCL3L1, MIP-1α in various combinations. Titles and/or abstracts were screened to estimate relevance of investigations. Full texts of primary selected literatures were downloaded for further study. Their references were hand-searched for potential related investigations. Articles were restricted to English language.
Inclusion and exclusion criteria
The included investigations must accord with the following criteria: (1) Case-control studies reporting the association of CCL3L1 CNV and HIV-1 susceptibility; (2) Containing data of distribution of CCL3L1 GCN among the cohorts; (3) Published with English language. Major exclusion criteria as: (1) No sufficient data of CCL3L1 GCN distribution among the cohorts; (2) Reviews; (3) Duplication of previous studies.
Data extraction and statistical analysis
One author (Liu) searched for eligible investigations according to the inclusion and exclusion criteria listed above. Study characteristics including authors, countries, year of publication, ethnicity, sample size of cohorts, distribution of CCL3L1 GCN among the cohorts were extracted by 2 authors (Liu and Yao) independently.
Crude ORs with 95% CIs were calculated to access the association of CCL3L1 CNV and HIV-1 susceptibility. Two genetic models were applied to analyse the distribution of CCL3L1 GCN among the cohorts. In the GCN ≤ PMN Vs. GCN > PMN model, cases and controls were divided into two parts as subjects with CCL3L1 GCN ≤ PMN and subjects with CCL3L1 GCN> PMN, respectively. And in the GCN < PMN Vs. GCN ≥ PMN model, cases and controls were divided into two parts as subjects with CCL3L1 GCN < PMN and subjects with CCL3L1 GCN ≥ PMN, respectively. Stratified analyses were performed by ethnicity, age group and sample size. Heterogeneity across studies was assessed with chi-square-based Q-test [17] and was considered significant if p<0.10, then the data were combined basing on the random-effects (Dersimonian and Laird) model [18]; otherwise the fixed-effects (Mantel and Haenszel) model was applied [19]. Publication bias was evaluated by Egger's and Begg's tests with visual inspection of funnel plots and was considered significant if p<0.05 [20], [21]. One-way sensitivity analyses were performed to examine the influence of individual studies on meta-analysis's results [22]. STATA version 10.0 (Stata Corporation, College station, TX) was used for all analyses.
Results
Figure 1 indicates the selection process of literatures. We have 46 records searched through PubMed and ISI Web of Knowledge. After screening over titles and/or abstracts, full texts were obtained from the remaining 21 articles for further analysis [6]–[17], [23]–[32]. Among them 5 reviews were excluded [6], [24], [28], [30], [32], 1 study was excluded for its study object wasn't human being [26], 4 studies were excluded due to improper study direction (not aimed at the association of CCL3L1 CNV and HIV-1 susceptibility) [25], [27], [29], [31]. During the extraction of data, 2 studies were excluded due to insufficient data of CCL3L1 GCN distribution among the cohorts [13], [17].
Nine studies, involving 2434 HIV-1 infected patients and 4029 HIV-1 uninfected healthy donors, were included in this meta-analysis. Study sample size ranged from 120 to 3173 subjects. Study characteristics of the 9 eligible studies are summarized in Table S1. There're 5 studies involving subjects of African descendents [7], [8], [10], [14], [15], 5 studies involving subjects of Caucasian descendents [9], [10], [12], [14], [16]. Four studies reported the effect of CCL3L1 CNV on HIV-1 susceptibility in mother-to-child transmission [7]–[10], 6 studies were about adults [10]–[12], [14]–[16].
In GCN ≤ PMN Vs. GCN > PMN model, the pooled OR was 1.35 (95% CI, 1.02–1.78, P = 0.000) (Figure 2a). Evaluation of publication bias by funnel plot (Figure 2b), Begg's test (P = 0.855) or Egger's test (P = 0.984) didn't reveal significant results.
Data of studies involving mixed race was set apart according to different ethnicity. AA, African American; EA, European American; HA, Hispanic American; OA, Other American except African American.
In GCN < PMN Vs. GCN ≥ PMN model, the pooled OR was 1.70 (95% CI, 1.30–2.23, P = 0.000) (Figure 3a). No asymmetry is observed in the funnel plot (Figure 3b), and neither Begg's test (P = 0.373) nor Egger's test (P = 0.324) suggested publication bias.
Data of studies involving mixed race was set apart according to different ethnicity.
Also, we performed stratified analyses by ethnicity, sample size and age group to explore potential sources of heterogeneity and detailed relationship between CCL3L1 CNV and susceptibility to HIV-1 infection. The results were summarized in Table 1. Most of the them were consistent with the main analyses which indicated that CCL3L1 CNV have distinct impact on susceptibility to HIV-1 infection and a lower copy number of CCL3L1 in specific population is associated with higher risk of HIV-1 infection. Besides, results from subgroups stratified by age suggests hat CCL3L1 may play different roles on the resistance to HIV-1 infection between infants and adults [10]. Since there was only one study performed in Japanese, Indians and Argentineans respectively, further studies on Asians and South Americans were needed. The funnel plots of stratified analyses didn't show asymmetry (figure not shown), but the results of Egger's test suggested that publication bias was evident in sub-infants studies of the GCN<PMN Vs. GCN≥PMN model (P = 0.027).
Sensitive analysis was conducted by deleting one study at a time to examine the influence of individual data-set to the pooled ORs. All of the corresponding pooled ORs were not materially altered (Figure S1, S2).
Discussion
Meta-analysis offers a powerful method to synthesize information of independent studies with similar target [33]. Considering a number of studies investigating CCL3L1 CNV and HIV-1 susceptibility have generated conflicting results, we performed this meta-analysis involving 9 eligible studies with 2434 cases and 4029 controls. The results suggested that CCL3L1 CNV is tightly linked to HIV-1 susceptibility. Individuals with lower copy number of CCL3L1 in the geographic ancestral population would be more susceptible to HIV-1 infection. The CCL3L-CCL4L region shows extensive architectural complexity, with smaller CNVs embedded within larger ones and with interindividual variation in breakpoints. Accounting for this genomic complexity is crucial for full interpretation of association studies, because the combinatorial content of CCL3L and CCL4L GCNs influences HIV/AIDS susceptibility. Methodological and epidemiological confounders and failure to account for the genomic complexity of the CCL3L-CCL4L locus underlie the lack of associations reported by several studies [34].
It is generally accepted that variations of gene copy number is a genetic determinant of phenotypic variation [6]. Since CCL3L1 encodes the natural ligand of CCR5 and increasing copy number of CCL3L1 down-regulates the expression of CCR5 on the cell surface [10], the HIV-1 entry-dependent effect of CCL3L1 on CCR5 used to be accepted as the major mechanism that inhibiting HIV-1 infection. Recent studies suggested that genotypes of CCL3L1-CCR5 influence cell-mediated immunity of individuals [35]. Individuals with higher copy number of CCL3L1 have greater CD4+ and CD8+ T cell response to HIV-1 gag protein [6], [29]. These findings indicated that both viral entry dependent effect and independent effect might explain the result of this meta-analysis.
Although the mechanism of CCL3L1 inhibiting HIV-1 infection has not been fully explored, outcomes of this meta-analysis confirmed that CCL3L1 CNV have distinct impact on HIV-1 susceptibility and a lower copy number of CCL3L1 in specific population is associated with higher risk of HIV-1 infection. Several factors might underlie the lack of observed association between CCL3L1 CNV and HIV-1 susceptibility. First, relatively small sample size would lead to results with too limited statistical power to detect possible relationship between genetic polymorphism and disease risk in genetic association studies [36]. Generally, large sample size is required for genetic association studies of single gene and disease susceptibility depending on the prevalence of the implicated polymorphism, since susceptibility of specific disease is always determined by numbers of genes [37]. Especially for people with relatively lower copy number of CCL3L1 like Caucasians, insufficient sample size would have generated a fluctuated risk estimate [38]. Second, selection of cases might have significant influence on the results. Infection with HIV-1 can exert a negative selective pressure on individuals with lower copy number of CCL3L1. Over time, the prevalence of cases with CCL3L1 copy number equal or greater than specific population median will increase because subjects with lower copy number of CCL3L1 progressed to AIDS or death more rapidly [10]. Thus, if selected cases weren't at an early stage of infection, similar distribution of CCL3L1 copy number would probably be observed in HIV-1 infected and uninfected subjects. Fourth, the susceptibility to HIV-1 infection is affected by a combination of genes besides CCL3L1. Nevertheless, few studies had dissected the combinatorial genomic complexity posed by varying proportions of distinct CCL3L and CCL4L genes among individuals [40]. Finally, Although most of the studies adopted similar real-time PCR method (Taqman assay) to measure the copy number of CCL3L1 in samples, minor methodological discrepancies of different studies as differences in DNA concentration and differences in primer and probe dye chemistry might have affected the results [39].
Some limitations of this meta-analysis should be acknowledged. First, publication bias was evident in subgroup of infants/hospital-based cases and hospital-based controls (P = 0.027) and subgroup of population-based cases and population-based controls (P = 0.014). The potential reason may be studies with advantage results would be accepted and published more easily. Thus, more studies are required for further analysis. Second, HIV-1 of R4 strain take advantage of CXCR4 as co-receptor but not CCR5. Therefore, virus entry-dependent effect of CCL3L1 won't affect HIV-1 infection of R4 strain. Nevertheless the newly discovered virus entry-independent effect might not be influenced despite HIV-1 virus type since most of the patients were infected by R5 strain. It is unlikely that virus of X4 strain would significantly affect the results. Third, in stratified analysis by ethnicity, the included studies regarded mostly Europeans and Africans. Only 300 subjects of Japanese and 511 subjects of Indians were included in published studies originated from Asia, which were too small to have enough statistical power. Additional studies are warranted to evaluate the association of CCL3L1 CNV and HIV-1 susceptibility in different ethnicities, especially in Asians. Forth, GCN estimates by currently quantitative PCR assays suffer from relatively low precision and accuracy with increasing gene copy number. In studies of Caucasians or other ethnicities that the median copy number of CCL3L1 is 2 or less, the methodological shortcomings should be a minor concern. But it might be more troublesome in studies of Africans with higher copy number [38]. Newer method with higher precision and accuracy will be helpful for a more exact estimate of the association between CCL3L1 CNV and HIV-1 susceptibility. Finally, controls of most studies were derived from healthy individuals. For studies concerning disease susceptibility, it'll be more proper to take samples from HIV-1-exposed seronegative (HES) individuals as controls. Considered the difficulty of obtaining samples from HES individuals, further studies of larger scale is required.
In conclusion, our meta-analysis involving 9 eligible studies with a total of more than 6000 subjects indicated significant association between CCL3L1 CNV and HIV-1 susceptibility. A lower copy number of CCL3L1 in the geographic ancestral population is associated with higher risk of HIV-1 infection. For further studies, it seems to be crucial to define precisely the genomic structure, taking into account the specific combination of the distinct genes within a CNV region [40], and considering (1) mechanism of CCL3L1 against HIV-1 infection; (2) discrepancies of methods on measuring CCL3L1 gene copy number; (3) CCL3L1's effect on Asians; (4) HES individuals as controls.
Supporting Information
Figure S1.
Sensitive test of the GCN≤PMN Vs. GCN>PMN model.
https://doi.org/10.1371/journal.pone.0015778.s001
(TIF)
Figure S2.
Sensitive test of the GCN<PMN Vs. CCL3L1 GCN≥PMN model.
https://doi.org/10.1371/journal.pone.0015778.s002
(TIF)
Table S1.
Characteristics of studies included in the meta-analysis.
https://doi.org/10.1371/journal.pone.0015778.s003
(DOC)
Acknowledgments
We gratefully acknowledge Prof. Jianming Tang at the University of Alabama for offering original data and assistance with manuscript preparation.
Author Contributions
Conceived and designed the experiments: HZZ. Performed the experiments: SJL. Analyzed the data: SJL. Contributed reagents/materials/analysis tools: SJL LY DLD. Wrote the paper: SJL LY.
References
- 1.
Epidemiology of AIDSDeath toll of AIDS has exceeded the first world war. Epidemiology of AIDSDeath toll of AIDS has exceeded the first world war.Available at: http://aids.39.net/ka/091/31/780270. Accessed 31 January 2009. Available at: http://aids.39.net/ka/091/31/780270. Accessed 31 January 2009.
- 2. Kaslow RA, Dorak T, Tang JJ (2005) Influence of host genetic variation on susceptibility to HIV type 1 infection. J Infect Dis 191: 568–572.RA KaslowT. DorakJJ Tang2005Influence of host genetic variation on susceptibility to HIV type 1 infection.J Infect Dis191568572
- 3. Telenti A, Goldstein DB (2006) Genomics meets HIV. Nat Rev Microbiol 4: 9–18.A. TelentiDB Goldstein2006Genomics meets HIV.Nat Rev Microbiol4918
- 4.
NCBI - Entrez GeneCCL3L1 chemokine (C-C motif) ligand 3-like 1. NCBI - Entrez GeneCCL3L1 chemokine (C-C motif) ligand 3-like 1.Available at: http://www.ncbi.nlm.nih.gov/gene/6349. Accessed 29 May 2010. Available at: http://www.ncbi.nlm.nih.gov/gene/6349. Accessed 29 May 2010.
- 5. Arenzana-Seisdedos F, Parmentier M (2006) Genetics of resistance to HIV infection: role of co-receptors and co-receptor ligands. Semin Immunol 18: 387–403.F. Arenzana-SeisdedosM. Parmentier2006Genetics of resistance to HIV infection: role of co-receptors and co-receptor ligands.Semin Immunol18387403
- 6. Nakajima T, Kaur G, Mehra N, Kimura A (2008) HIV/AIDS susceptibility and copy number variation in CCL3L1, a gene encoding a natural ligand for HIV-1 co-receptor CCR5. Cytogenet Genome Res 123: 156–160.T. NakajimaG. KaurN. MehraA. Kimura2008HIV/AIDS susceptibility and copy number variation in CCL3L1, a gene encoding a natural ligand for HIV-1 co-receptor CCR5.Cytogenet Genome Res123156160
- 7. Kuhn L, Schramm DB, Donninger S, Meddows-Taylor S, Coovadia AH, et al. (2007) African infants' CCL3 gene copies influence perinatal HIV transmission in the absence of maternal nevirapine. AIDS 21: 1753–1761.L. KuhnDB SchrammS. DonningerS. Meddows-TaylorAH Coovadia2007African infants' CCL3 gene copies influence perinatal HIV transmission in the absence of maternal nevirapine.AIDS2117531761
- 8. Meddows-Taylor S, Donninger SL, Paximadis M, Schramm DB, Anthony FS, et al. (2006) Reduced ability of newborns to produce CCL3 is associated with increased susceptibility to perinatal human immunodeficiency virus 1 transmission. J Gen Virol 87: 2055–2065.S. Meddows-TaylorSL DonningerM. PaximadisDB SchrammFS Anthony2006Reduced ability of newborns to produce CCL3 is associated with increased susceptibility to perinatal human immunodeficiency virus 1 transmission.J Gen Virol8720552065
- 9. Shostakovich-Koretskaya L, Catano G, Chykarenko ZA, He W, Gornalusse G, et al. (2009) Combinatorial content of CCL3L and CCL4L gene copy numbers influence HIV-AIDS susceptibility in Ukrainian children. AIDS 23: 679–688.L. Shostakovich-KoretskayaG. CatanoZA ChykarenkoW. HeG. Gornalusse2009Combinatorial content of CCL3L and CCL4L gene copy numbers influence HIV-AIDS susceptibility in Ukrainian children.AIDS23679688
- 10. Gonzalez E, Kulkarni H, Bolivar H, Mangano A, Sanchez R, et al. (2005) The influence of CCL3L1 gene-containing segmental duplications on HIV-1/AIDS susceptibility. Science 307: 1434–1440.E. GonzalezH. KulkarniH. BolivarA. ManganoR. Sanchez2005The influence of CCL3L1 gene-containing segmental duplications on HIV-1/AIDS susceptibility.Science30714341440
- 11. Nakajima T, Ohtani H, Naruse T, Shibata H, Mimaya JI, et al. (2007) Copy number variations of CCL3L1 and long-term prognosis of HIV-1 infection in asymptomatic HIV-infected Japanese with hemophilia. Immunogenetics 59: 793–798.T. NakajimaH. OhtaniT. NaruseH. ShibataJI Mimaya2007Copy number variations of CCL3L1 and long-term prognosis of HIV-1 infection in asymptomatic HIV-infected Japanese with hemophilia.Immunogenetics59793798
- 12. Huik K, Sadam M, Karki T, Avi R, Krispin T, et al. (2010) CCL3L1 Copy Number Is a Strong Genetic Determinant of HIV Seropositivity in Caucasian Intravenous Drug Users. JID 201: 730–739.K. HuikM. SadamT. KarkiR. AviT. Krispin2010CCL3L1 Copy Number Is a Strong Genetic Determinant of HIV Seropositivity in Caucasian Intravenous Drug Users.JID201730739
- 13. Urban TJ, Weintrob AC, Fellay J, Colombo S, Shianna KV, et al. (2009) CCL3L1 and HIV/AIDS susceptibility. Nat Med 15: 1009–1110.TJ UrbanAC WeintrobJ. FellayS. ColomboKV Shianna2009CCL3L1 and HIV/AIDS susceptibility.Nat Med1510091110
- 14. Bhattacharya T, Stanton J, Kim EY, Kunstman KJ, Phair JP, et al. (2009) CCL3L1 and HIV/AIDS susceptibility. Nat Med 15: 1112–1115.T. BhattacharyaJ. StantonEY KimKJ KunstmanJP Phair2009CCL3L1 and HIV/AIDS susceptibility.Nat Med1511121115
- 15. Shao W, Tang J, Song W, Wang C, Li Y, et al. (2007) CCL3L1 and CCL4L1: variable gene copy number in adolescents with and without human immunodeficiency virus type 1 (HIV-1) infection. Genes and Immunity 8: 224–231.W. ShaoJ. TangW. SongC. WangY. Li2007CCL3L1 and CCL4L1: variable gene copy number in adolescents with and without human immunodeficiency virus type 1 (HIV-1) infection.Genes and Immunity8224231
- 16. Rathore A, Chatterjee A, Sivarama P, Yamamoto N, Singhal PK, et al. (2009) Association of CCR5-59029 A/G and CCL3L1 Copy Number Polymorphism with HIV Type 1 Transmission/Progression among HIV Type 1-Seropositive and Repeatedly Sexually Exposed HIV Type 1-Seronegative North Indians. AIDS Research and Human Retroviruses 25: 1149–1156.A. RathoreA. ChatterjeeP. SivaramaN. YamamotoPK Singhal2009Association of CCR5-59029 A/G and CCL3L1 Copy Number Polymorphism with HIV Type 1 Transmission/Progression among HIV Type 1-Seropositive and Repeatedly Sexually Exposed HIV Type 1-Seronegative North Indians.AIDS Research and Human Retroviruses2511491156
- 17. Cochran W G (1954) The combination of estimates from different experiments. Biometrics: 10: 29.G. Cochran W1954The combination of estimates from different experiments.Biometrics:1029
- 18. Mantel N, Haenszel W (1959) Statistical aspects of the analysis of data from retrospective studies of disease. J Nat Cancer Inst 22: 719–748.N. MantelW. Haenszel1959Statistical aspects of the analysis of data from retrospective studies of disease.J Nat Cancer Inst22719748
- 19. Dersimonian R, Larid N (1986) Mata-analysis in clinical trials. Control Clin Trials 7: 177–188.R. DersimonianN. Larid1986Mata-analysis in clinical trials.Control Clin Trials7177188
- 20. Egger M, Davey Smith G, Schneider M, Minder C (1997) Bias in meta-analysis detected by a simple, graphical test. BMJ 315: 629–634.M. EggerG. Davey SmithM. SchneiderC. Minder1997Bias in meta-analysis detected by a simple, graphical test.BMJ315629634
- 21. Begg CB, Mazumdar M (1994) Operating characteristics of a rank correlation test for publication bias. Biometrics 50: 1088–1100.CB BeggM. Mazumdar1994Operating characteristics of a rank correlation test for publication bias.Biometrics5010881100
- 22. Tobias A (1999) Assessing the influence of a single study in the meta-analysis estimate. Stata Tech Bull 8: A. Tobias1999Assessing the influence of a single study in the meta-analysis estimate.Stata Tech Bull8
- 23. Bugeja MJ, Booth DR, Bennetts BH, Guerin J, Kaldor JM, et al. (2004) Analysis of the CCL3-L1 gene for association with HIV-1 susceptibility and disease progression. AIDS 18: 1069–1071.MJ BugejaDR BoothBH BennettsJ. GuerinJM Kaldor2004Analysis of the CCL3-L1 gene for association with HIV-1 susceptibility and disease progression.AIDS1810691071
- 24. Mackay CR (2005) CCL3L1 dose and HIV-1 susceptibility. TRENDS in Molecular Medicine; 11: 203–206.CR Mackay2005CCL3L1 dose and HIV-1 susceptibility.TRENDS in Molecular Medicine;11203206
- 25. Kulkarni H, Agan BK, Marconi VC, O'Connell RJ, Camargo JF, et al. (2008) CCL3L1-CCR5 Genotype Improves the Assessment of AIDS Risk in HIV-1-Infected Individuals. PLoS ONE 3: e3165.H. KulkarniBK AganVC MarconiRJ O'ConnellJF Camargo2008CCL3L1-CCR5 Genotype Improves the Assessment of AIDS Risk in HIV-1-Infected Individuals.PLoS ONE3e3165
- 26. Degenhardt JD, de Candia P, Chabot A, Schwartz S, Henderson L, et al. (2009) Copy Number Variation of CCL3-like Genes Affects Rate of Progression to Simian-AIDS in Rhesus Macaques (Macaca mulatta). PLoS Genetics 5: e1000346.JD DegenhardtP. de CandiaA. ChabotS. SchwartzL. Henderson2009Copy Number Variation of CCL3-like Genes Affects Rate of Progression to Simian-AIDS in Rhesus Macaques (Macaca mulatta).PLoS Genetics5e1000346
- 27. Gonzalez E, Dhanda R, Bamshad M, Mummidi S, Geevarghese R, et al. (2001) Global survey of genetic variation in CCR5, RANTES, and MIP-1a: Impact on the epidemiology of the HIV-1 pandemic. PNAS 98: 5199–5204.E. GonzalezR. DhandaM. BamshadS. MummidiR. Geevarghese2001Global survey of genetic variation in CCR5, RANTES, and MIP-1a: Impact on the epidemiology of the HIV-1 pandemic.PNAS9851995204
- 28. Moore JP, Klasse PJ (2007) HIV-1 Pathogenesis: The Complexities of the CCR5-CCL3L1 Complex. Cell Host & Microbe 2: 281–283.JP MoorePJ Klasse2007HIV-1 Pathogenesis: The Complexities of the CCR5-CCL3L1 Complex.Cell Host & Microbe2281283
- 29. Shalekoff S, Meddows-Taylor S, Schramm DB, Donninger SL, Gray GE, et al. (2008) Host CCL3L1 Gene Copy Number in Relation to HIV-1–Specific CD4+ and CD8+ T-Cell Responses and Viral Load in South African Women. J Acquir Immune Defic Syndr 48: 245–254.S. ShalekoffS. Meddows-TaylorDB SchrammSL DonningerGE Gray2008Host CCL3L1 Gene Copy Number in Relation to HIV-1–Specific CD4+ and CD8+ T-Cell Responses and Viral Load in South African Women.J Acquir Immune Defic Syndr48245254
- 30. Jülg B, Goebel FD (2005) Susceptibility to HIV/AIDS: An Individual Characteristic We Can Measure? Infection 33: 160–162.B. JülgFD Goebel2005Susceptibility to HIV/AIDS: An Individual Characteristic We Can Measure?Infection33160162
- 31. Modi WS, Lautenberger J, An P, Scott K, Goedert JJ, et al. (2006) Genetic Variation in the CCL18-CCL3-CCL4 Chemokine Gene Cluster Influences HIV Type 1 Transmission and AIDS Disease Progression. The American Journal of Human Genetics 79: 120–128.WS ModiJ. LautenbergerP. AnK. ScottJJ Goedert2006Genetic Variation in the CCL18-CCL3-CCL4 Chemokine Gene Cluster Influences HIV Type 1 Transmission and AIDS Disease Progression.The American Journal of Human Genetics79120128
- 32. Kaur G, Mehra N (2009) Genetic determinants of HIV-1 infection and progression to AIDS: susceptibility to HIV infection. John Wiley & Sons A/S-Tissue Antigens 73: 289–301.G. KaurN. Mehra2009Genetic determinants of HIV-1 infection and progression to AIDS: susceptibility to HIV infection.John Wiley & Sons A/S-Tissue Antigens73289301
- 33. Ioannidis JP, Rosenberg PS, Goedert JJ, O'Brien TR (2002) Meta-analysis of individual participants' data in genetic epidemiology. Am J Epidemiol 156: 204–210.JP IoannidisPS RosenbergJJ GoedertTR O'Brien2002Meta-analysis of individual participants' data in genetic epidemiology.Am J Epidemiol156204210
- 34. He W, Kulkarni H, Castiblanco J, Shimizu C, Aluyen U, et al. (2009) Reply to: “Experimental aspects of copy number variant assays at CCL3L1”. Nat Med 15: 1117–1120.W. HeH. KulkarniJ. CastiblancoC. ShimizuU. Aluyen2009Reply to: “Experimental aspects of copy number variant assays at CCL3L1”.Nat Med1511171120
- 35. Dolan MJ, Kulkarni H, Camargo JF, He W, Smith A, et al. (2007) CCL3L1 and CCR5 influence cell-mediated immunity and affect HIV-AIDS pathogenesis via viral entry-independent mechanisms. Nat Immunol 8: 1324–1336.MJ DolanH. KulkarniJF CamargoW. HeA. Smith2007CCL3L1 and CCR5 influence cell-mediated immunity and affect HIV-AIDS pathogenesis via viral entry-independent mechanisms.Nat Immunol813241336
- 36. Ioannidis JP (2002) Genetic associations: false or true? Trends Mol Med 2003 9: 135–138.JP Ioannidis2002Genetic associations: false or true?Trends Mol Med 20039135138
- 37. Hirschorn JN, Lohmueller K, Byrne E, Hirschorn K (2002) A comprehensive review of genetic association studies. Genet Med 4: 45–61.JN HirschornK. LohmuellerE. ByrneK. Hirschorn2002A comprehensive review of genetic association studies.Genet Med44561
- 38. Wacholder S, Chanok S, Garcia-Closas M, EI Ghormli L, Rothman N (2004) Accessing the probability that a positive report is false: an approach for molecular epidemiology studies. J Natl Cancer Inst 96: 434–442.S. WacholderS. ChanokM. Garcia-ClosasL. EI GhormliN. Rothman2004Accessing the probability that a positive report is false: an approach for molecular epidemiology studies.J Natl Cancer Inst96434442
- 39. Shrestha S, Tang J, Kaslow RA (2009) Gene copy number: learning to count past two. Nat Med 15: 1127–1129.S. ShresthaJ. TangRA Kaslow2009Gene copy number: learning to count past two.Nat Med1511271129
- 40. Colobran R, Pedrosa E, Carretero-lglesia L, Juan M (2010) Copy number variation in chemokine superfamily: the complex scene of CCL3L-CCL4L genes in health and disease. Clin Exp Immunol 162: 41–52.R. ColobranE. PedrosaL. Carretero-lglesiaM. Juan2010Copy number variation in chemokine superfamily: the complex scene of CCL3L-CCL4L genes in health and disease.Clin Exp Immunol1624152