The interaction between genetic and environmental factors is crucial to multiple sclerosis (MS) pathogenesis. Human Endogenous Retroviruses (HERVs) are endogenous viral elements of the human genome whose expression is associated with MS.
To perform a systematic review and meta-analysis and to assess qualitative and quantitative evidence on the expression of HERV families in MS patients.
Medline, Embase and the Cochrane Library were searched for published studies on the association of HERVs and MS. Meta-analysis was performed on the HERV-W family. Odds Ratio (OR) and 95% confidence interval (CI) were calculated for association.
43 reports were extracted (25 related to HERV-W, 13 to HERV-H, 9 to HERV-K, 5 to HRES-1 and 1 to HER-15 family). The analysis showed an association between expression of all HERV families and MS. For HERV-W, adequate data was available for meta-analysis. Results from meta-analyses of HERV-W were OR = 22.66 (95%CI 6.32 to 81.20) from 4 studies investigating MSRV/HERV-W (MS-associated retrovirus) envelope mRNA in peripheral blood mononuclear cells, OR = 44.11 (95%CI 12.95 to 150.30) from 6 studies of MSRV/HERV-W polymerase mRNA in serum/plasma and OR = 6.00 (95%CI 3.35 to 10.74) from 4 studies of MSRV/HERV-W polymerase mRNA in CSF.
Citation: Morandi E, Tanasescu R, Tarlinton RE, Constantinescu CS, Zhang W, Tench C, et al. (2017) The association between human endogenous retroviruses and multiple sclerosis: A systematic review and meta-analysis. PLoS ONE 12(2): e0172415. https://doi.org/10.1371/journal.pone.0172415
Editor: Klemens Ruprecht, Charite Universitatsmedizin Berlin, GERMANY
Received: October 2, 2016; Accepted: February 3, 2017; Published: February 16, 2017
Copyright: © 2017 Morandi 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.
Data Availability: All relevant data are within the paper and its Supporting Information files.
Funding: The authors received no specific funding for this work.
Competing interests: The authors have declared that no competing interests exist.
Multiple Sclerosis (MS) is a chronic demyelinating disease of the central nervous system (CNS) and one of the most common causes of neurological disability in young adults, with a higher incidence in women than men . Among environmental factors able to trigger MS pathogenesis on a background of genetic susceptibility, viral infections are of particular relevance. In addition to herpesviruses, such as HHV-6, VZV, and especially EBV , the expression of Human Endogenous Retrovirus (HERVs) has been considered as a risk factor for developing MS and for disease progression .
HERVs originate from exogenous infectious retroviruses that integrated into cells of the germ line 70 to 30 million years ago and came to represent almost 8% of the human genome. Over time, HERVs have generally lost their original capacity to retro-transpose or reinfect, having accumulated a series of mutations and recombination events. HERVs are multicopy families with each family consisting of many different loci in the human genome. They are classified into 31 families ranging in copy number from one to many thousands. These families are classified by a naming system on the basis of the tRNA specificity of the primer binding site, corresponding to the amino acid that would be added to the HERV were it translated into viral proteins (HERV-W,-K,-H etc.) . HERVs have generally maintained the same genetic structure as exogenous retroviruses. Two LTRs (Long Terminal Repeat) regions bound the genome with four major viral genes: gag (encoding matrix and retroviral core), pol (reverse transcriptase and integrase), pro (protease), and env (envelope) (Fig 1).
LTRs (Long Terminal Repeat) regions bound the genome with four major viral genes: gag (encoding matrix and retroviral core), pol (reverse transcriptase and integrase), pro (protease), and env (envelope).
The first HERV reported to be associated with MS in the late 1980s was the Multiple Sclerosis-associated retrovirus (MSRV), a member of the HERV-W family .
In addition to HERV-W, an increased expression of HERV-K and HERV-H families in the blood, brain or cerebrospinal fluid (CSF) from people with MS has also been reported by some groups , but not others .
The literature on this topic has been confused by a number of issues. The original studies on MSRV/HERV-W [5, 8] assumed that functional viral particles were involved and focussed on detection of cell-free (presumably virion associated) RNA. The later realisation that none of the 213 HERV-W loci in the human genome are fully replication competent cooled enthusiasm for the hypothesis of retroviral involvement in MS . Reports of an association between MSRV/HERV-W sequences and MS however continued, some affirming the association, some refuting it. Further confusion arose from these reports due to the plethora of detection methods (PCR and protein based), patient cohorts and sample types (blood, central nervous system, cell free and cell based) analysed (presented in this systematic review) and the variety of names given to the sequences detected. Recent detailed analysis of reported HERV-W/MSRV/Syncytin-1 sequences has demonstrated that they originate from a mosaic of loci and it is unlikely that the methods used to date are able to distinguish those from a single locus .
Subsequent to the initial reports of HERV association with MS, it has become clear that HERVs perform, at least in some cases, physiological roles in their hosts, with some HERV-W loci able to produce envelope proteins, in particular the syncytin-1 protein involved in human placental fusion . These proteins have also been demonstrated to have immunomodulatory effects in experimental models . It is also now clear that the promoter and enhancer elements in the proviral LTRs of endogenous retroviruses can and do act as transcriptional regulatory networks and affect the transcription levels of genes they are inserted in or near. In the case of HERV-W this is at least 55 genes, some previously associated with neurological disease .
The role of HERVs in MS both from an epidemiological association and a pathogenic mechanism point of view is therefore still a debateable topic. This systematic review therefore reviews the available data on the expression of different HERV families in MS patients and the methods used. In addition, we perform a meta-analysis of the expression of HERV-W env and pol RNA in MS patients and controls to resolve the epidemiological association of HERVs with MS
In performing this study, we followed the PRISMA (Preferred Reporting Items for Systematic reviews and Meta-Analyses) protocol . The PRISMA checklistis given in Supporting Information files (S1 Table). Details of the protocol for this systematic review were registered on PROSPERO (registration number CRD42016047290) and can be accessed at http://www.crd.york.ac.uk/PROSPERO/#index.php
Data source and search
Medline, Embase and the Cochrane Library up to 9th September 2016 were searched using the keywords “MULTIPLE SCLEROSIS” AND (“HERV” OR “HERVS” OR “HERV-W” OR “HERV-H” OR “HERV-K” OR “MSRV”) with no time restriction. Only papers published in English were included. Two independent investigators (EM and RTan) extracted the data from the literature databases and the references cited in the identified papers.
Full text articles were included in the systematic review if they were case-control studies containing data on the expression of viral proteins or RNA or DNA of any HERV family, in any type of tissue, from patients diagnosed with MS and from control groups (either healthy or pathological). Studies were further sub-grouped based on the retroviral family, the techniques employed, the protein/nucleic acid identified, and the type of tissue.
A subset of these articles was used for a quantitative meta-analysis if they studied the same protein or nucleic acid in the same type of tissue, using the same techniques. An additional inclusion criterion for the meta-analysis was the use of the same type of control group (healthy subjects or other controls). We performed a meta-analysis only if a minimum of 4 comparable studies met these criteria. Reviews and conference abstracts were excluded.
EM and RTan independently screened the papers yielded by the search to eliminate duplicates and to verify that inclusion criteria were met. Any disagreement was resolved through discussion with a third investigator (BG). The articles extracted were first organised in five different groups on the basis of the HERV families studied. From each eligible study the first author, the year of publication, the protein/nucleic acid investigated, the type of tissue analysed, the techniques used, the populations studied (number of cases and controls, number of women, mean age, source and type of disease), the country of origin, and a summary of the results were extracted independently by EM and RTan. Such results included the percentage or number of cases and controls considered positive for HERV expression, the presence or absence of an association and its statistical significance, as expressed by the authors, and any correlations with disease course, if available. The data extracted focused on the number of cases with HERV-W expression rather than the level of expression as too few studies reported quantitative expression levels for analysis.
The association of different viral proteins/nucleic acids with MS was analysed separately.
The odds ratio (OR) were estimated by the Mantel-Haenszel test and the standard error (SE) and the 95% confidence intervals (CI) were calculated using SPSS (IBM, version 22). We calculated the total OR, the p-value of fixed effects (inverse of variance) and of random effects (DerSimonian-Laird test) using StatsDirect (Version 2.8.0). We evaluated the heterogeneity calculating the Inconsistency (I2) and the Cochrane Q p-value. Egger’s regression test was used to examine publication bias.
The quality assessment of included studies was based on the Newcastle-Ottawa assessment scale (NOS) .
The online search identified 324 articles (Fig 2). After removing the duplicates, 244 articles were retained. A further 203 articles (58 reviews, 4 methodological papers, 136 articles that did not study the association between HERVs and MS, and 5 studies that were not case-control studies) were excluded. Forty-one papers were deemed eligible and 2 additional articles were identified from the references of the selected articles.
Articles identified and selected for the qualitative and quantitative synthesis.
The 43 papers included were categorised into 5 groups based on the HERV family studied (S2, S3, S4 and S5 Tables) and are presented in the Table 1. Six papers studied more than one HERV family and were included in more than one table. Twenty-five articles focused on HERV-W; 13 on HERV-H; 9 on HERV-K, whilst HRES-1 was studied in 5 and HERV-15 in 1 paper.
Examining all the publications found, we could perform three meta-analyses, in which at least 4 studies of association between HERV and MS reported the same viral targets, tissue samples and techniques compared to the same type of control group (either healthy or neurological controls). Four studies investigated RNA expression of the HERV-W sequence “MSRV/HERV-Wenv” by RT-PCR (Reverse transcriptase—polymerase chain reaction) in peripheral blood mononuclear cells (PBMC) from patients with MS and HC, 6 studies investigated RNA expression of the HERV-W sequence “MSRV/HERV-Wpol” detected by RT-PCR in the serum or plasma from MS patients and HC, and 4 studies investigated RNA expression of the HERV-W sequence “MSRV/HERV-Wpol” detected by RT-PCR in the CSF from MS patients and OND (Other Neurological Disease) controls. The remaining 25 studies were not included in the meta-analysis because they did not meet the inclusion criteria.
HERV-W in peripheral blood.
Expression of the MSRV/HERV-W viral proteins or RNA env and pol in the blood (PBMC or serum/plasma) was reported in 20 publications by Sardinian, French, Polish, Spanish, Brazilian, South African, Danish, German, and Canadian groups. In 15 studies MSRV/HERV-Wenv [10, 14–19] or MSRV/HERV-Wpol [5, 8, 17, 20–25] RNA or protein were found to be increased in serum/plasma or PBMC of MS patients compared to control groups (HC or OND) by different techniques [RT-PCR, Flow cytometry (FC) and ELISA].
Two studies demonstrated different levels of expression of the MSRV/HERV-Wenv in different types of blood cells [26, 27]. In these studies MSRV/HERV-Wenv RNA and protein expression detected by RT-PCR and FC were increased in monocytes, NK and B cells, but not in CD4+ and CD8+ T cells of MS patients compared to controls [26, 27]. Three studies (from Canada and Germany) did not detect increased levels of HERV-Wenv RNA (either MSRV/HERV-W or syncytin-1 that share 94% sequence identity at RNA level) in plasma, total PBMC and cell subtypes from MS patients compared to control groups [7, 28, 29].
HERV-W in the CSF.
Six papers studied the expression of HERV-W in the CSF from MS patients and controls. MSRV/HERV-Wpol and env RNA detected by RT-PCR were found to be over-expressed in people with MS compared with HC and OND by the French  and Italian groups [17, 20]. The Spanish  and Canadian groups [7, 28] did not find an increased expression of HERV-Wenv RNA by RT-PCR in MS patients.
HERV-W in the brain.
Nine publications studied the expression of MSRV/HERV-W in the brain tissue. A French and an Italian group showed the presence of MSRV/HERV-W Pol, Gag and Env proteins and RNA in infiltrating macrophages clustered around endothelial cells in MS lesions [18, 19, 31, 32], but not in the brain of HC or OND using immunohistochemistry and RT-PCR. By contrast, using the same techniques, a Canadian group found an increased expression of HERVWE1env RNA (syncytin-1) but not MSRV/HERV-Wenv, in the brains of MS patients compared to OND [7, 28, 33, 34]. A German group used Next Generation Sequencing (NGS) to detect the expression of HERV-W loci in the brain, without significant differences between HC and MS .
HERV-W in different types of MS.
Three studies in MS patients and HC looked at MSRV/HERV-W expression in different forms of MS. The French group found differences between Relapsing-remitting (RR-), primary-progressive (PP-) and secondary-progressive (SP-) MS with an increase of MSRV/HERV-Wenv DNA copy number, but not of RNA and protein expression, in the progressive forms of MS . The Spanish group detected a higher expression of MSRV/HERV-Wenv RNA in SPMS than RRMS . Patients with an elevated MSRV/HERV-Wenv DNA copy number had a higher degree of disability, according to their Expanded Disability Status Scale (EDSS) score .
For our meta-analysis of the association of MSRV/HERV-W with MS, 12 articles were suitable for inclusion according to the criteria described in the Methods. Together, these studies included 478 MS patients, 330 HC and 145 OND. The characteristics of participants in the included studies are summarised in Table 2. A separate meta-analysis was performed for each viral protein (env and pol) and for each different tissue. Four studies investigated MSRV/HERV-Wenv RNA in PBMC (111 MS patient and 58 HC), 6 studies investigated MSRV/HERV-Wpol RNA in serum/plasma (309 MS patients and 272 HC), and 4 studies investigated MSRV/HERV-Wpol RNA in CSF (187 MS patients and 145 HC).
Seventy of 111 MS patients (63%) and 10 of 58 HC (17.2%) expressed MSRV/HERV-Wenv in PBMC with an OR of 22.66 (95%CI 6.32–81.20; p<0.0001 for fixed and random effects, 0% inconsistency and Egger test for publication bias p = 0.22). Two-hundred forty-three of 309 MS patients (78.6%) and 41 of 272 HC (15%) expressed MSRV/HERV-Wpol in plasma/serum with an OR of 18.12 (95%CI 10.61–30.92; p<0.0001 for fixed effects) and OR of 44.11 (95%CI 12.95–150.30; p<0.0001 for random effect, inconsistency 61.2% and Egger test for publication bias p = 0.0088). One-hundred nine of 187 MS patients (58%) and 37 of 145 OND (25%) expressed MSRV/HERV-Wpol in CSF with an OR of 6.00 (95%CI 3.35–10.74; p<0.0001 for fixed and random effects, 0% inconsistency and Egger test for publication bias p = 0.55) (Fig 3).
Forest plot and bias assessment funnel plot of comparison of the expression of (A) MSRV/HERV-Wenv in PBMC, (B) MSRV/HERV-Wpol in serum/plasma, and (C) MSRV/HERV-Wpol in CSF in MS patients vs controls.
In the NOS scale of the quality assessment of the studies included in the meta-analysis the maximum score that could be achieved by a study was 10 stars. The majority of the studies scored less than half of the maximum score, with a mean of 4.5 (Table 3). The highest scoring study was Perron et al. 2012 with score of 8 stars . With regards to selection criteria, most studies had adequate definitions of cases and controls. The comparability of cases and controls was good for 6 studies that matched at least the age (Table 3). For the exposure criteria, all the studies used appropriate molecular techniques; 3 studies reported blinding sample analysts (Table 3). No studies reported a non-response rate (Table 3).
The presence of HERV-H in MS samples was detected for the first time by Christensen in 1998 . The expression of HERV-Henv and gag RNA by PCR was increased in the serum and PBMC of Danish MS [36, 37]. B cells and monocytes, but not T cells, from patients with active MS expressed higher levels of HERV-H Env protein detected by FC when compared to patients with stable MS and to controls .
In contrast, no difference in RNA expression was detected by CSF PCR between Spanish MS patients and neurological controls . Three studies did not find differences in the expression of HERV-Henv RNA in the brain  and PBMC  and HERV-Hgag RNA in the brain  between Canadian MS and OND patients.
The Danish group [38, 39] identified a SNP (single nucleotide polymorphisms) (rs391745) on HERV-Fc1 (a HERV-H retrovirus on chromosome X) that was associated with RRMS and SPMS in the Danish and Norwegian populations . They showed an increased expression of HERV-Fc1gag RNA in plasma and of HERV-Fc1Gag protein in T cells and monocytes in active MS patients compared to non-active MS and HC . The same group did not find differences in the HERV-Fc1gag DNA copy number in PBMC between the MS and HC groups .
A systematic review summarized the presence of HERV-Fc1 in the Spanish, Danish and Norwegian MS cohorts . The authors found an initial OR of 1.17 (p = 0.004; 95%CI: 1.05–1.30) in favour of the association which increased to 1.27 (95%CI: 1.11–1.45) after the Spanish cohort was excluded, bringing the heterogeneity from 82% to 0% .
Nine studies published by 6 different research groups in Denmark, France, Canada, UK, USA and Spain describe an association between MS and the HERV-K family (Table 1, S4 Table). More specifically, the studies focussed on the HERV-K10,-K115,-K113 and–K18 loci of this family. HERV K alleles (in particular the HERVK-113 and the HERV-K 115 loci) are known to be polymorphic in the human population (e.g., they are absent in some individuals)  which is an additional factor that may affect expression of these sequences in MS.
The first report in 1997 by a French group found no difference in the expression of HERV-K10env RNA in the PBMC and brain samples in MS patients compared to HC . The Canadian group reported an increased expression of HERV-Kpol , but not of HERV-Kenv [28, 33] in the brain of MS patients compared to control groups, using RT-qPCR. A British group used DNA PCR and showed an increased frequency of HERV-K113, but not HERV-K115, in MS and Sjogren`s syndrome compared to HC in a British population . The same authors could not reproduce the result in a larger study using unaffected parents of MS patients as control group , but a Danish group found an association between the SNP rs2435031 near HERV-K113 and MS .
A meta-analysis studying the link between HERV-K18 polymorphisms on chromosome 1 and autoimmune diseases found an association between the haplotype HERV-K18.3 (97Y-154W) and the American and Spanish MS population with an OR of 1.22 (95%CI:1.09–1.38) [48, 49]. A stronger association was detected in the subgroup of MS patients carrying the HLADRB1* 15:01 risk allele, known as a genetic risk factor for MS .
HRES and HERV-15
Rasmussen et al. in Denmark produced the 5 publications dealing with the relationship of the human T cell leukemia virus-related endogenous sequence (HRES) with MS (Table 1, S5 Table). These authors reported an association between MS and different haplotypes of HRES-1 defined on the basis of a SNP. They detected an increased frequency of haplotype 1 in British  and haplotypes 2 and 3 in Danish MS patients [51, 52], but no haplotype association in Chinese MS patients  compared to HC. There was no difference in the level of RNA expression of HRES-1 between Danish MS patients and HCs .
In this study we demonstrate an association between MS and HERVs.
The HERV-W family has been studied in most detail since the discovery of its member MSRV/HERV-W in biological samples obtained from MS patients . This is a multi-copy gene family, of which most loci are truncated or lack open reading frames. In the human genome there are at least 213 copies . We performed a qualitative and quantitative analysis of the available data on the association between HERV-W expression and MS. Overall, 20 of 25 articles that studied MSRV/HERV-W in MS report an association between MS and increased expression of MSRV/HERV-W in blood, CSF, and brain tissue. For the meta-analysis we had aimed at identifying retroviral family-specific articles that studied the presence or absence of the same protein or nucleic acid in the same type of tissue, using the same techniques. An additional inclusion criterion for the meta-analysis was the presence of the same control group. We decided to perform a meta-analysis only if a minimum of 4 studies met these criteria. On this basis, a quantitative meta-analysis could only be performed for a) HERV-W family MSRV/HERV-Wenv detected in PBMC of MS and HC by RT-PCR b) MSRV/HERV-Wpol detected in serum or plasma of MS and HC by RT-PCR and c) MSRV/HERV-Wpol detected in CSF of MS and OND by RT-PCR.
All the meta-analyses that we performed showed a strong association between MSRV/HERV-Wpol and MSRV/HERV-Wenv and MS.
Using healthy blood donors as control group, the results of the env meta-analysis showed a high OR (22.66) with no inconsistency or publication bias. High OR were obtained from the pol meta-analysis in serum/plasma as well, but a high heterogeneity between studies (61.2%) and evidence of publication bias were noted. Genetic differences between the studied populations could underlie such heterogeneity, at least in part. The study with the largest population in the pol meta-analysis was a multicentre study including patients from Sweden (32%), Spain (41%) and Sardinia (27%) , while the studies with very high OR, but a relatively small population, were only from Sardinia [20, 21], an Italian island with peculiar genetics and a high incidence of MS . Other important confounders could be sex, age and source of case and controls. Unfortunately due to limitations in the information provided by these articles (age, sex, type of MS, and source), it was not possible to stratify the population based on these parameters.
In line with the results found in the blood comparing MS and HC, the pol meta-analysis in CSF of MS and OND showed strong OR (6.00) as well, with no inconsistency or publication bias. This suggests that MSRV/HERV-Wpol expression is specifically associated with MS rather than general neurological diseases.
The major limitations of these meta-analyses are the relatively small population samples included in the analysis, which might not be representative of the whole population of patients with MS or controls, and the small number of studies included. The preponderance of papers from one Sardinian research group is a potential confounding factor in this meta-analysis, however the Sardinian cohort does not represent the majority of cases in each meta-analysis and all meta-analyses included studies from multiple groups and geographical locations with consistent results. There are regional genetic differences in MS prevalence with Sardinia having a very high incidence of the disease  and this may be reflected in the association of MS with HERV-W. However, it is clear that the association is found in more than just this one ethnic group. What is not clear despite the inclusion of one Brazilian cohort in the meta- analysis is whether this association holds true for all non-European populations.
Of all the articles studying HERV-W, only 4 were included in the meta-analysis for MSRV/HERV-Wenv in PBMC, 6 for MSRV/HERV-Wpol in serum/plasma and 4 for MSRV/HERV-Wpol in CSF. Only one of the publications with negative results was eligible for the quantitative analysis , while all the others did not meet the inclusion criteria, creating a potential bias. Specifically, Antony et al 2006  and 2007 , Schmitt et al 2013  and Laufer et al 2009  did not report data that could be interpreted as number of MSRV/HERV-W-positive and–negative MS and control subjects, but presented them as relative expression and often reporting only the mean or the p value for the differences. We decided not to establish arbitrary cut-off values to identify “positive” and “negative” samples because we cannot assume that every author would be able and willing to provide us with original data. On the other hand, positive/negative cut-off values are not explicitly presented in the publications included in the meta-analysis. For these reasons, we only used the data as they are actually presented in the peer-reviewed articles we have selected. Such papers were included in the qualitative, rather than quantitative analysis.
Among negative studies, Antony et al reported an association between MS and syncytin-1 rather than MSRV/HERV-Wenv. Syncytin-1 only describes the Env protein encoded by ERVWE-1, a replication-incompetent sequence on chromosome 7q21-22. At the RNA level the reported MSRV/HERV-Wenv sequence and syncytin-1 share 94% sequence identity, only differing for a 12-nucleotide insertion, making their discrimination difficult.
What is now clear is that the PCR-based methods used for detecting MSRV/HERV-W or Syncytin loci detect a mosaic of sequences rather than specific loci making such analysis difficult to interpret . Differences in real-time PCR methods  may also contribute to such complexity, which will require further clarification. PCR is the most commonly used method for HERV detection, but it does have limitations, including the inclusion or exclusion of different loci from the same group of viruses depending on the design of the primers used, which vary between studies (S6 Table). For the serum and PBMC studies included in the meta-analysis, we did not find a correlation between the primers used and the OR of the study. In the CSF, however, the only study that used a different set of primers reported the lowest OR (Alvarez Lafuente 2008 , S6 Table). This underlies the difficulty in establishing which HERV loci are responsible for differences observed between studies. Moreover, creation of recombinants between different sequences in vitro may also lead to detection of RNAs that do not originate from genomic DNA. It cannot be excluded that future improvements in detection techniques will lead to the discovery of additional HERVs associated with MS, but potentially also to disproving previously reported significant associations .
The issue of HERV-W complexity is also extended to studies of HERV protein expression. It often remains unclear as to which genomic locus the observed HERV proteins are derived from and therefore, whether the precise identity of the protein recognized by the MSRV/HERV-W Env antibodies can be established. A further set of potentially confounding factors are the reports of variation of DNA proviral copy number in the CNS tissue of MS and control patients [15, 19]. Given that HERV-W cannot function as a retrovirus capable of increasing its own copy number by de novo insertions there may be other factors involved, such as genetic variation in the presence or absence of certain HERV-W loci. This has not been previously reported for HERV-W, but does occur for other retroviral families such as HERV-K . It is also possible that other mechanisms of duplication of transposons (such as LINE retrotransposition) are at play.
The majority of the studies scored poorly (<5) in the NOS scale for quality assessment. This could be related to poor reporting rather than poor conduct (for example only 3 of 12 studies specified to use the same technique for cases and controls). Difficulties in the enrolment of community controls matched with at least two factors (age and sex) with MS patients could be a real bias to take in consideration in the analysis.
Overall, the association between MSRV/HERV-W and MS is strong. In addition to an association with a diagnosis of MS, the expression of MSRV/HERV-W has also been associated with the occurrence of disease progression.
From a mechanistic point of view, MSRV/HERV-W Env can activate Toll like receptor-4 (TLR4) and induce the production of iNOS and proinflammatory cytokines such as TNFα, IL-1β and IL-6, with associated reduction in oligodendrocyte differentiation capacity and myelin protein production [11, 58–60]. Furthermore, MSRV/HERV-W Env has immunostimulatory properties, as demonstrated by its capacity to substitute for mycobacterial lysate as a component of complete Freund’s adjuvant (CFA) in MOG35-55-induced EAE in C57-BL/6 mice, leading to full-blown disease . Such evidence suggests a possible role of MSRV/HERV-W in the pathogenesis of MS. It is possible, however, that the expression of MSRV/HERV-W in MS patients could be a consequence rather than a cause of inflammation, as suggested by increased expression of MSRV/HERV-W by monocytes stimulated by TNF-α .
The fact that herpesviruses can activate MSRV/HERV-W  suggests that EBV, an infectious environmental factor strongly associated with MS, could induce higher MSRV/HERV-W expression and underlie at least in part the association of HERVs with MS. Epigenetic regulation, escape from viral restriction factors, and other as yet unknown mechanisms could also explain this increased transcriptional activity in MS.
In addition to the HERV-W family, studies on HERV-H, HERV-K, HRES and HERV-15 also showed an association with MS in the qualitative analysis.
For these HERV families, 17 of 28 studies reported a significant association between HERV expression and MS, whereas the other 11 studies did not. More limited agreement between these studies may be explained by genetic differences among populations [52, 53], differences in the patterns of expression of different HERVs in CNS or peripheral tissues at different stages of MS , and by methodological issues. Technical issues were raised with regards to the adequate storage conditions of the samples  or the RT-PCR methodology used .
Unfortunately, for HERV families different from HERV-W, there are fewer than 4 studies meeting the mentioned inclusion criteria, therefore a quantitative analysis was not possible. With regards to HERV-Fc1 (H family, included in our qualitative analysis), a meta-analysis was already published by De la Hera et al 2014 , only focussing on the strength of association between the presence of the rs391745 SNP and MS.
In conclusion, our findings strongly support the evidence for an association between HERVs, and in particular MSRV/HERV-W, and MS. Further studies are required to better understand the nature and pathophysiology of this association.
S2 Table. Studies included in the HERV-W qualitative analysis: 25 articles studying the association between HERV-W and MS by 9 different research groups.
S3 Table. Studies included in the HERV-H qualitative analysis: 13 articles studying the association between HERV-H and MS by 3 different research groups.
S4 Table. Studies included in the HERV-K qualitative analysis: 9 articles studying the association between HERV-K and MS by 6 different research groups.
S5 Table. Studies included in the HRES and HERV-15 qualitative analysis: 5 articles studying the association between HRES and MS by 1 research group.
1 article studying the association between HERV-15 and MS by 1 research group.
- Conceptualization: EM RT RET CSC WZ CT BG.
- Formal analysis: EM WZ CT.
- Funding acquisition: BG.
- Investigation: EM RT.
- Methodology: EM RT RET CSC WZ CT BG.
- Project administration: EM BG.
- Resources: WZ CT.
- Software: WZ CT.
- Supervision: RT RET BG.
- Validation: EM RT BG.
- Visualization: EM WZ BG.
- Writing – original draft: EM.
- Writing – review & editing: EM RT RET CSC WZ CT BG.
- 1. Bar-Or A. Multiple Sclerosis and related disorderes: evolving pathophysiologic insights. Lancet Neurol. 2016; 15(1):9–11. pmid:26700897
- 2. Ascherio A, Munger KL. Environmental risk factors for multiple sclerosis. Part I: the role of infection. Ann Neurol. 2007; 61(4):288–99. pmid:17444504
- 3. Perron H, Bernard C, Bertrand JB, Lang AB, Popa I, Sanhadji K, et al. Endogenous retroviral genes, herpesviruses and gender in Multiple Sclerosis. J Neurol Sci. 2009; 286(1–2):65–72. pmid:19447411
- 4. Gifford R, Tristem M. The evolution, distribution and diversity of endogenous retroviruses. Virus genes. 2003; 26:291–315. pmid:12876457
- 5. Perron H, Garson JA, Bedin F, Beseme F, Paranhos-Baccala G, Komurian-Pradel F, et al. Molecular identification of a novel retrovirus repeatedly isolated from patients with multiple sclerosis. Proc Natl Acad Sci. 1997; 94:7583–8. pmid:9207135
- 6. Christensen T. Association of human endogenous retroviruses with multiple sclerosis and possible interactions with herpes viruses. Rev Med Virol. 2005; 15(3):179–211. pmid:15782388
- 7. Antony JM, Zhu Y, Izad M, Warren KG, Vodjgani M, Mallet F, et al. Comparative expression of human endogenous retrovirus-W genes in multiple sclerosis. AIDS Res Hum Retroviruses. 2007; 23(10):1251–6. pmid:17961112
- 8. Garson JA, Tuke PW, Giraud P, Paranhos-Baccala G, Perron H. Detection of virion-associated MSRV-RNA in serum of patients with multiple sclerosis. Lancet. 1998; 351(9095):33. pmid:9433428
- 9. Grandi N, Cadeddu M, Blomberg J, Tramontano E. Contribution of type W human endogenous retroviruses to the human genome: characterization of HERV-W proviral insertions and processed pseudogenes. Retrovirology. 2016;13(1):67. pmid:27613107
- 10. Mameli G, Poddighe L, Astone V, Delogu G, Arru G, Sotgiu S, et al. Novel reliable real-time PCR for differential detection of MSRVenv and syncytin-1 in RNA and DNA from patients with multiple sclerosis. J Virol Methods. 2009; 161(1):98–106. pmid:19505508
- 11. Perron H, Dougier-Reynaud HL, Lomparski C, Popa I, Firouzi R, Bertrand JB, et al. Human endogenous retrovirus protein activates innate immunity and promotes experimental allergic encephalomyelitis in mice. PloS One. 2013; 8(12):e80128. pmid:24324591
- 12. Moher D, Liberati A, Tetzlaff J, Altman DG, The PRISMA Group. Preferred reporting Items for systematic reviews and meta-analyses: The PRISMA Statement. PloS Med. 2009; 6:e1000100.
- 13. Wells GA, Shea B, O'Connell D, Peterson J, Welch V, Losos M, et al. The Newcastle-Ottawa Scale (NOS) for assessing the quality of nonrandomised studies in meta-analyses. 2012; http://www.ohri.ca/programs/clinical_epidemiology/oxford.asp
- 14. Garcia-Montojo M, de la Hera B, Varade J, de la Encarnacion A, Camacho I,Dominguez-Mozo M, et al. HERV-W polymorphism in chromosome X is associated with multiple sclerosis risk and with differential expression of MSRV. Retrovirology. 2014; 11:2. pmid:24405691
- 15. Garcia-Montojo M, Dominguez-Mozo M, Arias-Leal A, Garcia-Martinez A, de las Heras V, Casanova I et al. The DNA copy number of human endogenous retrovirus-W (MSRV-Type) is increased in multiple scleorosis patients and is influenced by gender and disease severity. PloS One. 2013; 8:e53623. pmid:23308264
- 16. do Olival GS, Faria TS, Nali LH, de Oliveira AC, Casseb J, Vidal JE, et al. Genomic analysis of ERVWE2 locus in patients with multiple sclerosis: absence of genetic association but potential role of human endogenous retrovirus type W elements in molecular mimicry with myelin antigen. Front Microbiol. 2013; 4:172. pmid:23805135
- 17. Arru G, Mameli G, Astone V, Serra C, Huang Y, Link H et al. Multiple sclerosis and HERV-W/MSRV: a multicentric study. Int J Biomed Sci. 2007; 3:292–7. pmid:23675056
- 18. Mameli G, Astone V, Arru G, Marconi S, Lovato L, Serra C, et al. Brains and peripheral blood mononuclear cells of multiple sclerosis (MS) patients hyperexpress MS-associated retrovirus/HERV-W endogenous retrovirus, but not Human herpesvirus 6. J Gen Virol. 2007; 88(Pt 1):264–74. pmid:17170460
- 19. Perron H, Germi R, Bernard C, Garcia-Montojo M, Deluen C, Farinelli L, et al. Human endogenous retrovirus type W envelope expression in blood and brain cells provides new insights into multiple sclerosis disease. Mult Scler. 2012; 18(12):1721–36. pmid:22457345
- 20. Dolei A, Serra C, Mameli G, Pugliatti M, Sechi G, Cirotto MC, et al. Multiple sclerosis-associated retrovirus (MSRV) in Sardinian MS patients. Neurology. 2002;58(3):471–3. pmid:11839854
- 21. Serra C, Sotgiu S, Mameli G, Pugliatti M, Rosati G, Dolei A. Multiple sclerosis and multiple sclerosis-associated retrovirus in Sardinia. Nuerol Sci. 2001; 22:171–3.
- 22. Ménard A, Amouri R, Michel M, Marcel F, Brouillet A, Belliveau J, et al. Gliotoxicity, reverse transcriptase activity and retroviral RNA in monocyte/macrophage culture supernatants from patients with multiple sclerosis. FEBS letters. 1997; 413(3):477–85. pmid:9303559
- 23. de Villiers JN, Treurnicht FK, Warnich L, Carr J, van Rensburg SJ, Kotze MJ. Analysis of viral and genetic factors in South African patients with multiple sclerosis. Metab Brain Dis. 2006; 21(2–3):163–9. pmid:16865539
- 24. Zawada M, Liwen I, Pernak M, Januszkiewicz-Lewandowska D, Nowicka-Kujawska K, Rembowska J, et al. MSRV POL sequence copy number as potential marker of multiple sclerosis. Pol J Pharmacol. 2003; 55:869–75. pmid:14704480
- 25. Nowak J, Januszkiewicz D, Pernak M, Liwen I, Zawada M, Rembowska J, et al. Multiple sclerosis-associated virus-related pol sequences found both in multiple sclerosis and healthy donors are more frequently expressed in multiple sclerosis patients. J Neurovirol. 2003; 9(1):112–7. pmid:12587074
- 26. Brudek T, Christensen T, Aagaard L, Petersen T, Hansen HJ, Moller-Larsen A. B cells and monocytes from patients with active multiple sclerosis exhibit increased surface expression of both HERV-H Env and HERV-W Env, accompanied by increased seroreactivity. Retrovirology. 2009; 6:104. pmid:19917105
- 27. Mameli G, Poddighe L, Mei A, Uleri E, Sotgiu S, Serra C, et al. Expression and activation by Epstein Barr virus of human endogenous retroviruses-W in blood cells and astrocytes: inference for multiple sclerosis. PloS One. 2012; 7(9):e44991. pmid:23028727
- 28. Antony JM, Izad M, Bar-Or A, Warren KG, Vodjgani M, Mallet F, et al. Quantitative analysis of human endogenous retrovirus-Wenv in neuroinflammatory diseases. Aids Res Hum Retroviruses. 2006;22:1253–9. pmid:17209768
- 29. Laufer G, Mayer J, Mueller BF, Mueller-Lantzsch N, Ruprecht K. Analysis of transcribed human endogenous retrovirus W env loci clarifies the origin of multiple sclerosis-associated retrovirus env sequences. Retrovirology. 2009; 6:37. pmid:19368703
- 30. Alvarez-Lafuente R, Garcia-Montojo M, De Las Heras V, Dominguez-Mozo MI, Bartolome M, Benito-Martin MS, et al. Herpesviruses and human endogenous retroviral sequences in the cerebrospinal fluid of multiple sclerosis patients. Mult Scler. 2008; 14(5):595–601. pmid:18566025
- 31. Perron H, Lazarini F, Ruprecht K, Pechoux-Longin C, Seilhean D, Sazdovitch V, et al. Human endogenous retrovirus (HERV)-W ENV and GAG proteins: physiological expression in human brain and pathophysiological modulation in multiple sclerosis lesions. J Neurovirol. 2005; 11(1):23–33. pmid:15804956
- 32. van Horssen J, van der Pol S, Nijland P, Amor S, Perron H. Human endogenous retrovirus W in brain lesions: Rationale for targeted therapy in multiple sclerosis. Mult Scler Relat Disord. 2016; 8:11–8. pmid:27456869
- 33. Antony JM, van Marle G, Opii W, Butterfield DA, Mallet F, Yong VW, et al. Human endogenous retrovirus glycoprotein-mediated induction of redox reactants causes oligodendrocyte death and demyelination. Nat Neurosci. 2004; 7(10):1088–95. pmid:15452578
- 34. Johnston JB, Silva C, Holden J, Warren KG, Clark AW, Power C. Monocyte activation and differentiation augment human endogenous retrovirus expression: Implications for inflammatory brain diseases. Ann Neurol. 2001; 50(4):434–42. pmid:11601494
- 35. Schmitt K, Richter C, Backes C, Meese E, Ruprecht K, Mayer J. Comprehensive analysis of human endogenous retrovirus group HERV-W locus transcription in multiple sclerosis brain lesions by high-throughput amplicon sequencing. J Virol. 2013; 87(24):13837–52. pmid:24109235
- 36. Christensen T, Sørensen PD, Riemann H, Hansen HJ, Munch M, Haaher S, et al. Molecular characterization of HERV-H variants associated with multiple sclerosis. Acta Neurol Scand. 2000; 101:229–38. pmid:10770518
- 37. Christensen T, Sørensen PD, Hansen HJ, Møller-Larsen A. Antibodies against a human endogenous retrovirus and the preponderance of env splice variants in multiple sclerosis patients. Mult Scler. 2003; 9(1):6–15. pmid:12617261
- 38. Nexø BA, Christensen T, Frederiksen J, Møller-Larsen A, Oturai AB, Villesen P, et al. The etiology of multiple sclerosis: genetic evidence for the involvement of the human endogenous retrovirus HERV-Fc1. PloS One. 2011; 6:e16652. pmid:21311761
- 39. Nexø BA, Villesen P, Nissen KK, Lindegaard HM, Rossing P, Petersen T, et al. Are human endogenous retroviruses triggers of autoimmune diseases? Unveiling associations of three diseases and viral loci. Immunol Res. 2016; 64(1):55–63. pmid:26091722
- 40. Hansen B, Oturai AB, Harbo HF, Celius EG, Nissen KK, Laska MJ, et al. Genetic association of multiple sclerosis with the marker rs391745 near the endogenous retroviral locus HERV- Fc1: analysis of disease subtypes. PloS One. 2011;
- 41. Laska MJ, Brudek T, Nissen KK, Christensen T, Moller-Larsen A, Petersen T, et al. Expression of HERV-Fc1, a human endogenous retrovirus, is increased in patients with active multiple sclerosis. J Virol. 2012; 86(7):3713–22. pmid:22278236
- 42. Nissen KK, Laska MJ, Hansen B, Pedersen FS, Nexo BA. No additional copies of HERV-Fc1 in the germ line of multiple sclerosis patients. J Virol. 2012; 9:188.
- 43. de la Hera B, Varade J, Garcia-Montojo M, Alcina A, Fedetz M, Alloza I, et al. Human endogenous retrovirus HERV-Fc1 association with multiple sclerosis susceptibility: a meta-analysis. PloS One. 2014; 9(3):e90182. pmid:24594754
- 44. Wildschutte JH, Williams ZH, Montesionb M, Subramanianb RP, Jidd JM, Coffin JM. Discovery of unfixed endogenous retrovirus insertions in diverse human populations. Proc Natl Acad Sci U S A. 2016; 113(16):E2326–34. pmid:27001843
- 45. Rasmussen HB, Geny C, Deforges L, Perron H, Tourtelotte W, Heltberg A, et al. Expression of endogenous retroviruses in blood mononuclear cells and brain tissue from multiple sclerosis patients. Acta Neurol Scand. 1997; 169:38–44.
- 46. Moyes DL, Martin A, Sawcer S, Temperton N, Worthington J, Griffiths DJ, et al. The distribution of the endogenous retroviruses HERV-K113 and HERV-K115 in health and disease. Genomics. 2005; 86(3):337–41. pmid:16024218
- 47. Moyes DL, Goris A, Ban M, Compston A, Griffiths DJ, Sawcer S, et al. HERV-K113 is not associated with multiple sclerosis in a large family-based study. AIDS Res Hum Retroviruses. 2008; 24(3):363–5. pmid:18327982
- 48. de la Hera B, Varade J, Garcia-Montojo M, Lamas JR, de la Encarnacion A, Arroyo R, et al. Role of the human endogenous retrovirus HERV-K18 in autoimmune disease susceptibility: study in the Spanish population and meta-analysis. PloS One. 2013; 8(4):e62090. pmid:23634223
- 49. Tai AK, O'Reilly EJ, Alroy KA, Simon KC, Munger KL, Huber BT, et al. Human endogenous retrovirus-K18 Env as a risk factor in multiple sclerosis. Mult Scler. 2008; 14(9):1175–80. pmid:18701576
- 50. Rasmussen HB, Kelly MA, Francis DA, Clausen J. Association between the endogenous retrovirus HRES-1 and multiple sclerosis in the United Kingdom—evidence of genetically different disease subsets? Dis Markers. 2000; 16:101–4. pmid:11381188
- 51. Rasmussen HB, Clausen J. A Novel Haplotype of the Endogenous Retrovirus, HRES-1, in Patients with Multiple Sclerosis and Healthy Individuals. Autoimmunity. 1999;29:141–5. pmid:10433076
- 52. Rasmussen HB, Heltberg A, Christensen K, Clausen J. Possible association between multiple sclerosis and the human T cell leukemia virus (HTLV)-reloted endogenous element, HRES- I. Mult Scler. 1996; 2:133–6. pmid:9345377
- 53. Rasmussen HB, Kelly MA, Francis DA, Clausen J. Haplotypes of the endogenous retrovirus HRES-i in multiple sclerosis patients and healthy control subjects of shanghai chinese origin. Dis Markers. 1998; 13:251–5. pmid:9553740
- 54. Martinelli-Boneschi F, Esposito F, Brambilla P, Lindstrom E, Lavorgna G, Stankovich J, et al. A genome-wide association study in progressive multiple sclerosis. Mult Scler. 2012; 18(10):1384–94. pmid:22457343
- 55. Sotgiu S, Pugliatti M, Sanna A, Sotgiu A, Castiglia P, Solinas G et al. Multiple sclerosis complexity in selected populations: the challenge of Sardinia, insular Italy. Eur J Neurol. 2002; 9:329–41. pmid:12099914
- 56. Pugliatti M, Sotgiu S, Solinas G, Castiglia P, Pirastru MI, Murgia B, et al. Multiple Sclerosis epidemiology in Sardinia: evidence for a true increasing risk. Acta Neurol Scand. 2001; 103(1):20–6. pmid:11153884
- 57. Garson JA, Huggett JF, Bustin SA, Pfaffl MW, Benes V, Vandesompele J, et al. Unreliable real-time PCR analysis of human endogenous retrovirus-W (HERV-W) RNA expression and DNA copy number in multiple sclerosis. AIDS Res Hum Retroviruses. 2009; 25:377–8. pmid:19292592
- 58. Rolland A, Jouvin-Marche E, Viret C, Faure M, Perron H, Marche P. The envelope protein of a human endogenous retrovirus-W family activates innate immunity through CD14/TLR4 and promotes Th1-like responses. J Immunol. 2006; 176:7636–44. pmid:16751411
- 59. Kremer D, Schichel T, Forster M, Tzekova N, Bernard C, van der Valk P, et al. Human endogenous retrovirus type W envelope protein inhibits oligodendroglial precursor cell differentiation. Ann Neurol. 2013;74(5):721–32. pmid:23836485
- 60. Duperray A, Barbe D, Raguenez G, Weksler BB, Romero IA, Couraud PO, et al. Inflammatory response of endothelial cells to a human endogenous retrovirus associated with multiple sclerosis is mediated by TLR4. Int Immunol. 2015;27(11):545–53. pmid:25957268