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Updated: May 23, 2026

Flow Cytometric Analysis of Lymphocyte Infiltration in Central Nervous System during Experimental Autoimmune Encephalomyelitis
Published on: November 17, 2020
Human endogenous retrovirus type W envelope expression in blood and brain cells provides new insights into multiple
Hervé Perron1, Raphaëlle Germi, Corinne Bernard
1GeNeuro, Geneva, Switzerland. hp@geneuro.com
Background:
The envelope protein from multiple sclerosis (MS) associated retroviral element (MSRV), a member of the Human Endogenous Retroviral family 'W' (HERV-W), induces dysimmunity and inflammation.
Objective:
The objective of this study was to confirm and specify the association between HERV-W/MSRV envelope (Env) expression and MS.
Methods:
103 MS, 199 healthy controls (HC) and controls with other neurological diseases (28), chronic infections (30) or autoimmunity (30) were analysed with an immunoassay detecting Env in serum. Env RNA or DNA copy numbers in peripheral blood mononuclear cells (PBMC) were determined by a quantitative polymerase chain reaction (PCR). Env was detected by immunohistology in the brains of patients with MS with three specific monoclonals.
Results:
Env antigen was detected in a serum of 73% of patients with MS with similar prevalence in all clinical forms, and not in chronic infection, systemic lupus, most other neurological diseases and healthy donors (p<0.01). Cases with chronic inflammatory demyelinating polyneuropathy (5/8) and rare HC (4/103) were positive. RNA expression in PBMC and DNA copy numbers were significantly elevated in patients with MS versus HC (p<0.001). In patients with MS, DNA copy numbers were significantly increased in chronic progressive MS (secondary progressive MS vs relapsing-remitting MS (RRMS) p<0.001; primary progressive MS vs RRMS -<0.02). Env protein was evidenced in macrophages within MS brain lesions with particular concentrations around vascular elements.
Conclusion:
The association between MS disease and the MSRV-type HERV-W element now appears quite strong, as evidenced ex-vivo from serum and PBMC with post-mortem confirmation in brain lesions. Chronic progressive MS, RRMS and clinically isolated syndrome show different ELISA (Enzyme-Linked Immunosorbent Assay) and/or PCR profiles suggestive of an increase with disease evolution, and amplicon sequencing confirms the association with particular HERV-W elements.
Insights
The Human Endogenous Retroviral family W (HERV-W) envelope protein is strongly associated with multiple sclerosis (MS). Elevated levels were found in MS patients' serum and peripheral blood mononuclear cells, confirming its link to the disease.
Area of Science:
- Neuroimmunology
- Retroviral Research
- Human Endogenous Retroviruses
Background:
- The envelope protein of the multiple sclerosis (MS) associated retroviral element (MSRV), a HERV-W family member, is implicated in immune dysfunction and inflammation.
- Understanding the role of HERV-W/MSRV in MS pathogenesis is crucial for developing targeted therapies.
Purpose of the Study:
- To confirm and specify the association between HERV-W/MSRV envelope (Env) expression and multiple sclerosis (MS).
- To investigate the prevalence and levels of HERV-W Env in MS patients compared to various control groups.
Main Methods:
- Immunoassay to detect Env in serum from 103 MS patients, 199 healthy controls (HC), and other disease cohorts.
- Quantitative PCR to determine Env RNA/DNA copy numbers in peripheral blood mononuclear cells (PBMC).
- Immunohistology to visualize Env in MS brain lesions.
Main Results:
- Env antigen detected in 73% of MS patients' serum, significantly higher than in controls (p<0.01).
- Significantly elevated Env RNA and DNA levels in MS patients' PBMC compared to HC (p<0.001).
- Increased DNA copy numbers correlated with disease progression in MS, with distinct profiles across clinical forms.
Conclusions:
- A strong association exists between MS and MSRV-type HERV-W, supported by ex-vivo and post-mortem brain lesion evidence.
- Distinct ELISA and PCR profiles suggest increasing HERV-W involvement with MS disease progression.
- Amplicon sequencing further confirms the specific association with particular HERV-W elements in MS.
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