Broader Epstein–Barr virus–specific T cell receptor repertoire in patients with multiple sclerosis

Tilman Schneider‐Hohendorf(University of Münster), Lisa Ann Gerdes(Munich Cluster for Systems Neurology), Béatrice Pignolet(Université Toulouse III - Paul Sabatier), Rachel M. Gittelman(Adaptive Biotechnologies (United States)), Patrick Ostkamp(University of Münster), Florian Rubelt(La Roche College), Catarina Raposo(Roche (Switzerland)), Björn Tackenberg(Roche (Switzerland)), Marianne Riepenhausen(University of Münster), Claudia Janoschka(University of Münster), Christian Wünsch(University of Münster), Florence Bucciarelli(Université Toulouse III - Paul Sabatier), Andrea Flierl‐Hecht(Munich Cluster for Systems Neurology), Eduardo Beltrán(Munich Cluster for Systems Neurology), Tania Kümpfel(Munich Cluster for Systems Neurology), Katja Anslinger(Ludwig-Maximilians-Universität München), Catharina C. Groß(University of Münster), Heidi Chapman(Adaptive Biotechnologies (United States)), Ian M. Kaplan(Adaptive Biotechnologies (United States)), David Brassat(Roche (Switzerland)), Hartmut Wekerle(Ludwig-Maximilians-Universität München), Martin Kerschensteiner(Munich Cluster for Systems Neurology), Luisa Klotz(University of Münster), Jan D. Lünemann(University of Münster), Reinhard Hohlfeld(Ludwig-Maximilians-Universität München), Roland Liblau(Université Toulouse III - Paul Sabatier), Heinz Wiendl(University of Münster), Nicholas Schwab(University of Münster)
The Journal of Experimental Medicine
September 1, 2022
Cited by 85Open Access
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Abstract

Epstein-Barr virus (EBV) infection precedes multiple sclerosis (MS) pathology and cross-reactive antibodies might link EBV infection to CNS autoimmunity. As an altered anti-EBV T cell reaction was suggested in MS, we queried peripheral blood T cell receptor β chain (TCRβ) repertoires of 1,395 MS patients, 887 controls, and 35 monozygotic, MS-discordant twin pairs for multimer-confirmed, viral antigen-specific TCRβ sequences. We detected more MHC-I-restricted EBV-specific TCRβ sequences in MS patients. Differences in genetics or upbringing could be excluded by validation in monozygotic twin pairs discordant for MS. Anti-VLA-4 treatment amplified this observation, while interferon β- or anti-CD20 treatment did not modulate EBV-specific T cell occurrence. In healthy individuals, EBV-specific CD8+ T cells were of an effector-memory phenotype in peripheral blood and cerebrospinal fluid. In MS patients, cerebrospinal fluid also contained EBV-specific central-memory CD8+ T cells, suggesting recent priming. Therefore, MS is not only preceded by EBV infection, but also associated with broader EBV-specific TCR repertoires, consistent with an ongoing anti-EBV immune reaction in MS.


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