Expanded T lymphocytes in the cerebrospinal fluid of multiple sclerosis patients are specific for Epstein-Barr-virus-infected B cells

• 成果类型: Article
• 署名作者: Gottlieb, Assaf; Pham, H. Phuong T.; Saltarrelli, Jerome G.; Lindsey, J. William
• 署名单位: University of Texas System; University of Texas Health Science Center Houston; University of Texas System; University of Texas Health Science Center Houston; University of Texas System; University of Texas Health Science Center Houston
• 刊物名称: PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
• ISSN/ISSBN: 0027-10739
• DOI: 10.1073/pnas.2315857121
• 发表日期: 2024-01-16
• 关键词: varicella-zoster-virus; disease-activity; immune-response; ebv; antibodies; enrichment; relapses; lesions

摘要

Epstein-Barr virus (EBV) infection has long been associated with multiple sclerosis (MS), but the role of EBV in the pathogenesis of MS is not clear. Our hypothesis is that a major fraction of the expanded clones of T lymphocytes in the cerebrospinal fluid (CSF) are specific for autologous EBV-infected B cells. We obtained blood and CSF samples from eight relapsing-remitting patients in the process of diagnosis. We stimulated cells from the blood with autologous EBV-infected lymphoblastoid cell lines (LCL), EBV, varicella zoster virus, influenza, and candida and sorted the responding cells with flow cytometry after 6 d. We sequenced the RNA for T cell receptors (TCR) from CSF, unselected blood cells, and the antigen-specific cells. We used the TCR V beta CDR3 sequences from the antigen-specific cells to assign antigen specificity to the sequences from the CSF and blood. LCL-specific cells comprised 13.0 +/- 4.3% (mean +/- SD) of the total reads present in CSF and 13.3 +/- 7.5% of the reads present in blood. The next most abundant antigen specificity was flu, which was 4.7 +/- 1.7% of the reads in the CSF and 9.3 +/- 6.6% in the blood. The prominence of LCL-specific reads was even more marked in the top 1% most abundant CSF clones with statistically significant 47% mean overlap with LCL. We conclude that LCL-specific sequences form a major portion of the TCR Tepertoire in both CSF and blood and that expanded clones specific for ECL are present-in MS CSF. This has important implications for the pathogenesis of MS.