Antigen-specificity of clonally-enriched CD8+ T cells in multiple sclerosis

Author:

Mittl Kristen,Hayashi Fumie,Dandekar Ravi,Schubert Ryan D.ORCID,Gerdts Josiah,Oshiro Lindsay,Loudermilk Rita,Greenfield Ariele,Augusto Danillo G.,Ramesh Akshaya,Tran Edwina,Koshal Kaniskha,Kizer Kerry,Dreux Joanna,Cagalingan Alaina,Schustek Florian,Flood Lena,Moore Tamson,Kirkemo Lisa L.,Cooper Tiffany,Harms Meagan,Gomez Refujia, , ,Sibener Leah,Cree Bruce A. C.,Hauser Stephen L.,Hollenbach Jill A.,Gee Marvin,Wilson Michael R.ORCID,Zamvil Scott S.,Sabatino Joseph J.ORCID

Abstract

AbstractCD8+ T cells are the dominant lymphocyte population in multiple sclerosis (MS) lesions where they are highly clonally expanded. The clonal identity, function, and antigen specificity of CD8+ T cells in MS are not well understood. Here we report a comprehensive single-cell RNA-seq and T cell receptor (TCR)-seq analysis of the cerebrospinal fluid (CSF) and blood from a cohort of treatment-naïve MS patients and control participants. A small subset of highly expanded and activated CSF-enriched CD8+ T cells were abundant in people with MS and displayed high cytotoxicity and tissue-homing transcriptional profiles. Using a combination of unbiased and targeted antigen discovery approaches, several MS-derived CD8+ T cell clonotypes recognizing Epstein-Barr virus (EBV) antigens and novel mimotopes were identified. These findings shed insight into the functions of CD8+ T cells in MS and may serve as potential disease biomarkers and therapeutic targets.Abstract FigureGraphical SummaryCreated in BioRender. Sabatino, J. (2024)BioRender.com/e66l598

Publisher

Cold Spring Harbor Laboratory

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