Publications
bioRxiv : the preprint server for biologySep 2024 DOI:
10.1101/2024.09.07.611010

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

Mittl, Kristen; Hayashi, Fumie; Dandekar, Ravi; Schubert, Ryan D; 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; University of California, San Francisco MS-EPIC Team, ; Sibener, Leah; Cree, Bruce A C; Hauser, Stephen L; Hollenbach, Jill A; Gee, Marvin; Wilson, Michael R; Zamvil, Scott S; Sabatino, Joseph J
Product Used
Variant Libraries
Abstract
CD8+ 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.
Product Used
Variant Libraries

Related Publications