Persistent and compartmentalized T cell immunity in ALS

Abstract Amyotrophic lateral sclerosis is a fatal neurodegenerative disease increasingly linked to T cell responses, although the mechanisms driving T cell activation and disease progression remain unclear. Here we used single-cell RNA and T cell receptor sequencing, longitudinal immune profiling and imaging flow cytometry to identify long-lived intrathecal clonotypes and antigen-presenting cell–T cell complexes displaying features of immunological synapse formation, consistent with intrathecal antigen presentation. Higher frequencies of CD4 + effector, CD4 + regulatory and CD8 + T cells in cerebrospinal fluid (CSF) were associated with slower disease progression, whereas increased circulating CD4 + effector and regulatory T cells were associated with faster progression. T cell clonotypes shared between blood and CSF exhibited distinct transcriptional states. Finally, frequencies of cytomegalovirus-specific T cells in CSF and anticytomegalovirus serum antibodies were correlated with faster progression and shorter survival in sporadic amyotrophic lateral sclerosis. These findings reveal compartmentalized immune dynamics, largely contrasting protective intrathecal responses with harmful systemic activation.

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Publication Details

Journal
Nature Medicine
Published
2026-10-27
DOI
https://doi.org/10.1038/s41591-026-04728-5
Primary Topic
Amyotrophic Lateral Sclerosis Research
Type
article
Field-Weighted Citation Impact
0.00

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article

Persistent and compartmentalized T cell immunity in ALS

John Andersson, Hans Grönlund, Elie Deeba, Joonas Lehikoinen et al.
1 links
Nature Medicine
Amyotrophic Lateral Sclerosis Research
article

Persistent and compartmentalized T cell immunity in ALS

John Andersson, Hans Grönlund, Elie Deeba, Joonas Lehikoinen, Solmaz Yazdani, Christina Seitz, Márton Keszei, Anikó Lovik, Caroline Ingre, Pentti J. Tienari, Hannu Laaksovirta, 陈振振, Fang Fang, Jannika Mansikkaviita
article en

Abstract

Abstract Amyotrophic lateral sclerosis is a fatal neurodegenerative disease increasingly linked to T cell responses, although the mechanisms driving T cell activation and disease progression remain unclear. Here we used single-cell RNA and T cell receptor sequencing, longitudinal immune profiling and imaging flow cytometry to identify long-lived intrathecal clonotypes and antigen-presenting cell–T cell complexes displaying features of immunological synapse formation, consistent with intrathecal antigen presentation. Higher frequencies of CD4 + effector, CD4 + regulatory and CD8 + T cells in cerebrospinal fluid (CSF) were associated with slower disease progression, whereas increased circulating CD4 + effector and regulatory T cells were associated with faster progression. T cell clonotypes shared between blood and CSF exhibited distinct transcriptional states. Finally, frequencies of cytomegalovirus-specific T cells in CSF and anticytomegalovirus serum antibodies were correlated with faster progression and shorter survival in sporadic amyotrophic lateral sclerosis. These findings reveal compartmentalized immune dynamics, largely contrasting protective intrathecal responses with harmful systemic activation.

Nature Medicine
Leiden University (NL), Public Health Agency of Sweden (SE), Karolinska University Hospital (SE), University of Helsinki (FI), University of Applied Sciences Leiden (NL), Helsinki University Hospital (FI), Karolinska Institutet (SE)
Target ALS, EU Joint Programme – Neurodegenerative Disease Research, Suomen Kulttuurirahasto, Karolinska Institutet, Vetenskapsrådet, Suomalainen Lääkäriseura Duodecim
Good health and well-being
Openalex Percentile: Top 14%
Amyotrophic Lateral Sclerosis Research
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