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Autoimmune response to C9orf72 protein in amyotrophic lateral sclerosis
Journal article   Open access   Peer reviewed

Autoimmune response to C9orf72 protein in amyotrophic lateral sclerosis

Tanner Michaelis, Cecilia S Lindestam Arlehamn, Emil Johansson, April Frazier, James D Berry, Merit Cudkowicz, Namita A Goyal, Christina Fournier, Allison Snyder, Justin Y Kwan, …
Nature (London)
2025
PMID: 41034581
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CC BY-NC-ND V4.0 Open Access

Abstract

Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease characterized by a progressive loss of motor neurons. Neuroinflammation is apparent in affected tissues, including increased T cell infiltration and activation of microglia, particularly in the spinal cord . Autoimmune responses are thought to have a key role in ALS pathology, and it is hypothesized that T cells contribute to the rapid loss of neurons during disease progression . However, until now there has been no reported target for such an autoimmune response. Here we show that ALS is associated with recognition of the C9orf72 antigen, and we map the specific epitopes that are recognized. We show that these responses are mediated by CD4 T cells that preferentially release IL-5 and IL-10, and that IL-10-mediated T cell responses are significantly greater in donors who have a longer predicted survival time. Our results reinforce the previous hypothesis that neuroinflammation has an important role in ALS disease progression, possibly because of a disrupted balance of inflammatory and counter-inflammatory T cell responses . These findings highlight the potential of therapeutic strategies aimed at enhancing regulatory T cells , and identify a key target for antigen-specific T cell responses that could enable precision therapeutics in ALS.

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Source: InCites

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Collaboration types
Domestic collaboration
International collaboration
Citation topics
1 Clinical & Life Sciences
1.52 Neurodegenerative Diseases
1.52.765 ALS Mechanisms
Web Of Science research areas
Neurosciences
ESI research areas
Neuroscience & Behavior
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