Cytotoxic CD8 <sup>+</sup> T lymphocytes expressing ALS-causing SOD1 mutant selectively trigger death of spinal motoneurons

Emmanuelle Coque(Inserm), Céline Salsac(Inserm), Gabriel Espinosa-Carrasco(Inserm), Béla Varga(Centre National de la Recherche Scientifique), Nicolas Degauque(Inserm), Marion Cadoux(Inserm), Roxane Crabé(Inserm), Anaïs Virenque(Inserm), Claire Soulard(Inserm), Julie K. Fierle(Ludwig Cancer Research), Alexandre Brodovitch(Aix-Marseille Université), Margot Libralato(Inserm), Attila G. Végh(HUN-REN Szegedi Biológiai Kutatóközpont), Stéphanie Ventéo(Inserm), Frédérique Scamps(Inserm), José Boucraut(Aix-Marseille Université), David Laplaud(Inserm), Javier Hernández(Inserm), Csilla Gergely(Centre National de la Recherche Scientifique), Thierry Vincent(Inserm), Cédric Raoul(Inserm)
Proceedings of the National Academy of Sciences
January 23, 2019
Cited by 135Open Access
Full Text

Abstract

Significance CD8 + T lymphocytes, which are typically devoted to eliminate malignant and infected cells, have been described in the central nervous system (CNS) of patients and mice with amyotrophic lateral sclerosis (ALS). However, their role in ALS pathogenesis has yet to be unraveled. Here, we show that ablation of CD8 + T cells in ALS mice increased the number of surviving motoneurons. CD8 + T cells expressing the ALS-causing superoxide dismutase-1 mutant protein recognize and selectively kill motoneurons in vitro. To exert their cytotoxic function, mutant CD8 + T cells required presentation of the antigen-MHC-I complex at the surface of the motoneurons. Analysis of T cell receptor diversity supports the evidence that self-reactive CD8 + T lymphocytes infiltrate the CNS of ALS mice to exert cytotoxic function.


Related Papers

No related papers found

Powered by citation graph analysis