Circulating MAIT cells in multiple sclerosis and amyotrophic lateral sclerosis

被引:1
|
作者
De Federicis, Davide [1 ,2 ]
Bassani, Claudia [1 ,2 ]
Chiarelli, Rosaria Rita [1 ,2 ]
Montini, Federico [1 ,2 ,3 ]
Giordano, Antonino [1 ,2 ,3 ]
Esposito, Federica [1 ,2 ,3 ]
Riva, Nilo [1 ,2 ,3 ]
Quattrini, Angelo [1 ,2 ]
Martinelli, Vittorio [1 ,2 ,3 ]
Filippi, Massimo [1 ,2 ,3 ,4 ,5 ]
Farina, Cinthia [1 ,2 ]
机构
[1] Ist Sci San Raffaele, Inst Expt Neurol, Milan, Italy
[2] Ist Sci San Raffaele, Div Neurosci, Milan, Italy
[3] Ist Ricovero & Cura Carattere Sci, San Raffaele Sci Inst, Div Neurosci, Neurol Unit, Milan, Italy
[4] Ist Ricovero & Cura Carattere Sci, San Raffaele Sci Inst, Neurophysiol Serv, Milan, Italy
[5] Univ Vita Salute San Raffaele, Milan, Italy
来源
FRONTIERS IN IMMUNOLOGY | 2024年 / 15卷
关键词
amyotrophic lateral sclerosis; blood; CD161; MAIT cells; progressive multiple sclerosis; INVARIANT T-CELLS; DIAGNOSIS; POPULATION; DEFINES;
D O I
10.3389/fimmu.2024.1436717
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Neurological disorders, including multiple sclerosis (MS) and amyotrophic lateral sclerosis (ALS), may be associated with alterations in blood cell composition and phenotype. Here, we focused our attention on circulating mucosal-associated invariant T (MAIT) cells, a CD8+ T cell memory population expressing the invariant V alpha 7.2 region in the T cell receptor and high surface levels of the CD161 marker. Transcriptomics data relative to peripheral blood mononuclear cells (PBMC) highlighted downregulation of CD161 and other MAIT-associated markers in progressive MS and not relapsing remitting (RR)-MS when gene expressions relative to each disease course were compared to those from healthy controls. Multiparametric flow cytometry of freshly isolated PBMC samples from untreated RR-MS, primary or secondary progressive MS (PP- or SP-MS), ALS and age- and sex-matched healthy controls revealed specific loss of circulating CD8+ MAIT cells in PP-MS and no other MS courses or another neurological disorder such as ALS. Overall, these observations point to the existence of immunological changes in blood specific for the primary progressive course of MS that may support clinical definition of disease.
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页数:6
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