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Persistent deficiency of mucosal-associated invariant T cells during dermatomyositis.

Authors :
Cassius, Charles
Branchtein, Mylene
Battistella, Maxime
Amode, Reyhan
Lepelletier, Clémence
Jachiet, Marie
Masson, Adèle de
Frumholtz, Laure
Chasset, François
Amoura, Zahir
Mathian, Alexis
Samri, Assia
Monfort, Jean-Benoit
Bachmeyer, Claude
Bengoufa, Djaouida
Cordoliani, Florence
Bagot, Martine
Bensussan, Armand
Bouaziz, Jean-David
Buanec, Hélène Le
Source :
Rheumatology; Sep2020, Vol. 59 Issue 9, p2282-2286, 5p
Publication Year :
2020

Abstract

Objectives Mucosal-associated invariant T (MAIT) cells are innate-like lymphocytes that are important for antibacterial immunity and may have regulatory roles. MAIT cells are decreased during SLE. However, their frequencies and phenotype have not been investigated in DM. We studied MAIT cell frequencies and phenotype in DM patients with active and inactive disease (after treatment). Methods Peripheral blood flow cytometry analysis of MAIT cells was compared between DM (n  = 22), SLE (n  = 10), psoriasis (n  = 7) and atopic dermatitis (n  = 5) patients, and healthy controls (n  = 19). Results A dramatic decrease of circulating MAIT cell frequency was observed in active DM and SLE patients compared with healthy controls and other inflammatory skin diseases [active DM: median = 0.25% (interquartile range 0.19–0.6%), P  < 0.0001; active SLE: median = 0.61 (0.55–0.77), P  < 0.0001 vs healthy controls: 2.32% (1.18–4.45%)]. MAIT cells from active DM patients had an abnormal phenotype including increased expression of CD25 and cytotoxic T-lymphocyte-associated protein 4 that correlated with their low frequency in the blood. Conclusion In DM, peripheral blood MAIT cells are dramatically reduced and have an activated/exhausted phenotype that may be linked to increased activation-induced cell death. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
14620324
Volume :
59
Issue :
9
Database :
Complementary Index
Journal :
Rheumatology
Publication Type :
Academic Journal
Accession number :
145386499
Full Text :
https://doi.org/10.1093/rheumatology/kez564