Mucosal-associated invariant T cells are depleted and functionally altered in patients with common variable immunodeficiency

被引:12
作者
Arduini, Serena [1 ]
Dunne, Jean [2 ]
Conlon, Niall [2 ]
Feighery, Conleth [1 ,2 ]
Doherty, Derek G. [1 ]
机构
[1] Trinity Coll Dublin, Sch Med, Discipline Immunol, Dublin, Ireland
[2] St James Hosp, Dept Immunol, Dublin, Ireland
关键词
CVID; MAIT cells; iNKT cells; gamma delta T cells; Innate immunity; ANTIBODY-DEFICIENCY SYNDROME; B-CELLS; MAIT CELLS; SUBSETS; DIFFERENTIATION; SECRETION; MR1;
D O I
10.1016/j.clim.2016.12.002
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Common variable immunodeficiency (CVID) is a primary immunoglobulin deficiency characterized by recurrent infections and complications, including autoimmunity, enteropathy, polyclonal lymphocytic infiltration or lymphoid malignancy. Innate T cells can support B cell maturation and antibody production. We investigated the numbers, phenotypes and functions of circulating B cell,.gamma delta T cell, invariant natural killer T (iNKT) cell and mucosal-associated invariant T (MAIT) cell subsets in 23 CVID patients and 27 healthy controls. Switched memory B cells and plasmablasts were depleted in CVID patients (p < 0.0001).gamma delta T cells were found at normal numbers, but iNKT and MALT cells were depleted (p < 0.0001 and p < 0.002). MAIT cells were especially low in patients with complicated CVID (p < 0.05). MAIT cells from patients appeared more activated and more frequently produced interleulcin-17A, interleukin-22 and tumor necrosis factor-alpha than MALT cells from healthy subjects in vitro. Thus, MAIT cell depletion and activation may contribute to immunodeficiency and complications associated with CVID. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:23 / 30
页数:8
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