Mucosal-associated invariant T cells are numerically and functionally deficient in patients with mycobacterial infection and reflect disease activity

被引:84
|
作者
Kwon, Yong-Soo [1 ]
Cho, Young-Nan [2 ]
Kim, Moon-Ju [2 ]
Jin, Hye-Mi [2 ]
Jung, Hyun-Ju [2 ]
Kang, Jeong-Hwa [2 ]
Park, Ki-Jeong [2 ]
Kim, Tae-Jong [2 ]
Kee, Hae Jin [3 ]
Kim, Nacksung [4 ]
Kee, Seung-Jung [5 ]
Park, Yong-Wook [2 ]
机构
[1] Chonnam Natl Univ, Med Sch & Hosp, Dept Pulm & Crit Care Med, Gwangju 501757, South Korea
[2] Chonnam Natl Univ, Med Sch & Hosp, Dept Rheumatol, Gwangju 501757, South Korea
[3] Chonnam Natl Univ Hosp, Heart Res Ctr, Gwangju, South Korea
[4] Chonnam Natl Univ, Sch Med, Dept Pharmacol, Gwangju 501757, South Korea
[5] Chonnam Natl Univ, Med Sch & Hosp, Dept Lab Med, Gwangju 501757, South Korea
基金
新加坡国家研究基金会;
关键词
Mycobacterium tuberculosis; Nontuberculous mycobacteria; Mucosal-associated invariant T cells; Programmed death-1; VITAMIN-B METABOLITES; NONTUBERCULOUS MYCOBACTERIA; MAIT CELLS; DYSFUNCTION; PD-1;
D O I
10.1016/j.tube.2015.03.004
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Mucosal-associated invariant T (MAIT) cells contribute to protection against certain microorganism infections. The aims of this study were to examine the levels of MAIT cells in pulmonary tuberculosis (TB) and nontuberculous mycobacteria (NTM) lung disease patients, to evaluate the clinical relevance of MAIT cell levels, and to investigate the functions of MAIT cells. Patients with pulmonary TB (n = 35), NTM (n = 29), and healthy controls (n = 75) were enrolled in the study. MAIT cell levels and functions were measured by flow cytometry. Circluating MAIT cell levels were found to be reduced in TB and NTM patients. MAIT cell deficiency reflects a variety of clinical conditions. In particular, MAIT cell numbers were significantly correlated with sputum AFB positivity, extent of disease, hemoglobin levels, lymphocyte counts, CRP and ESR levels. MAIT cells in TB patients failed to produce interferon-gamma irrespective of the mode of stimulation, whereas NTM patients displayed a defect in MR1-dependent signaling pathway. Notably, an elevated expression of programmed death-1 was also associated with MAIT cell deficiency in TB. This study shows that MAIT cells are numerically and functionally deficient in TB and NTM patients and these deficiencies could contribute to immune system dysreguation in mycobacterial infection. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:267 / 274
页数:8
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