Low expression of antigen-presenting and costimulatory molecules by lung cells from tuberculosis patients

被引:6
作者
Flores-Batista, V. C. S. [1 ]
Boechat, N. [1 ]
Lago, P. M. [1 ]
Lazzarini, L. C. [1 ]
Pessanha, L. R. [1 ]
Almeida, A. S.
Mafort, T. T. [1 ]
Kritski, A. L. [1 ]
Ho, J. L. [2 ]
Lapa-e-Silva, J. R. [1 ,2 ]
机构
[1] Univ Fed Rio de Janeiro, Inst Doencas Torax, Hosp Univ Clementino Fraga Filho, Lab Multidisciplinar Pesquisa, BR-20541590 Rio De Janeiro, RJ, Brazil
[2] Cornell Univ, Weill Med Coll, Div Int Med & Infect Dis, New York, NY USA
关键词
tuberculosis; costimulatory molecules; CD86; MHC class II; HLA-DR;
D O I
10.1590/S0100-879X2006005000141
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Costimulatory and antigen-presenting molecules are essential to the initiation of T cell immunity to mycobacteria. The present study analyzed by immunocytochemistry, using monoclonal antibodies and alkaline phosphatase-anti-alkaline phosphatase method, the frequency of costimulatory (CD86, CD40, CD40L, CD28, and CD152) and antigen-presenting (MHC class II and CD1) molecules expression on human lung cells recovered by sputum induction from tuberculosis ( TB) patients (N = 22) and non-TB controls (N = 17). TB cases showed a statistically significant lower percentage of HLA-DR+ cells than control subjects (21.9 +/- 4.2 vs 50.0 +/- 7.2%, P < 0.001), even though similar proportions of TB cases (18/22) and control subjects (16/17, P = 0.36) had HLA-DR-positive-stained cells. In addition, fewer TB cases (10/22) compared to control subjects (16/17) possessed CD86-expressing cells ( P = 0.04; OR: 0.05; 95% CI = 0.00-0.51), and TB cases expressed a lower percentage of CD86+ cells ( P = 0.04). Moreover, TB patients with clinically limited disease (= 1 lobe) on chest X-ray exhibited a lower percentage of CD86-bearing cells compared to patients with more extensive lung disease (> 1 lobe) ( P = 0.02). The lower expression by lung cells from TB patients of HLA-DR and CD86, molecules involved in antigen presentation and activation of T cells, may minimize T cell recognition of Mycobacterium tuberculosis, fostering an immune dysfunctional state and active TB.
引用
收藏
页码:1671 / 1679
页数:9
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