Mycobacterium-Specific γ9δ2 T Cells Mediate Both Pathogen-Inhibitory and CD40 Ligand-Dependent Antigen Presentation Effects Important for Tuberculosis Immunity

被引:18
作者
Abate, Getahun [1 ]
Spencer, Charles T. [1 ,2 ,3 ]
Hamzabegovic, Fahreta [1 ]
Blazevic, Azra [1 ]
Xia, Mei [1 ]
Hoft, Daniel F. [1 ,2 ]
机构
[1] St Louis Univ, Dept Internal Med, Div Infect Dis Allergy & Immunol, St Louis, MO 63103 USA
[2] St Louis Univ, Dept Mol Microbiol & Immunol, St Louis, MO 63103 USA
[3] Univ Texas El Paso, Dept Biol Sci, El Paso, TX 79968 USA
基金
美国国家卫生研究院;
关键词
BACILLE CALMETTE-GUERIN; INTERFERON-GAMMA; DENDRITIC CELLS; PULMONARY TUBERCULOSIS; CYTOKINE PRODUCTION; TYPE-1; CYTOKINES; INFECTION; CD4(+); LYMPHOCYTES; EXPANSION;
D O I
10.1128/IAI.01262-15
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Numerous pathogens, including Mycobacterium tuberculosis, can activate human gamma(9)delta(2) T cells to proliferate and express effector mechanisms. gamma(9)delta(2) T cells can directly inhibit the growth of intracellular mycobacteria and may also act as antigen-presenting cells (APC). Despite evidence for gamma delta T cells having the capacity to function as APC, the mechanisms involved and importance of these effects on overall tuberculosis (TB) immunity are unknown. We prepared M. tuberculosis-specific gamma(9)delta(2) T cell lines to study their direct protective effects and APC functions for M. tuberculosis-specific alpha beta T cells. The direct inhibitory effects on intracellular mycobacteria were measured, and the enhancing effects on proliferative and effector responses of alpha beta T cells assessed. Furthermore, the importance of cell-to-cell contact and soluble products for gamma(9)delta(2) T cell effector responses and APC functions were investigated. We demonstrate, in addition to direct inhibitory effects on intracellular mycobacteria, the following: (i) gamma(9)delta(2) T cells enhance the expansion of M. tuberculosis-specific alpha beta T cells and increase the ability of alpha beta T cells to inhibit intracellular mycobacteria; (ii) although soluble mediators are critical for the direct inhibitory effects of gamma(9)delta(2) T cells, their APC functions do not require soluble mediators; (iii) the APC functions of gamma(9)delta(2) T cells involve cell-to-cell contact that is dependent on CD4(0)-CD40 ligand (CD40L) interactions; and (iv) fully activated CD4(+) alpha beta T cells and gamma(9)delta(2) T cells provide similar immune enhancing/APC functions for M. tuberculosis-specific T cells. These effector and helper effects of gamma(9)delta(2) T cells further indicate that these T cells should be considered important new targets for new TB vaccines.
引用
收藏
页码:580 / 589
页数:10
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