Pathogen-specific regulatory T cells delay the arrival of effector T cells in the lung during early tuberculosis

被引:245
作者
Shafiani, Shahin [1 ]
Tucker-Heard, Glady's [1 ]
Kariyone, Ai [3 ]
Takatsu, Kiyoshi [3 ]
Urdahl, Kevin B. [1 ,2 ]
机构
[1] Univ Washington, Dept Pediat, Seattle, WA 98195 USA
[2] Univ Washington, Dept Immunol, Seattle, WA 98195 USA
[3] Univ Tokyo, Dept Microbiol & Immunol, Tokyo 1088639, Japan
基金
美国国家卫生研究院;
关键词
TRANSCRIPTION FACTOR FOXP3; INTERFERON-GAMMA RESPONSE; MYCOBACTERIUM-TUBERCULOSIS; DENDRITIC CELLS; IMMUNE-RESPONSES; VIRAL-INFECTION; TRANSGENIC MICE; BCG VACCINATION; RETINOIC-ACID; REG-CELLS;
D O I
10.1084/jem.20091885
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The ability of the adaptive immune system to restrict Mycobacterium tuberculosis (Mtb) is impeded by activated Foxp3(+) regulatory T (T reg) cells. The importance of pathogen-specific T reg cells in this process has not been addressed. We show that T reg cell expansion after aerosol Mtb infection does not occur until Mtb is transported to the pulmonary lymph node (pLN), and Mtb-specific T reg cells have an increased propensity to proliferate. Even small numbers of Mtb-specific T reg cells are capable of delaying the priming of effector CD4(+) and CD8(+) T cells in the pLN and their subsequent accumulation in the lung, the primary site of infection. This delay likely prolongs the initial phase of bacterial expansion and explains the higher bacterial burden observed in these mice. Thus, T reg cells recognizing Mtb-derived antigens specifically and potently restrict protective immune responses during tuberculosis.
引用
收藏
页码:1409 / 1420
页数:12
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