Interleukin 12p40 is required for dendritic cell migration and T cell priming after Mycobacterium tuberculosis infection

被引:254
作者
Khader, Shabaana A.
Partida-Sanchez, Santiago
Bell, Guy
Jelley-Gibbs, Dawn M.
Swain, Susan
Pearl, John E.
Ghilardi, Nico
deSauvage, Frederic J.
Lund, Frances E.
Cooper, Andrea M. [1 ]
机构
[1] Trudeau Inst Inc, Saranac Lake, NY 12983 USA
[2] Genentech Inc, San Francisco, CA 94080 USA
关键词
D O I
10.1084/jem.20052545
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Migration of dendritic cells (DCs) to the draining lymph node (DLN) is required for the activation of naive T cells. We show here that migration of DCs from the lung to the DLN after Mycobacterium tuberculosis (Mtb) exposure is defective in mice lacking interleukin (IL)-12p40. This defect compromises the ability of IL-12p40-deficient DCs to activate naive T cells in vivo; however, DCs that express IL-12p40 alone can activate naive T cells. Treatment of IL-12p40-deficient DCs with IL-12p40 homodimer (IL-12(p40) 2) restores Mtb-induced DC migration and the ability of IL-12p40-deficient DCs to activate naive T cells. These data define a novel and fundamental role for IL-12p40 in the pathogen-induced activation of pulmonary DCs.
引用
收藏
页码:1805 / 1815
页数:11
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