T helper 2 Cytokines inhibit autophagic control of intracellular Mycobacterium tuberculosis

被引:404
作者
Harris, James
De Haro, Sergio A.
Master, Sharon S.
Keane, Joseph
Roberts, Esteban A.
Delgado, Monica
Deretic, Vojo
机构
[1] Univ New Mexico, Sch Med, Dept Mol Genet & Microbiol, Ctr Hlth Sci, Albuquerque, NM 87131 USA
[2] St James Hosp, Dublin 8, Ireland
[3] Univ Dublin Trinity Coll, Dublin 8, Ireland
[4] Univ New Mexico, Dept Cell Biol & Physiol, Albuquerque, NM 87131 USA
关键词
D O I
10.1016/j.immuni.2007.07.022
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Autophagy is a recently recognized immune effector mechanism against intracellular pathogens. The role of autophagy in innate immunity has been well established, but the extent of its regulation by the adaptive immune response is less well understood. The T helper 1 (Th1) cell cytokine IFN-gamma induces autophagy in macrophages to eliminate Mycobacterium tuberculosis. Here, we report that Th2 cytokines affect autophagy in macrophages and their ability to control intracellular M. tuberculosis. IL-4 and IL-13 abrogated autophagy and autophagymediated killing of intracellular mycobacteria in murine and human macrophages. Inhibition of starvation-induced autophagy by IL-4 and IL-13 was dependent on Akt signaling, whereas the inhibition of IFN-gamma-induced autophagy was Akt independent and signal transducer and activator of transcription 6 (STAT6) dependent. These findings establish a mechanism through which Th1-Th2 polarization differentially affects the immune control of intracellular pathogens.
引用
收藏
页码:505 / 517
页数:13
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