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Autophagy protects against active tuberculosis by suppressing bacterial burden and inflammation.


ABSTRACT: Autophagy is a cell biological pathway affecting immune responses. In vitro, autophagy acts as a cell-autonomous defense against Mycobacterium tuberculosis, but its role in vivo is unknown. Here we show that autophagy plays a dual role against tuberculosis: antibacterial and anti-inflammatory. M. tuberculosis infection of Atg5(fl/fl) LysM-Cre(+) mice relative to autophagy-proficient littermates resulted in increased bacillary burden and excessive pulmonary inflammation characterized by neutrophil infiltration and IL-17 response with increased IL-1? levels. Macrophages from uninfected Atg5(fl/fl) LysM-Cre(+) mice displayed a cell-autonomous IL-1? hypersecretion phenotype, whereas T cells showed propensity toward IL-17 polarization during nonspecific activation or upon restimulation with mycobacterial antigens. Thus, autophagy acts in vivo by suppressing both M. tuberculosis growth and damaging inflammation.

SUBMITTER: Castillo EF 

PROVIDER: S-EPMC3503152 | biostudies-literature | 2012 Nov

REPOSITORIES: biostudies-literature

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Autophagy protects against active tuberculosis by suppressing bacterial burden and inflammation.

Castillo Eliseo F EF   Dekonenko Alexander A   Arko-Mensah John J   Mandell Michael A MA   Dupont Nicolas N   Jiang Shanya S   Delgado-Vargas Monica M   Timmins Graham S GS   Bhattacharya Dhruva D   Yang Hongliang H   Hutt Julie J   Lyons C Rick CR   Dobos Karen M KM   Deretic Vojo V  

Proceedings of the National Academy of Sciences of the United States of America 20121023 46


Autophagy is a cell biological pathway affecting immune responses. In vitro, autophagy acts as a cell-autonomous defense against Mycobacterium tuberculosis, but its role in vivo is unknown. Here we show that autophagy plays a dual role against tuberculosis: antibacterial and anti-inflammatory. M. tuberculosis infection of Atg5(fl/fl) LysM-Cre(+) mice relative to autophagy-proficient littermates resulted in increased bacillary burden and excessive pulmonary inflammation characterized by neutrophi  ...[more]

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