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IL-26 contributes to host defense against intracellular bacteria.


ABSTRACT: IL-26 is an antimicrobial protein secreted by Th17 cells that has the ability to directly kill extracellular bacteria. To ascertain whether IL-26 contributes to host defense against intracellular bacteria, we studied leprosy, caused by the obligate intracellular pathogen Mycobacterium leprae, as a model. Analysis of leprosy skin lesions by gene expression profiling and immunohistology revealed that IL-26 was more strongly expressed in lesions from the self-limited tuberculoid compared with expression in progressive lepromatous patients. IL-26 directly bound to M. leprae in axenic culture and reduced bacteria viability. Furthermore, IL-26, when added to human monocyte-derived macrophages infected with M. leprae, entered the infected cell, colocalized with the bacterium, and reduced bacteria viability. In addition, IL-26 induced autophagy via the cytoplasmic DNA receptor stimulator of IFN genes (STING), as well as fusion of phagosomes containing bacilli with lysosomal compartments. Altogether, our data suggest that the Th17 cytokine IL-26 contributes to host defense against intracellular bacteria.

SUBMITTER: Dang AT 

PROVIDER: S-EPMC6486355 | biostudies-literature | 2019 Apr

REPOSITORIES: biostudies-literature

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IL-26 contributes to host defense against intracellular bacteria.

Dang Angeline Tilly AT   Teles Rosane Mb RM   Weiss David I DI   Parvatiyar Kislay K   Sarno Euzenir N EN   Ochoa Maria T MT   Cheng Genhong G   Gilliet Michel M   Bloom Barry R BR   Modlin Robert L RL  

The Journal of clinical investigation 20190402 5


IL-26 is an antimicrobial protein secreted by Th17 cells that has the ability to directly kill extracellular bacteria. To ascertain whether IL-26 contributes to host defense against intracellular bacteria, we studied leprosy, caused by the obligate intracellular pathogen Mycobacterium leprae, as a model. Analysis of leprosy skin lesions by gene expression profiling and immunohistology revealed that IL-26 was more strongly expressed in lesions from the self-limited tuberculoid compared with expre  ...[more]

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