Unknown

Dataset Information

0

CD4(+) lymphoid tissue-inducer cells promote innate immunity in the gut.


ABSTRACT: Fetal CD4(+) lymphoid tissue inducer (LTi) cells play a critical role in the development of lymphoid tissues. Recent studies identified that LTi cells persist in adults and are related to a heterogeneous population of innate lymphoid cells that have been implicated in inflammatory responses. However, whether LTi cells contribute to protective immunity remains poorly defined. We demonstrate that after infection with Citrobacter rodentium, CD4(+) LTi cells were a dominant source of interleukin-22 (IL-22) early during infection. Infection-induced CD4(+) LTi cell responses were IL-23 dependent, and ablation of IL-23 impaired innate immunity. Further, depletion of CD4(+) LTi cells abrogated infection-induced expression of IL-22 and antimicrobial peptides, resulting in exacerbated host mortality. LTi cells were also found to be essential for host protective immunity in lymphocyte-replete hosts. Collectively these data demonstrate that adult CD4(+) LTi cells are a critical source of IL-22 and identify a previously unrecognized function for CD4(+) LTi cells in promoting innate immunity in the intestine.

SUBMITTER: Sonnenberg GF 

PROVIDER: S-EPMC3035987 | biostudies-literature | 2011 Jan

REPOSITORIES: biostudies-literature

altmetric image

Publications

CD4(+) lymphoid tissue-inducer cells promote innate immunity in the gut.

Sonnenberg Gregory F GF   Monticelli Laurel A LA   Elloso M Merle MM   Fouser Lynette A LA   Artis David D  

Immunity 20101230 1


Fetal CD4(+) lymphoid tissue inducer (LTi) cells play a critical role in the development of lymphoid tissues. Recent studies identified that LTi cells persist in adults and are related to a heterogeneous population of innate lymphoid cells that have been implicated in inflammatory responses. However, whether LTi cells contribute to protective immunity remains poorly defined. We demonstrate that after infection with Citrobacter rodentium, CD4(+) LTi cells were a dominant source of interleukin-22  ...[more]

Similar Datasets

| S-EPMC3442242 | biostudies-literature
| S-EPMC2626689 | biostudies-literature
| S-EPMC3320042 | biostudies-literature
| S-EPMC3268875 | biostudies-literature
| S-EPMC6901086 | biostudies-literature
| S-EPMC6189280 | biostudies-literature
| S-EPMC4264842 | biostudies-literature
| S-EPMC4755916 | biostudies-literature
| S-EPMC4447235 | biostudies-literature
| S-EPMC6646407 | biostudies-literature