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IL-27/IL-27R Mediates Protective Immunity against Chlamydial Infection by Suppressing Excessive Th17 Responses and Reducing Neutrophil Inflammation
Author(s) -
Xiaoyu Zha,
Shuaini Yang,
Wenhao Niu,
Lu Tan,
Yueyue Xu,
Jiajia Zeng,
Yingying Tang,
Lida Sun,
Gaoju Pang,
Sai Qiao,
Hong Zhang,
Tengli Liu,
Huili Zhao,
Ningbo Zheng,
Yongci Zhang,
Hong Bai
Publication year - 2021
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.2000957
Subject(s) - immunology , inflammation , immunity , chemokine , biology , cytokine , immune system
IL-27, a heterodimeric cytokine of the IL-12 family, has diverse influences on the development of multiple inflammatory diseases. In this study, we identified the protective role of IL-27/IL-27R in host defense agains Chlamydia muridarum respiratory infection and further investigated the immunological mechanism. Our results showed that IL-27 was involved in C. muridarum infection and that IL-27R knockout mice (WSX-1 -/- mice) suffered more severe disease, with greater body weight loss, higher chlamydial loads, and more severe inflammatory reactions in the lungs than C57BL/6 wild-type mice. There were excessive IL-17-producing CD4 + T cells and many more neutrophils, neutrophil-related proteins, cytokines, and chemokines in the lungs of WSX-1 -/- mice than in wild-type mice following C. muridarum infection. In addition, IL-17/IL-17A-blocking Ab treatment improved disease after C. muridarum infection in WSX-1 -/- mice. Overall, we conclude that IL-27/IL-27R mediates protective immunity during chlamydial respiratory infection in mice by suppressing excessive Th17 responses and reducing neutrophil inflammation.

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