抄録
CD5 is constitutively expressed on all T cells and is a negative regulator of lymphocyte function. However, the full extent of CD5 function in immunity remains unclear. CD5 deficiency impacts thymic selection and extra-thymic regulatory T cell generation, yet CD5 knockout was reported to cause no immune pathology. Here we show that CD5 is a key modulator of gut immunity. We generated mice with inducible CD5 knockdown (KD) in the autoimmune-prone nonobese diabetic (NOD) background. CD5 deficiency caused T cell-dependent wasting disease driven by chronic gut immune dysregulation. CD5 inhibition also exacerbated acute experimental colitis. Mechanistically, loss of CD5 increased phospho-Stat3 levels, leading to elevated IL-17A secretion. Our data reveal a new facet of CD5 function in shaping the T cell cytokine profile.
| 本文言語 | 英語 |
|---|---|
| 論文番号 | 906499 |
| ジャーナル | Frontiers in Immunology |
| 巻 | 13 |
| DOI | |
| 出版ステータス | 出版済み - 02-06-2022 |
| 外部発表 | はい |
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All Science Journal Classification (ASJC) codes
- 免疫アレルギー学
- 免疫学
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