| Literature DB >> 25972479 |
Byung Hyun Kang1, Hyo Jin Park2, Hye In Yum1, Seung Pyo Park3, Jin Kyun Park4, Eun Ha Kang5, Jae-Il Lee6, Eun Bong Lee4, Chung-Gyu Park7, Kyeong Cheon Jung8, Seong Hoe Park9.
Abstract
Identification of intrathymic eomesodermin(+) (Eomes(+)) CD4 T cells creates a novel idea that there is more than one way for the generation of innate CD4 T cells. Promyelocytic leukemia zinc finger protein(+) T cells and natural Th17 cells are known to be generated by sensing a high and persistent TCR strength, whereas this is not the case for Eomes(+) CD4 T cells. These cells go through low-level signal during the entire maturation pathway, which subsequently leads to induction of high susceptibility to cytokine IL-4. This event seems to be a major determinant for the generation of this type of cell. These T cells are functionally equivalent to Th1 cells that are present in the periphery, and this event takes place both in transgenic and in wild-type mice. There is additional evidence that this type of Eomes(+) innate CD4 T cell is also present in human cord blood.Entities:
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Year: 2015 PMID: 25972479 PMCID: PMC4456632 DOI: 10.4049/jimmunol.1401628
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422