| Literature DB >> 11101875 |
A M Moodycliffe1, D Nghiem, G Clydesdale, S E Ullrich.
Abstract
Ultraviolet (UV) radiation is carcinogenic and immunosuppressive. UV-induced immune suppression is mediated by antigen-specific T cells, which can transfer suppression to normal recipients. These cells are essential for controlling skin cancer development in the UV-irradiated host and in suppressing other immune responses, such as delayed-type hypersensitivity. Despite their importance in skin cancer development, their exact identity has remained elusive. We show here that natural killer T cells from UV-irradiated donor mice function as suppressor T cells and play a critical role in regulating the growth of UV-induced skin cancers and suppressing adaptive immune responses in vivo.Entities:
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Year: 2000 PMID: 11101875 DOI: 10.1038/82782
Source DB: PubMed Journal: Nat Immunol ISSN: 1529-2908 Impact factor: 25.606