| Literature DB >> 1902501 |
N Nakano1, H Kikutani, H Nishimoto, T Kishimoto.
Abstract
Five islet-reactive T cell clones were established from islet-infiltrating T cells of non-obese diabetic (NOD) mice. All clones expressed CD4, but not CD8, and responded to islet cells from various strains of mice in the context of I-ANOD. They could induce insulitis when transferred into disease-resistant I-E+ transgenic NOD mice. The T cell receptor (TCR) sequences utilized by the clones were determined. Their usage of TCR V and J segments was not restricted but was rather diverse. One of the clones utilized V beta 16. The expression of V beta 16 was significantly reduced in I-E+ transgenic NOD, suggesting the possibility that the islet-reactive T cell clone expressing V beta 16 may be deleted or inactivated by I-E molecules. This clone might be one of the candidates that triggers insulitis.Entities:
Mesh:
Substances:
Year: 1991 PMID: 1902501 PMCID: PMC2118862 DOI: 10.1084/jem.173.5.1091
Source DB: PubMed Journal: J Exp Med ISSN: 0022-1007 Impact factor: 14.307