Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Ian J. Thomas"'
Autor:
Antonis K. Moustakas, George K. Papadopoulos, Liliana G. Petrich de Marquesini, Ian J. Thomas, F. Susan Wong, Li Wen
Publikováno v:
European Journal of Immunology
Insulin-reactive CD8 T cells are amongst the earliest islet-infiltrating CD8 T cells in NOD mice. Cloned insulin B15-23-reactive cells (designated G9C8), restricted by H-2K(d), are highly diabetogenic. We used altered peptide ligands (APL) substitute
Autor:
F. Susan Wong, Sylvie Guerder, Ian J. Thomas, David C. Wraith, Richard M. Smith, Richard A. Flavell, Liliana G. Petrich de Marquesini, Li Wen, Rommel Ravanan
Publikováno v:
The Journal of Immunology. 179:5936-5946
CD80 and CD86 both costimulate T cell activation. Their individual effects in vivo are difficult to study as they are coordinately up-regulated on APCs. We have studied mice expressing rat insulin promoter (RIP)-CD80 and RIP-CD86 on the NOD and NOD.s
Publikováno v:
Diabetes. 54:2032-2040
The most important genetic susceptibility factor for type 1 diabetes is encoded in the major histocompatibility complex (MHC). The nonobese diabetic (NOD) mouse, which develops spontaneous diabetes, expresses H-2 g7 comprising the MHC class I molecul
Autor:
Li Wen, Stephen Chapman, Christopher Viret, Florence Susan Wong, Lai Khai Siew, Gwen S. Scott, Ian J. Thomas
Publikováno v:
Diabetes
OBJECTIVE We have previously reported a highly diabetogenic CD8 T-cell clone, G9C8, in the nonobese diabetic (NOD) mouse, specific to low-avidity insulin peptide B15-23, and cells responsive to this antigen are among the earliest islet infiltrates. W
Publikováno v:
The Journal of Immunology. 178:S227-S227
We have previously generated highly diabetogenic insulin-reactive CD8 T cell clones designated G9C8 from the NOD mouse. The aim of our study was to investigate T cell selection and activation of CD8 T cells from a TCR transgenic mouse expressing the