نتایج جستجو برای: diabetogenic

تعداد نتایج: 1108  

Journal: :Journal of immunology 2004
David V Serreze T Matthew Holl Michele P Marron Robert T Graser Ellis A Johnson Caroline Choisy-Rossi Robyn M Slattery Scott M Lieberman Teresa P DiLorenzo

Development of autoreactive CD4 T cells contributing to type 1 diabetes (T1D) in both humans and nonobese diabetic (NOD) mice is either promoted or dominantly inhibited by particular MHC class II variants. In addition, it is now clear that when co-expressed with other susceptibility genes, some common MHC class I variants aberrantly mediate autoreactive CD8 T cell responses also essential to T1...

Journal: :Journal of immunology 2002
Osami Kanagawa Ana Militech Barbala A Vaupel

Nonobese diabetic (NOD) mice carrying a transgenic TCR from an islet Ag-specific CD4 T cell clone, BDC2.5, do not develop diabetes. In contrast, the same transgenic NOD mice on the SCID background develop diabetes within 4 wk after birth. Using a newly developed mAb specific for the BDC2.5 TCR, we examined the interaction between diabetogenic T cells and regulatory T cells in NOD.BDC transgenic...

Journal: :Journal of immunology 1999
S Ramanathan P Poussier

One of the diabetes susceptibility genes of the BB/W (Biobreeding/Worcester) rat maps to the lyp locus on chromosome 4. The BB/W lyp allele is responsible for a severe peripheral T lymphopenia. Correction of this lymphopenia by transfer of normal, histocompatible T cells prevents diabetes, providing T cell reconstitution is initiated before insulitis. We have analyzed this time-dependent regula...

2017
John P. Driver Jeremy J. Racine Cheng Ye Deanna J. Lamont Brittney N. Newby Caroline M. Leeth Harold D. Chapman Todd M. Brusko Yi-Guang Chen Clayton E. Mathews David V. Serreze

Type 1 diabetes development in the NOD mouse model is widely reported to be dependent on high-level production by autoreactive CD4+ and CD8+ T cells of interferon-γ (IFN-γ), generally considered a proinflammatory cytokine. However, IFN-γ can also participate in tolerance-induction pathways, indicating it is not solely proinflammatory. This study addresses how IFN-γ can suppress activation of di...

Journal: :American journal of physiology. Endocrinology and metabolism 2002
Sandra A Schreyer Cynthia Vick Theodore C Lystig Paul Mystkowski Renée C LeBoeuf

The aim of this study was to determine whether phenotypes associated with type 2 diabetes are altered in dyslipidemic obese mice. C57BL/6 wild-type, low-density lipoprotein (LDL) receptor-deficient (LDLR-/-), and apolipoprotein E-deficient (apoE-/-) mice were fed a high-fat, high-carbohydrate diet (diabetogenic diet), and the development of obesity, diabetes, and hypertriglyceridemia was examin...

Journal: :Journal of immunology 2005
Thibault Griseri Lucie Beaudoin Jan Novak Lennart T Mars Françoise Lepault Roland Liblau Agnès Lehuen

Invariant NKT (iNKT) cells have been implicated in the regulation of autoimmune diseases. In several models of type 1 diabetes, increasing the number of iNKT cells prevents the development of disease. Because CD8 T cells play a crucial role in the pathogenesis of diabetes, we have investigated the influence of iNKT cells on diabetogenic CD8 T cells. In the present study, type 1 diabetes was ind...

2003

Intravenous injection of alloxan into rabbits, rats, dogs, monkeys, etc., produces a brief hyperglycemia, then a transient hypoglycemia, which in the case of rabbits is severe enough to cause convulsions and death, unless counteracted by repeated injections of glucose, and finally a permanent diabetic hyperglycemia. The cause of the transient hypoglycemia has had various explanations. Goldner a...

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