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. 1996 Feb;319(2):125-9.

Early defect of immunoregulatory T cells in autoimmune diabetes

J M Gombert  1 , A Herbelin, E Tancrède-Bohin, M Dy, L Chatenoud, C Carnaud, J F Bach
Affiliations
  • PMID: 8680958

Early defect of immunoregulatory T cells in autoimmune diabetes

J M Gombert et al. C R Acad Sci III. 1996 Feb.

Abstract

A potential immunoregulatory function has recently been attributed to the discrete subset of major histocompatibility complex (MHC) class I-restricted TCR-alpha beta mature thymocytes expressing an unusual V beta 8-biased T cell receptor repertoire. This T cell subset which also selectively express the CD44 marker is the main IL-4 producer in the thymus. Nonobese diabetic (NOD) mice were found to have a marked deficit in the number and functional capacity of CD44+ TCR-alpha beta+ thymocytes from as early as 3 weeks of age. The deficiency in IL-4 production was completely corrected after incubation with interleukin-7 (IL-7), a selective growth factor for CD44+ TCR-alpha beta+ mature thymocytes. This abnormality in T cell differentiation could explain the Th2 functional deficiency that may be a key element in the emergence of Th1-driven autoimmune disease in NOD mice.

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