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    J Exp Med. 1996 Jan 1;183(1):67-76.

    CD8 T cell clones from young nonobese diabetic (NOD) islets can transfer rapid onset of diabetes in NOD mice in the absence of CD4 cells.

    Wong FS, Visintin I, Wen L, Flavell RA, Janeway CA Jr.

    Section of Immunobiology, Yale University School of Medicine, New Haven, Connecticut 06510, USA.

    T cells play an important role in the pathogenesis of diabetes in the nonobese diabetic (NOD) mouse. CD8 cytotoxic T cell lines and clones were generated from the lymphocytic infiltrate in the islets of Langerhans of young (7-wk-old). NOD mice by growing them on (NOD x B6-RIP-B7-1)F1 islets. These cells proliferate specifically to NOD islets and kill NOD islets in vitro. The cells are restricted by H-2Kd, and all bear T cell antigen receptor encoded by V beta 6. When these CD8 T cell lines and clones are adoptively transferred to irradiated female NOD, young NOD-SCID, and CB17-SCID mice, diabetes occurs very rapidly, within 10 d of transfer and without CD4 T cells.

    PMID: 8551245 [PubMed - indexed for MEDLINE]

    PMCID: 2192404

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