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Experimental & Molecular Medicine ; : 494-501, 2006.
Article in English | WPRIM | ID: wpr-181050

ABSTRACT

In a murine model of systemic lupus erythematosus (SLE)-like chronic graft-versus-host disease (cGVHD), donor CD8+T cells rapidly fall into anergy to host cells, while donor CD4+T cells hyperactivate B cells and break B-cell tolerance to self-Ags in the recipient mouse. The functional recovery of donor CD8+T cells can result in the conversion of cGVHD to acute GVHD (aGVHD), indicating that donor CD8+T-cell anergy is a restriction factor in the development of cGVHD. In this report, we present evidence that donor CD4+CD25+regulatory T cells (T(reg) cells) are critical in maintaining the donor CD8+T-cell anergy and thus suppressing the development of aGVHD in mice that are naturally prone to cGVHD. Our results provide a novel insight into the role of T(reg) cells in determining cGVHD versus aGVHD.


Subject(s)
Mice , Female , Animals , T-Lymphocytes, Regulatory/immunology , Mice, Inbred DBA , Interleukin-2 Receptor alpha Subunit/metabolism , Immune Tolerance/physiology , Graft vs Host Disease/immunology , Clonal Anergy/physiology , Chronic Disease , CD8-Positive T-Lymphocytes/immunology , CD4-Positive T-Lymphocytes/immunology
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