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Publication : The B7 family member B7-H3 preferentially down-regulates T helper type 1-mediated immune responses.

First Author  Suh WK Year  2003
Journal  Nat Immunol Volume  4
Issue  9 Pages  899-906
PubMed ID  12925852 Mgi Jnum  J:84973
Mgi Id  MGI:2671029 Doi  10.1038/ni967
Citation  Suh WK, et al. (2003) The B7 family member B7-H3 preferentially down-regulates T helper type 1-mediated immune responses. Nat Immunol 4(9):899-906
abstractText  We investigated the in vivo function of the B7 family member B7-H3 (also known as B7RP-2) by gene targeting. B7-H3 inhibited T cell proliferation mediated by antibody to T cell receptor or allogeneic antigen-presenting cells. B7-H3-deficient mice developed more severe airway inflammation than did wild-type mice in conditions in which T helper cells differentiated toward type 1 (T(H)1) rather than type 2 (T(H)2). B7-H3 expression was consistently enhanced by interferon-gamma but suppressed by interleukin 4 in dendritic cells. B7-H3-deficient mice developed experimental autoimmune encephalomyelitis several days earlier than their wild-type littermates, and accumulated higher concentrations of autoantibodies to DNA. Thus, B7-H3 is a negative regulator that preferentially affects T(H)1 responses.
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