Literature DB >> 12818166

B7S1, a novel B7 family member that negatively regulates T cell activation.

Durbaka V R Prasad1, Sabrina Richards, Xoi Muoi Mai, Chen Dong.   

Abstract

T cell activation by antigen-presenting cells (APC) is regulated by positive and negative costimulatory molecules in the B7 family. Here we describe a novel addition in this family, designated as B7S1, which is uniquely anchored to the cell membrane via a GPI linkage. B7S1 is expressed on professional APC and widely distributed in nonlymphoid tissues. A soluble B7S1-Ig fusion protein binds to activated but not naive T cells. B7S1-Ig inhibits T cell activation and IL-2 production. A monoclonal antibody that blocks binding of B7S1 to its receptor enhances T cell proliferation in vitro and exacerbates experimental autoimmune encephalomyelitis in vivo. This study identifies a novel negative regulator of T cell activation and further reveals complex costimulatory regulation of immune responses.

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Year:  2003        PMID: 12818166     DOI: 10.1016/s1074-7613(03)00147-x

Source DB:  PubMed          Journal:  Immunity        ISSN: 1074-7613            Impact factor:   31.745


  164 in total

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5.  Tumor Regression and Delayed Onset Toxicity Following B7-H4 CAR T Cell Therapy.

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6.  BTNL2, a butyrophilin-like molecule that functions to inhibit T cell activation.

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Review 7.  Dendritic cell-mediated T cell polarization.

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8.  T-cell tolerance or function is determined by combinatorial costimulatory signals.

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Review 9.  The role of B7 family molecules in hematologic malignancy.

Authors:  Paul Greaves; John G Gribben
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10.  Expression of costimulatory molecules B7-H1, B7-H4 and Foxp3+ Tregs in gastric cancer and its clinical significance.

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