ICAM-1 co-stimulates target cells to facilitate antigen presentation
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作者:
Lebedeva, T
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机构:Thomas Jefferson Univ, Dept Microbiol & Immunol, Philadelphia, PA 19107 USA
Lebedeva, T
Dustin, ML
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机构:Thomas Jefferson Univ, Dept Microbiol & Immunol, Philadelphia, PA 19107 USA
Dustin, ML
Sykulev, Y
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Thomas Jefferson Univ, Dept Microbiol & Immunol, Philadelphia, PA 19107 USAThomas Jefferson Univ, Dept Microbiol & Immunol, Philadelphia, PA 19107 USA
Sykulev, Y
[1
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机构:
[1] Thomas Jefferson Univ, Dept Microbiol & Immunol, Philadelphia, PA 19107 USA
[2] Thomas Jefferson Univ, Kimmel Canc Inst, Philadelphia, PA 19107 USA
[3] NYU, Sch Med, Skirball Inst Biomol Med, New York, NY 10016 USA
Adhesion molecules are known to mediate cell-cell interactions, particularly those between T cells and antigen-presenting or target cells. Recent studies identified ICAM-1 as a co-stimulatory ligand that binds to lymphocyte function associated antigen-1 (LFA-1), thereby promoting the activation of T cells. As ICAM-1 is expressed on virtually any cell, it becomes a crucial molecule for the activation of CD8(+) T cells in the absence of co-stimulation provided by CD80 and CD86 molecules. In addition, ICAM-1 might function as cell-surface receptor, capable of initiating intracellular signaling. ICAM-1 is associated with other cell molecules, including MHC-I proteins, and our recent data show that productive engagement of ICAM-1 on target cells leads to recruitment of the MHC-I proteins to the contact area and enhances presentation of cognate peptide MHC-I complexes to cytotoxic T cells.