Abstract
In the present study, we showed that activation of human CD4 T cells can be induced by anti-CD3 and collagen in a serum-free system. This activation was inhibited by the addition of peptides containing the RGD or Gly-Pro-X sequences. Significantly, we demonstrated that both the 1F7 (CD26) structure and the VLA integrin family, particularly the VLA-3 complex, contribute to the functional interaction between collagen and CD4 cells since anti-1F7 and anti-VLA-3 specifically inhibited this collagen-induced CD4 cell activation. Biochemical studies showed that the 1F7 structure is not a member of the VLA integrin family. These results thus indicated that two different families of antigens serve as functional collagen receptors for CD4 T cell activation.
Publication types
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Antibodies, Monoclonal / immunology
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Antigens, Differentiation, T-Lymphocyte / immunology
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CD3 Complex
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CD4 Antigens / immunology*
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Cells, Cultured
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Collagen / pharmacology
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Humans
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Integrins / immunology*
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Lymphocyte Activation* / drug effects
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Receptors, Antigen, T-Cell / immunology
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Receptors, Cell Surface / immunology*
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Receptors, Collagen
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Receptors, Very Late Antigen / immunology*
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T-Lymphocytes, Helper-Inducer / drug effects
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T-Lymphocytes, Helper-Inducer / immunology*
Substances
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Antibodies, Monoclonal
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Antigens, Differentiation, T-Lymphocyte
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CD3 Complex
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CD4 Antigens
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Integrins
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Receptors, Antigen, T-Cell
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Receptors, Cell Surface
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Receptors, Collagen
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Receptors, Very Late Antigen
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Collagen