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.
MeSH Terms
Antibodies, Monoclonal/immunology
Antigens, Differentiation, T-Lymphocyte/immunology
CD3 Complex
CD4 Antigens/immunology
Cells, Cultured
Collagen/pharmacology
Humans
Integrins/immunology
Lymphocyte Activation/drug effects
Receptors, Antigen, T-Cell/immunology
Receptors, Cell Surface/immunology
Receptors, Collagen
Receptors, Very Late Antigen/immunology
T-Lymphocytes, Helper-Inducer/drug effects,immunology
Chemicals
Antibodies, Monoclonal
Antigens, Differentiation, T-Lymphocyte
CD3 Complex
CD4 Antigens
Integrins
Receptors, Antigen, T-Cell
Receptors, Cell Surface
Receptors, Collagen
Receptors, Very Late Antigen
Collagen
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Dang N H
Division of Tumor Immunology, Dana-Farber Cancer Institute, Boston, Massachusetts 02115.
Torimoto Y
Schlossman S F
Morimoto C
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