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The tetraspanin CD9 is preferentially expressed on the human CD4 + CD45RA + naive T cell population and is involved in T cell activation
Author(s) -
KOBAYASHI H.,
HOSONO O.,
IWATA S.,
KAWASAKI H.,
KUWANA M.,
TANAKA H.,
DANG N. H.,
MORIMOTO C.
Publication year - 2004
Publication title -
clinical & experimental immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.329
H-Index - 135
eISSN - 1365-2249
pISSN - 0009-9104
DOI - 10.1111/j.1365-2249.2004.02494.x
Subject(s) - t cell , tetraspanin , biology , microbiology and biotechnology , population , cd80 , cd28 , antigen , streptamer , il 2 receptor , interleukin 21 , immunology , cell , cytotoxic t cell , cd40 , in vitro , immune system , medicine , biochemistry , genetics , environmental health
SUMMARY Human CD4 + T cells can be divided into reciprocal memory and naive T cell subsets based on their expression of CD45 isoforms and CD29/integrin beta1 subunit. To identify unique cell surface molecules on human T cells, we developed a new monoclonal antibody termed anti5H9. Binding of anti5H9 triggers a co‐stimulatory response in human peripheral blood T cells. Retrovirus‐mediated expression cloning has revealed that the antigen recognized by anti5H9 is identical to the tetraspanin CD9. We now show that human CD9 is preferentially expressed on the CD4 + CD45RA + naive T cell subset, and that CD9 + CD45RA + T cells respond preferentially to the recombinant beta 2 ‐glycoprotein I, compared to CD9 – CD45RA + T cells. Furthermore, anti5H9 inhibits both the recombinant beta 2 ‐glycoprotein I‐ and the recall antigen tetanus toxoid‐specific T cell proliferation. These results suggest that the tetraspanin CD9 plays an important role in T cell activation.

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