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Development of Antigen-Specific CD8+ CTL in MHC Class I-Deficient Mice through CD4 to CD8 Conversion
Author(s) -
Yasuhiro Tanaka,
Shigeo Koido,
JianChuan Xia,
Masaya Ohana,
Chunlei Liu,
Gregory M. Coté,
Douglas B. Sawyer,
Stuart K. Calderwood,
Jianlin Gong
Publication year - 2004
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.172.12.7848
Subject(s) - ctl* , cytotoxic t cell , cd8 , adoptive cell transfer , mhc class i , immunity , immunology , effector , antigen , biology , microbiology and biotechnology , t cell , immune system , in vitro , biochemistry
CD8+ CTL are the predominant tumoricidal effector cells. We find, however, that MHC class I-deficient mice depleted of CD8+ T cells are able to mount an effective antitumor immunity after immunization with fused dendritic/tumor cells. Such immunity appears to be mediated by the generation of phenotypic and functional CD8+ CTL through CD4+ to CD8+ conversion, which we have demonstrated at the single cell level. CD4+ to CD8+ conversion depends on effective in vivo activation and is promoted by CD4+ T cell proliferation. The effectiveness of this process is shown by the generation of antitumor immunity through adoptive transfer of primed CD4 T cells to provide protection against tumor cell challenge and to eliminate established pulmonary metastases.

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