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pubmed-article:20460483pubmed:abstractTextBlockade of CTL-associated antigen-4 (CTLA-4), an inhibitory immunomodulatory molecule on T cells, has been shown to enhance T-cell responses and induce tumor rejection, and a number of clinical trials with anti-CTLA-4 blocking monoclonal antibody (mAb) are under way. However, accumulating evidence indicates that anti-CTLA-4 mAb increases the number of CD4+CD25+Foxp3+ regulatory T cells (Treg) and that anti-CTLA4 mAb alone is often insufficient to reject established tumors in mice and humans. Thus, finding maneuvers to control Tregs and other immunosuppressive mechanisms remains a critical challenge.lld:pubmed
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pubmed-article:20460483pubmed:articleTitleTwo distinct mechanisms of augmented antitumor activity by modulation of immunostimulatory/inhibitory signals.lld:pubmed
pubmed-article:20460483pubmed:affiliationDepartment of Cancer Vaccine, Mie University Graduate School of Medicine, Mie, Japan.lld:pubmed
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