Published in Oncology Business Week, March 12th, 2006
According to researchers in the United States, "The fate of tumor-specific CD4+ T cells is central to the outcome of the host immune response to cancer. We show that tumor antigen recognition by a subset of CD4+ T cells led to their differentiation into cells capable of suppressing naive and Th1 effector cells."
"Such tumor-induced regulatory T cells (TMTregs) arose both from precommitted 'natural' regulatory T cells and CD4+CD25-GITRlow precursors," said Gang Zhou and colleagues at Johns Hopkins University. "Once induced, TMTregs were capable of maintaining suppressor...
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