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pubmed-article:21584812pubmed:abstractTextMany hematological malignancies consist of tumor cells that are spontaneously recognized and killed by V?9V?2 T cells. These tumor cells generate high amounts of intracellular phosphorylated metabolites mimicking the natural ligands and display a wide range of stress-induced self-ligands that are recognized by V?9V?2 T cells via TCR-dependent and TCR-independent mechanisms. The intrinsic features of V?9V?2 T cells and that of tumor cells of hematological origin constitute an ideal combination from which to develop V?9V?2 T cell-based immune interventions. In this review, we will discuss the rationale, preclinical and clinical data in favor of this therapeutic strategy and the future perspectives of its development.lld:pubmed
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pubmed-article:21584812pubmed:authorpubmed-author:KIMU HUHlld:pubmed
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pubmed-article:21584812pubmed:year2011lld:pubmed
pubmed-article:21584812pubmed:articleTitleV?9V?2 T cell-based immunotherapy in hematological malignancies: from bench to bedside.lld:pubmed
pubmed-article:21584812pubmed:affiliationLaboratorio di Ematologia Oncologica, Centro di Ricerca in Medicina Sperimentale (CeRMS), and Divisione Universitaria di Ematologia, Ospedale San Giovanni Battista di Torino e Universita' degli Studi di Torino, Turin, Italy.lld:pubmed
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