Abstract

Regulation of immune reactions is critical in ealth and disease. Nowhere is this clearer than folowing allogeneic hematopoietic cell transplantation HCT). Here the beneficial effects of graft-versusumor reactions are clearly demonstrated, as well as he detrimental morbidity and mortality of unconrolled graft-versus-host disease (GVHD). Control of mmune reactions is complex and involves many facors including blood flow, micro-environmental interctions, cytokines, chemokines and both pro-inflamatory and anti-inflammatory molecules. In addition t has become well recognized that specialized popuations of cells, termed regulatory T cells, are critically nvolved in controlling immune reactions. Although he field of regulatory T cell biology has been exlored for many years, the more recent identification f specific populations of cells capable of regulating mmune responses with defined phenotype has opened ur re-examination of the potential impact of these ellular populations on immune function. To date, a umber of different cell populations have been charcterized with defined ability to regulate immune rections, which include two major cell populations, amely those of CD4 CD25 regulatory T cells Treg) [1] and abTCR NK-T cells which express an nvariant T cell receptor and are CD1 reactive [2]. hese cellular populations have generated enormous nterest in the field of HCT since animal models have emonstrated the potential benefit of regulatory T ell biology.

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