4.1 Review

Memory T-cell-specific therapeutics in organ transplantation

期刊

CURRENT OPINION IN ORGAN TRANSPLANTATION
卷 14, 期 6, 页码 643-649

出版社

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/MOT.0b013e328332bd4a

关键词

allograft; heterologous immunity; homeostatic proliferation; memory T cell; tolerance

资金

  1. National Institutes of Health [11 U01 A107922301A1, Al 079409]
  2. Georgia Research Alliance
  3. McKelvey Foundation
  4. Juvenile Diabetes Research Foundation

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Purpose of review This review details the role of memory T cells in physiologic and allospecific immunity, and summarizes the effects of immunosuppressive agents used to manipulate their function in the context of organ transplantation. Recent findings Memory T cells are lymphocytes with characteristics that are thought to promote anamnestic immune responses. They have a unique capacity to generate rapid effector functions upon secondary exposure to a pathogen, and this capacity is achieved through truncated requirements for antigen presentation, reduced activation thresholds, and enhanced trafficking and adhesion mechanisms. In general, these same mechanisms also appear to evoke improved efficiency in mediating allograft rejection. The phenotype of these cells has been increasingly well defined and associated with a characteristic pattern of susceptibility to immunosuppressive agents. This knowledge is now being exploited in the development of immune therapeutic regimens to selectively mollify T memory cell effects. Summary A specific targeting of memory T cells has potential to prevent allograft rejection in a more precise manner than current means of immunosuppression. However, these benefits will be balanced by the reciprocal risk of susceptibility to recurrent infection.

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