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NK Cell and CD4+FoxP3+Regulatory T Cell Based Therapies for Hematopoietic Stem Cell Engraftment

期刊

STEM CELLS INTERNATIONAL
卷 2016, 期 -, 页码 -

出版社

HINDAWI LTD
DOI: 10.1155/2016/9025835

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资金

  1. Fondazione Italiana per la Ricerca sul Cancro
  2. Associazione Italiana Contro le Leucemie-Linfomi e Mieloma
  3. Societa Italiana di Ematologia Sperimentale (SIES)
  4. American Society for Blood and Marrow Transplantation
  5. National Cancer Institute [CA49605, HL075462, R01 HL114591]
  6. National Heart, Lung and Blood Institute
  7. NATIONAL CANCER INSTITUTE [P01CA049605] Funding Source: NIH RePORTER
  8. NATIONAL HEART, LUNG, AND BLOOD INSTITUTE [P01HL075462, R01HL114591] Funding Source: NIH RePORTER
  9. Associazione Italiana per la Ricerca sul Cancro Funding Source: Custom

向作者/读者索取更多资源

Allogeneic hematopoietic cell transplantation (HCT) is a powerful therapy to treat multiple hematological diseases. The intensive conditioning regimens used to allow for donor hematopoietic stemcell (HSC) engraftment are often associated with severe toxicity, delayed immune reconstitution, life-threatening infections, and thus higher relapse rates. Additionally, due to the high incidence of graft versus host disease (GvHD), HCT protocols have evolved to prevent such disease that has a detrimental impact on antitumor and antiviral responses. Here, we analyzed the role of host T and natural killer (NK) cells in the rejection of donor HSC engraftment as well as the impact of donor regulatory T cells (Treg) and NK cells on HSC engraftment. We review some of the current strategies that utilize NK or Treg to improve allogeneic HCT therapy in order to accomplish better HSC engraftment and immune reconstitution and achieve a lower incidence of cancer relapse, opportunistic infections, and GvHD.

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