干细胞
免疫学
移植
川地34
造血干细胞移植
CD19
造血
祖细胞
移植物抗宿主病
医学
癌症研究
抗原
生物
内科学
细胞生物学
作者
Kieran Sahasrabudhe,Mario Otto,Peiman Hematti,Vaishalee P. Kenkre
标识
DOI:10.1080/10428194.2018.1485905
摘要
Allogeneic hematopoietic stem cell transplantation is a curative option for patients with a variety of diseases. Transplantation from a related haploidentical donor is being increasingly utilized for patients who lack an available human leukocyte antigen matched related or unrelated donor. One of the strategies used for haploidentical transplants involves selective depletion of T cells expressing the αβ T cell receptor and CD19+ B cells prior to transplant. This allows for the removal of cells responsible for graft-versus-host disease and post-transplant lymphoproliferative disorder but maintains hematopoietic progenitor and stem cells for engraftment (CD34+ cells), as well as cells to elicit graft-versus-tumor effect and provide anti-infective activity (such as gamma-delta T cells and natural killer cells). The aim of this review article is to present and discuss the data available to date from studies utilizing this method of transplantation.
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