摘要
造血干细胞移植后绌胞免疫缺陷是疾病复发的一个重要原因,同时异基因造血干细胞移植也可以认为是一种过继性免疫治疗,能克服受者细胞免疫缺陷和促进移植物抗肿瘤(GVT)效应,清除微小残留病和预防疾病复发。如何提高GVT效应仍需要进一步明确,重点介绍2011年美国血液学会(ASH)年会上相关的新进展。
Cellular immunodeficiency is malignancy post stem cell transplantation. On the an important factor related to relapse of hematological other hand, allogeneic stem cell transplantation can be considered the adoptive immunotherapy, which can overcome the host immunodeficiency and promote graft- versus-tumor (GVT) effect for elimination of minimal residual disease and prevention of relapse. How to optimize the GVT induction is required to be defined more clearly. In this review, advance knowledge concerning the optimized and clinical setting of GVT induction from 2011 ASH annual meeting is summarized.
出处
《白血病.淋巴瘤》
CAS
2012年第1期3-5,12,共4页
Journal of Leukemia & Lymphoma
关键词
造血干细胞移植
异基因
移植物抗肿瘤
免疫疗法
过继
Hematopoietic stem cell transplantation, allogeneic
Graft versus tumor
Immunotherapy, adoptive