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同种异体造血干细胞移植中的特异性过继细胞免疫治疗。

Specific Adoptive Cellular Immunotherapy in Allogeneic Stem Cell Transplantation.

机构信息

Medizinische Klinik III, Klinikum rechts der Isar, Technische Universität München, Munich, Germany.

出版信息

Oncol Res Treat. 2017;40(11):691-696. doi: 10.1159/000484051. Epub 2017 Oct 26.

Abstract

Allogeneic hematopoietic stem cell transplantation (allo-HSCT) represents a treatment option for a diversity of advanced hematopoietic malignancies providing hope for long-term responses especially due to immunogenic effects associated with the treatment modality. Despite respectable progress in the field, relapses and/or opportunistic infections are major reasons for the high treatment-related mortality. However, a number of novel immunotherapeutic approaches using defined cell populations have been developed to directly target residual malignant cells as well as defined infectious diseases. We here provide an overview of current adoptive cellular immunotherapies in the context of allo-HSCT and close with an outlook on new directions within the field.

摘要

异基因造血干细胞移植(allo-HSCT)为多种晚期血液恶性肿瘤提供了一种治疗选择,为长期缓解带来了希望,尤其是因为该治疗方式与免疫原性效应相关。尽管该领域取得了可观的进展,但复发和/或机会性感染仍是导致高治疗相关死亡率的主要原因。然而,已经开发了许多使用定义明确的细胞群体的新型免疫治疗方法,以直接靶向残留的恶性细胞和明确的传染病。在此,我们概述了 allo-HSCT 背景下当前的过继细胞免疫疗法,并展望了该领域的新方向。

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