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造血干细胞移植的免疫学

Immunology of hematopoietic stem cell transplant.

作者信息

Mosaad Youssef Mohamed

机构信息

Clinical Immunology Unit, Clinical Pathology Department & Mansoura Research Center for Cord Stem Cell (MARC-CSC), Mansoura Faculty of Medicine, Mansoura University , Mansoura , Egypt.

出版信息

Immunol Invest. 2014;43(8):858-87. doi: 10.3109/08820139.2014.942460.

Abstract

Hematopoietic stem cell transplantation (HSCT) is a procedure in which infusion of hematopoietic stem cells is used to reestablish hematopoietic function in patients with damaged or defective bone marrow or immune systems. Early and late complications following allogeneic HSCT include acute and chronic graft-versus-host disease (GVHD), donor rejection, graft failure, relapse of primary malignancy, conditioning-related toxicity, immunodeficiency and infections. Immunology has a central role in allogeneic hematopoietic cell transplantation. Any appreciation of the immunological mechanism involved in engraftment, GVHD, the development of tolerance, immune reconstitution, and the control of malignancy requires some understanding of the immunologic basis for immune reactions provoked by grafting tissue from one individual to another. In the future it should be possible to learn what gene(s) must be activated and which must be repressed to force stem cells into division without maturation; to engineer a mechanism into the cells that stops proliferation and sets the stage for amplification; to search if there could be a universal donor cell line, neatly packaged and stabilized in sealed vials and distributed by the pharmaceutical industry; to modify the transplanted cells in such a way that they have a proliferative advantage over those of the host and to deliver the lethal blow against the neoplasm, perhaps the cells that are infused will be engineered in such a way as to be able to distinguish between normal host cells and tumor.

摘要

造血干细胞移植(HSCT)是一种通过输注造血干细胞来重建骨髓或免疫系统受损或有缺陷患者造血功能的程序。异基因HSCT后的早期和晚期并发症包括急性和慢性移植物抗宿主病(GVHD)、供体排斥、移植物失败、原发性恶性肿瘤复发、预处理相关毒性、免疫缺陷和感染。免疫学在异基因造血细胞移植中起着核心作用。要理解移植、GVHD、耐受性发展、免疫重建和恶性肿瘤控制所涉及的免疫机制,需要对将一个个体的组织移植到另一个个体所引发的免疫反应的免疫学基础有一定的了解。未来应该有可能了解哪些基因必须被激活,哪些必须被抑制,才能迫使干细胞在不成熟的情况下进行分裂;在细胞中设计一种机制,阻止增殖并为扩增做好准备;寻找是否可能存在一种通用的供体细胞系,整齐地包装并稳定在密封小瓶中,由制药行业分发;以这样一种方式修饰移植细胞,使其比宿主细胞具有增殖优势,并对肿瘤给予致命一击,也许注入的细胞将被设计成能够区分正常宿主细胞和肿瘤细胞。

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