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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.

DOI:10.3109/08820139.2014.942460
PMID:25296239
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。

相似文献

1
Immunology of hematopoietic stem cell transplant.造血干细胞移植的免疫学
Immunol Invest. 2014;43(8):858-87. doi: 10.3109/08820139.2014.942460.
2
Alloreactivity as therapeutic principle in the treatment of hematologic malignancies. Studies of clinical and immunologic aspects of allogeneic hematopoietic cell transplantation with nonmyeloablative conditioning.异基因反应性作为血液系统恶性肿瘤治疗的治疗原则。非清髓性预处理的异基因造血细胞移植的临床和免疫学方面的研究。
Dan Med Bull. 2007 May;54(2):112-39.
3
Hematopoietic stem cell graft manipulation as a mechanism of immunotherapy.造血干细胞移植操作作为一种免疫治疗机制。
Int Immunopharmacol. 2003 Aug;3(8):1121-43. doi: 10.1016/S1567-5769(03)00014-6.
4
Related HLA-mismatched/haploidentical hematopoietic stem cell transplantation without in vitro T-cell depletion: observations of a single Chinese center.无关供者HLA错配/单倍型相合非体外去除T细胞的造血干细胞移植:单中心中国经验
Clin Transpl. 2011:237-45.
5
[T-cell-depleted HLA non-identical bone marrow transplantation in the child: prevention of graft-versus-host reaction by administration of donor T lymphocytes alloreactive against the recipient].儿童中去除T细胞的HLA不相合骨髓移植:通过给予对受者具有同种异体反应性的供体T淋巴细胞预防移植物抗宿主反应
J Soc Biol. 2001;195(1):65-8.
6
Role of antithymocyte globulin and granulocyte-colony stimulating factor-mobilized bone marrow in allogeneic transplantation for patients with hematologic malignancies.抗胸腺细胞球蛋白和粒细胞集落刺激因子动员的骨髓在血液系统恶性肿瘤患者异基因移植中的作用。
Biol Blood Marrow Transplant. 2009 Feb;15(2):266-73. doi: 10.1016/j.bbmt.2008.11.029.
7
Nonmyeloablative stem cell transplantation and cell therapy for malignant and non-malignant diseases.非清髓性干细胞移植及针对恶性和非恶性疾病的细胞治疗
Transpl Immunol. 2005 Aug;14(3-4):207-19. doi: 10.1016/j.trim.2005.03.009. Epub 2005 Apr 26.
8
[Allogeneic hematopoietic stem-cell transplantation for hematological malignancies].[异基因造血干细胞移植治疗血液系统恶性肿瘤]
Bull Cancer. 2001 Sep;88(9):908-26.
9
Cotransplantation of HLA-identical sibling culture-expanded mesenchymal stem cells and hematopoietic stem cells in hematologic malignancy patients.在血液系统恶性肿瘤患者中共同移植人类白细胞抗原(HLA)匹配的同胞培养扩增间充质干细胞和造血干细胞。
Biol Blood Marrow Transplant. 2005 May;11(5):389-98. doi: 10.1016/j.bbmt.2005.02.001.
10
Expanded donor natural killer cell and IL-2, IL-15 treatment efficacy in allogeneic hematopoietic stem cell transplantation.扩增供体自然杀伤细胞及白细胞介素-2、白细胞介素-15在异基因造血干细胞移植中的治疗效果
Eur J Haematol. 2008 Sep;81(3):226-35. doi: 10.1111/j.1600-0609.2008.01108.x. Epub 2008 Jun 28.

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The Impact of Human Microbiotas in Hematopoietic Stem Cell and Organ Transplantation.人类微生物组在造血干细胞和器官移植中的影响。
Front Immunol. 2022 Jul 7;13:932228. doi: 10.3389/fimmu.2022.932228. eCollection 2022.
2
Optimizing allogeneic grafts in hematopoietic stem cell transplantation.优化造血干细胞移植中的同种异体移植物。
Stem Cells Transl Med. 2021 Nov;10 Suppl 2(Suppl 2):S41-S47. doi: 10.1002/sctm.20-0481.
3
DNA methylation dynamic of bone marrow hematopoietic stem cells after allogeneic transplantation.异基因移植后骨髓造血干细胞的 DNA 甲基化动态。
Stem Cell Res Ther. 2019 May 20;10(1):138. doi: 10.1186/s13287-019-1245-6.
4
Trajectories of Fasting Blood Glucose in Autologous Hematopoietic Cell Transplantation.自体造血细胞移植中空腹血糖的变化轨迹。
Cancer Nurs. 2019 Jul/Aug;42(4):307-313. doi: 10.1097/NCC.0000000000000627.
5
Apoptotic cell-based therapies for promoting transplantation tolerance.基于凋亡细胞的促进移植耐受疗法。
Curr Opin Organ Transplant. 2018 Oct;23(5):552-558. doi: 10.1097/MOT.0000000000000562.
6
Checkpoint Inhibition in Hodgkin Lymphoma: Saving the Best for Last?霍奇金淋巴瘤中的检查点抑制:把最好的留到最后?
Oncology (Williston Park). 2016 Oct 15;30(10):914-20.
7
Higher plasma bilirubin predicts veno-occlusive disease in early childhood undergoing hematopoietic stem cell transplantation with cyclosporine.较高的血浆胆红素可预测接受环孢素造血干细胞移植的幼儿发生静脉闭塞性疾病。
World J Transplant. 2016 Jun 24;6(2):403-10. doi: 10.5500/wjt.v6.i2.403.