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27. Transplantation immunology: organ and bone marrow.27. 移植免疫学:器官与骨髓
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本文引用的文献

1
Long-term clinical outcome of patients with severe combined immunodeficiency who received related donor bone marrow transplants without pretransplant chemotherapy or post-transplant GVHD prophylaxis.未接受移植前化疗或移植后移植物抗宿主病预防的严重联合免疫缺陷患者接受相关供体骨髓移植的长期临床结果。
J Pediatr. 2009 Dec;155(6):834-840.e1. doi: 10.1016/j.jpeds.2009.07.049. Epub 2009 Oct 9.
2
Nomenclature for factors of the HLA system, update June 2009.HLA系统因子命名法,2009年6月更新
Tissue Antigens. 2009 Oct;74(4):364-6. doi: 10.1111/j.1399-0039.2009.01330.x.
3
Overview of immunosuppression in liver transplantation.肝移植中的免疫抑制概述
World J Gastroenterol. 2009 Sep 14;15(34):4225-33. doi: 10.3748/wjg.15.4225.
4
Intestinal transplantation.肠道移植
N Engl J Med. 2009 Sep 3;361(10):998-1008. doi: 10.1056/NEJMra0804605.
5
Global observatory and database on donation and transplantation: world overview on transplantation activities.全球捐赠与移植观察站及数据库:移植活动的世界概况
Transplant Proc. 2009 Jul-Aug;41(6):2297-301. doi: 10.1016/j.transproceed.2009.05.004.
6
Standard graft-versus-host disease prophylaxis with or without anti-T-cell globulin in haematopoietic cell transplantation from matched unrelated donors: a randomised, open-label, multicentre phase 3 trial.在来自匹配无关供者的造血细胞移植中使用或不使用抗T细胞球蛋白进行标准移植物抗宿主病预防:一项随机、开放标签、多中心3期试验。
Lancet Oncol. 2009 Sep;10(9):855-64. doi: 10.1016/S1470-2045(09)70225-6. Epub 2009 Aug 18.
7
Long-term outcome of single pediatric donor kidney transplants between African-American and non-African-American adults.非裔美国成年人与非非裔美国成年人之间单例小儿供体肾移植的长期结果。
Clin Nephrol. 2009 Jul;72(1):55-61. doi: 10.5414/cnp72055.
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Safety profile and clinical outcomes in a phase I, placebo-controlled study of siplizumab in acute graft-versus-host disease.西普利单抗治疗急性移植物抗宿主病的I期安慰剂对照研究的安全性概况和临床结果
Transplantation. 2009 Jul 27;88(2):198-202. doi: 10.1097/TP.0b013e3181abfbf7.
9
The role of major histocompatibility complex class I chain-related gene A antibodies in organ transplantation.主要组织相容性复合体I类链相关基因A抗体在器官移植中的作用。
Curr Opin Organ Transplant. 2009 Aug;14(4):414-8. doi: 10.1097/mot.0b013e32832d835e.
10
Forty years of publication of transplantation proceedings--the second decade: the cyclosporine revolution.《移植会议论文集》出版四十年——第二个十年:环孢素革命
Transplant Proc. 2009 Jun;41(5):1423-37. doi: 10.1016/j.transproceed.2009.05.001.

移植免疫学:实体器官和骨髓。

Transplantation immunology: solid organ and bone marrow.

机构信息

Department of Pediatrics, Allergy/Immunology, Baylor College of Medicine, Houston, USA.

出版信息

J Allergy Clin Immunol. 2010 Feb;125(2 Suppl 2):S324-35. doi: 10.1016/j.jaci.2009.11.014.

DOI:10.1016/j.jaci.2009.11.014
PMID:20176267
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2857984/
Abstract

Development of the field of organ and tissue transplantation has accelerated remarkably since the human MHC was discovered in 1967. Matching of donor and recipient for MHC antigens has been shown to have a significant positive effect on graft acceptance. The roles of the different components of the immune system involved in the tolerance or rejection of grafts and in graft-versus-host disease have been clarified. These components include antibodies, antigen-presenting cells, helper and cytotoxic T-cell subsets, immune cell-surface molecules, signaling mechanisms, and cytokines. The development of pharmacologic and biological agents that interfere with the alloimmune response has had a crucial role in the success of organ transplantation. Combinations of these agents work synergistically, leading to lower doses of immunosuppressive drugs and reduced toxicity. Reports of significant numbers of successful solid-organ transplantations include those of the kidneys, liver, heart, and lung. The use of bone marrow transplantation for hematologic diseases, particularly hematologic malignancies and primary immunodeficiencies, has become the treatment of choice in many of these conditions. Other sources of hematopoietic stem cells are also being used, and diverse immunosuppressive drug regimens of reduced intensity are being proposed to circumvent the mortality associated with the toxicity of these drugs. Gene therapy to correct inherited diseases by means of infusion of gene-modified autologous hematopoietic stem cells has shown efficacy in 2 forms of severe combined immunodeficiency, providing an alternative to allogeneic tissue transplantation.

摘要

器官和组织移植领域自 1967 年人类 MHC 被发现以来发展迅速。供体和受者 MHC 抗原的匹配已被证明对移植物接受具有显著的积极影响。参与移植物耐受或排斥以及移植物抗宿主病的免疫系统的不同成分的作用已经阐明。这些成分包括抗体、抗原呈递细胞、辅助和细胞毒性 T 细胞亚群、免疫细胞表面分子、信号机制和细胞因子。干扰同种免疫反应的药理和生物制剂的发展在器官移植的成功中发挥了关键作用。这些药物联合使用具有协同作用,导致免疫抑制药物的剂量降低,毒性降低。成功进行实体器官移植的报告包括肾脏、肝脏、心脏和肺。骨髓移植用于血液疾病,特别是血液恶性肿瘤和原发性免疫缺陷,已成为许多此类疾病的首选治疗方法。其他来源的造血干细胞也在被使用,并且提出了不同强度的减少强度的免疫抑制药物方案,以避免与这些药物的毒性相关的死亡率。通过输注基因修饰的自体造血干细胞进行基因治疗以纠正遗传性疾病已在 2 种严重联合免疫缺陷中显示出疗效,为同种异体组织移植提供了替代方法。