Department of Pediatrics, Allergy/Immunology, Baylor College of Medicine, Houston, USA.
J Allergy Clin Immunol. 2010 Feb;125(2 Suppl 2):S324-35. doi: 10.1016/j.jaci.2009.11.014.
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.
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。