Buckley Rebecca H
Department of Pediatrics, Allergy/Immunology, Duke University Medical Center, 362 Jones Building (Campus Box 2898), Durham, NC 27710-0001, USA.
J Allergy Clin Immunol. 2003 Feb;111(2 Suppl):S733-44. doi: 10.1067/mai.2003.142.
The discovery of the human MHC in 1967 launched the field of organ and tissue transplantation. More than 800,000 such transplants have been performed during this time. Although matching of donor and recipient for MHC antigens was shown to be of great importance and continues to be so, the development of pharmacologic agents and antilymphocyte antibodies that interfere with the process of graft rejection has had a crucial role in the success of organ transplantation during the past 2 decades. Enormous progress has been made in understanding the immunologic mechanisms of graft rejection and of graft-versus-host disease. The roles of antibodies, antigen-presenting cells, helper and cytotoxic T cells, immune cell surface molecules, and signaling mechanisms and the cytokines they release have been clarified. This understanding is leading to the development of newer immunosuppressive agents targeting various components of the rejection process. Combinations of these agents work synergistically, leading to lower doses and reduced toxicity. Similarly, the development of effective T-cell depletion techniques has been of great importance for bone marrow transplantation when an HLA-identical sibling is not available. The major obstacle to the performance of solid organ transplantation currently is the shortage of donor organs.
1967年人类主要组织相容性复合体(MHC)的发现开创了器官和组织移植领域。在此期间,已经进行了超过80万次这样的移植。尽管供体和受体的MHC抗原匹配已被证明非常重要且仍然如此,但在过去20年中,干扰移植排斥过程的药物和抗淋巴细胞抗体的开发在器官移植的成功中发挥了关键作用。在理解移植排斥和移植物抗宿主病的免疫机制方面已经取得了巨大进展。抗体、抗原呈递细胞、辅助性和细胞毒性T细胞、免疫细胞表面分子以及信号传导机制和它们释放的细胞因子的作用已经得到阐明。这种理解正在导致开发针对排斥过程各个组成部分的新型免疫抑制剂。这些药物的组合协同作用,导致剂量降低和毒性降低。同样,当没有 HLA 相同的同胞时,有效的T细胞清除技术的发展对于骨髓移植非常重要。目前实体器官移植的主要障碍是供体器官短缺。