College of Natural Sciences, Department of Microbial, Cellular and Molecular Biology, Addis Ababa University, P.O. Box 1176, Addis Ababa, Ethiopia.
Department of Biology, Debre Berhan University, P.O. Box 445, Debre Berhan, Ethiopia.
J Immunol Res. 2018 Mar 5;2018:5986740. doi: 10.1155/2018/5986740. eCollection 2018.
Kidney transplantation remains the treatment of choice for end-stage renal failure. When the immune system of the recipient recognizes the transplanted kidney as a foreign object, graft rejection occurs. As part of the host immune defense mechanism, human leukocyte antigen (HLA) is a major challenge for graft rejection in transplantation therapy. The impact of HLA mismatches between the donor and the potential recipient prolongs the time for renal transplantation therapy, tethered to dialysis, latter reduces graft survival, and increases mortality. The formation of pretransplant alloantibodies against HLA class I and II molecules can be sensitized through exposures to blood transfusions, prior transplants, and pregnancy. These preformed HLA antibodies are associated with rejection in kidney transplantation. On the other hand, the development of de novo antibodies may increase the risk for acute and chronic rejections. Allograft rejection results from a complex interplay involving both the innate and the adaptive immune systems. Thus, further insights into the mechanisms of tissue rejection and the risk of HLA sensitization is crucial in developing new therapies that may blunt the immune system against transplanted organs. Therefore, the purpose of this review is to highlight facts about HLA and its sensitization, various mechanisms of allograft rejection, the current immunosuppressive approaches, and the directions for future therapy.
肾移植仍然是治疗终末期肾衰竭的首选方法。当受者的免疫系统将移植的肾脏识别为异物时,就会发生移植物排斥反应。作为宿主免疫防御机制的一部分,人类白细胞抗原(HLA)是移植治疗中移植物排斥的主要挑战。供体和潜在受者之间 HLA 错配的影响延长了肾移植治疗的时间,与透析相关,后者降低了移植物的存活率,并增加了死亡率。通过输血、先前的移植和怀孕,针对 HLA Ⅰ类和Ⅱ类分子的预存同种抗体可以被致敏。这些预先形成的 HLA 抗体与肾移植中的排斥反应有关。另一方面,新产生的抗体可能会增加急性和慢性排斥反应的风险。同种异体移植物排斥反应是由先天和适应性免疫系统的复杂相互作用引起的。因此,深入了解组织排斥反应的机制和 HLA 致敏的风险对于开发可能抑制免疫系统对抗移植器官的新疗法至关重要。因此,本综述的目的是强调关于 HLA 及其致敏、同种异体移植物排斥的各种机制、当前的免疫抑制方法以及未来治疗方向的事实。