Zachary Andrea A, Leffell Mary S
Department of Medicine, Johns Hopkins University School of Medicine , Baltimore, MD , USA.
Front Immunol. 2016 Dec 7;7:575. doi: 10.3389/fimmu.2016.00575. eCollection 2016.
HLA matching provides numerous benefits in organ transplantation including better graft function, fewer rejection episodes, longer graft survival, and the possibility of reduced immunosuppression. Mismatches are attended by more frequent rejection episodes that require increased immunosuppression that, in turn, can increase the risk of infection and malignancy. HLA mismatches also incur the risk of sensitization, which can reduce the opportunity and increase waiting time for a subsequent transplant. However, other factors such as donor age, donor type, and immunosuppression protocol, can affect the benefit derived from matching. Furthermore, finding a well-matched donor may not be possible for all patients and usually prolongs waiting time. Strategies to optimize transplantation for patients without a well-matched donor should take into account the immunologic barrier represented by different mismatches: what are the least immunogenic mismatches considering the patient's HLA phenotype; should repeated mismatches be avoided; is the patient sensitized to HLA and, if so, what are the strengths of the patient's antibodies? This information can then be used to define the HLA type of an immunologically optimal donor and the probability of such a donor occurring. A probability that is considered to be too low may require expanding the donor population through paired donation or modifying what is acceptable, which may require employing treatment to overcome immunologic barriers such as increased immunosuppression or desensitization. Thus, transplantation must strike a balance between the risk associated with waiting for the optimal donor and the risk associated with a less than optimal donor.
HLA配型在器官移植中具有诸多益处,包括更好的移植物功能、更少的排斥反应、更长的移植物存活时间以及降低免疫抑制的可能性。不匹配则伴随着更频繁的排斥反应,这需要增加免疫抑制,而这反过来又会增加感染和恶性肿瘤的风险。HLA不匹配还会带来致敏风险,这会减少后续移植的机会并增加等待时间。然而,其他因素,如供体年龄、供体类型和免疫抑制方案,会影响配型带来的益处。此外,并非所有患者都能找到完全匹配的供体,而且这通常会延长等待时间。对于没有完全匹配供体的患者,优化移植的策略应考虑不同不匹配所代表的免疫屏障:考虑患者的HLA表型,哪些是免疫原性最低的不匹配;是否应避免重复不匹配;患者是否对HLA致敏,如果是,患者抗体的强度如何?这些信息随后可用于确定免疫最佳供体的HLA类型以及出现这种供体的概率。如果概率被认为过低,可能需要通过配对捐赠扩大供体群体或修改可接受的标准,这可能需要采用治疗方法来克服免疫屏障,如增加免疫抑制或脱敏。因此,移植必须在等待最佳供体的风险与接受不太理想供体的风险之间取得平衡。