Wright Paul A
Transplantation Laboratory, Division of Surgery, Manchester University NHS Foundation Trust, Manchester, United Kingdom.
HLA. 2020 May;95(5):435-448. doi: 10.1111/tan.13817. Epub 2020 Feb 7.
Natural killer cells preferentially target and kill malignant and virally infected cells. Both these properties present compelling clinical utility in the field of haemopoietic progenitor cell transplantation (HPCT), potentially promoting a graft vs leukaemia effect in the absence of graft vs host disease and protecting against cytomegalovirus activation. Killer Ig-like receptors (KIR) play a central role in the cytotoxic action of natural killer cells, providing opportunity for improving transplantation outcomes by prioritising potential donors with optimal characteristics. Numerous algorithms for assessing KIR gene content as part of HPCT donor selection protocols exist, but no single model has been found to be universally applicable in all transplant centres. This review summarises several of the predominant strategies in KIR assessment algorithms, discussing their basic scientific principles, clinical utility and benefits to post-transplant outcomes. Finally, the review will consider how future donor selection protocols could develop towards unifying the concepts of KIR proteomics and genetics for optimising patient care.
自然杀伤细胞优先靶向并杀死恶性细胞和病毒感染细胞。这两种特性在造血祖细胞移植(HPCT)领域都具有引人注目的临床应用价值,有可能在无移植物抗宿主病的情况下促进移植物抗白血病效应,并预防巨细胞病毒激活。杀伤细胞免疫球蛋白样受体(KIR)在自然杀伤细胞的细胞毒性作用中起核心作用,通过优先选择具有最佳特征的潜在供体,为改善移植结果提供了机会。作为HPCT供体选择方案的一部分,存在许多评估KIR基因含量的算法,但尚未发现单一模型在所有移植中心都普遍适用。本综述总结了KIR评估算法中的几种主要策略,讨论了它们的基本科学原理、临床应用价值以及对移植后结果的益处。最后,本综述将考虑未来的供体选择方案如何朝着统一KIR蛋白质组学和遗传学概念的方向发展,以优化患者护理。