Saris Anno, Pavenski Katerina
Department of Infectious Diseases, Leiden University Medical Centre, Leiden, the Netherlands.
Departments of Medicine and Laboratory Medicine, St. Michael's Hospital and University of Toronto, Toronto, Ontario, Canada.
Transfus Med Rev. 2020 Oct;34(4):250-257. doi: 10.1016/j.tmrv.2020.09.010. Epub 2020 Oct 7.
Despite significant advancements in the production of platelet products, storage, and transfusion, transfusion refractoriness remains a significant clinical problem, affecting up to 14% of hematological patients receiving platelet transfusions. Human leukocyte antigen (HLA) alloimmunization is a major cause of immune platelet refractoriness, and its rate can be significantly reduced by implementation of leukoreduction. Despite promising preclinical results, pathogen reduction does not reduce HLA alloimmunization. Patients with HLA alloimmune refractoriness are usually managed with HLA-selected platelet transfusions. In this review, we describe the pathophysiology of HLA alloimmunization and alloimmune refractoriness, as well as options to prevent and treat these transfusion complications. We discuss the evidence supporting these options and point out the outstanding gaps. Finally, we review the possible future directions for prevention and treatment of alloimmune refractoriness.
尽管在血小板制品的生产、储存和输血方面取得了重大进展,但输血难治性仍然是一个重大的临床问题,影响着高达14%接受血小板输血的血液学患者。人类白细胞抗原(HLA)同种免疫是免疫性血小板难治性的主要原因,通过实施白细胞滤除可显著降低其发生率。尽管临床前结果令人鼓舞,但病原体灭活并不能降低HLA同种免疫。HLA同种免疫难治性患者通常采用HLA配型选择的血小板输血进行治疗。在本综述中,我们描述了HLA同种免疫和同种免疫难治性的病理生理学,以及预防和治疗这些输血并发症的方法。我们讨论了支持这些方法的证据,并指出了存在的显著差距。最后,我们回顾了预防和治疗同种免疫难治性的可能未来方向。