Department of Internal Medicine, Erasmus Medical Center Transplant Institute, University Medical Center, Rotterdam, the Netherlands.
Department of Immunology, Leiden University Medical Center, Leiden, the Netherlands.
Transplantation. 2024 Feb 1;108(2):335-345. doi: 10.1097/TP.0000000000004689. Epub 2024 Jan 19.
Imlifidase, derived from a Streptococcus pyogenes enzyme, cleaves the entire immunoglobulin G pool within hours after administration in fully cleaved antigen-binding and crystallizable fragments. These cleaved fragments can no longer exert their antibody-dependent cytotoxic functions, thereby creating a window to permit HLA-incompatible kidney transplantation. Imlifidase is labeled, in Europe only, for deceased donor kidney transplantation in highly sensitized patients, whose chances for an HLA-compatible transplant are negligible. This review discusses outcomes of preclinical and clinical studies on imlifidase and describes the phase III desensitization trials that are currently enrolling patients. A comparison is made with other desensitization methods. The review discusses the immunological work-up of imlifidase candidates and especially the "delisting strategy" of antigens that shift from unacceptable to acceptable with imlifidase desensitization. Other considerations for clinical implementation, such as adaptation of induction protocols, are also discussed. Imlifidase cleaves most of the currently used induction agents except for horse antithymocyte globulin, and rebound of donor-specific antibodies should be managed. Another consideration is the timing and interpretation of (virtual) crossmatches when bringing this novel desensitization agent into the clinic.
依库珠单抗源自酿脓链球菌酶,在给药后数小时内即可将整个免疫球蛋白 G 池完全裂解为抗原结合和可结晶片段。这些裂解片段将无法再发挥其抗体依赖的细胞毒性功能,从而为 HLA 不相容的肾脏移植创造了一个窗口期。依库珠单抗仅在欧洲被批准用于高度致敏患者的已故供体肾脏移植,这些患者 HLA 匹配移植的机会微乎其微。本文讨论了依库珠单抗的临床前和临床研究结果,并描述了目前正在招募患者的 III 期脱敏试验。此外,还与其他脱敏方法进行了比较。本文讨论了依库珠单抗候选物的免疫学检查,特别是依库珠单抗脱敏时将抗原从不可接受变为可接受的“除名策略”。还讨论了临床实施的其他注意事项,例如诱导方案的调整。依库珠单抗可裂解目前使用的大多数诱导剂,除了马抗胸腺细胞球蛋白,而供体特异性抗体的反弹应加以管理。另一个需要考虑的因素是在将这种新型脱敏剂引入临床时,时机和(虚拟)交叉配型的解读。