Transfusional Medicine Group, Vall d'Hebron Research Institute, Universitat Autònoma of Barcelona (VHIR-UAB), Barcelona, Spain.
Immunogenetics and Histocompatibility Laboratory, Blood and Tissue Bank, Barcelona, Spain.
HLA. 2024 Mar;103(3):e15419. doi: 10.1111/tan.15419.
Adoptive cell therapy using virus-specific T cells (VST) is a strategy for treating common opportunistic viral infections after transplantation, particularly when these infections do not resolve through antiviral drug therapy. The availability of third-party healthy donors allows for the immediate use of cells for allogeneic therapy in cases where patients lack an appropriate donor. Here, we present the creation of a cell donor registry of human leukocyte antigen (HLA)-typed blood donors, REDOCEL, a strategic initiative to ensure the availability of compatible cells for donation when needed. Currently, the registry consists of 597 healthy donors with a median age of 29 years, 54% of whom are women. The most represented blood groups were A positive and O positive, with 36.52% and 34.51%, respectively. Also, donors were screened for cytomegalovirus (CMV) and Epstein-Barr virus (EBV). Almost 65% of donors were CMV-seropositive, while less than 5% were EBV-seronegative. Of the CMV-seropositive donors, 98% were also EBV-seropositive. High-resolution HLA-A, -B, -C, -DRB1 and -DQB1 allele and haplotype frequencies were determined in the registry. Prevalent HLA alleles and haplotypes were well represented to ensure donor-recipient HLA-matching, including alleles reported to present viral immunodominant epitopes. Since the functional establishment of REDOCEL, in May 2019, 87 effective donations have been collected, and the effective availability of donors with the first call has been greater than 75%. Thus, almost 89% of patients receiving an effective donation had available at least 5/10 HLA-matched cell donors (HLA-A, -B, -C, -DRB1, and -DQB1). To summarize, based on our experience, a cell donor registry from previously HLA-typed blood donors is a useful tool for facilitating access to VST therapy.
采用病毒特异性 T 细胞(VST)的过继细胞疗法是治疗移植后常见机会性病毒感染的一种策略,尤其是在这些感染无法通过抗病毒药物治疗解决的情况下。第三方健康供者的可用性允许在患者缺乏合适供者的情况下,立即使用细胞进行同种异体治疗。在这里,我们介绍了人类白细胞抗原(HLA)型血液供者细胞供者登记处 REDOCEL 的创建,这是一项战略举措,旨在确保在需要时可获得用于捐赠的相容细胞。目前,该登记处包含 597 名健康供者,中位年龄为 29 岁,其中 54%为女性。最常见的血型为 A 阳性和 O 阳性,分别占 36.52%和 34.51%。此外,对供者进行了巨细胞病毒(CMV)和 Epstein-Barr 病毒(EBV)的筛查。近 65%的供者为 CMV 血清阳性,而不到 5%的供者为 EBV 血清阴性。CMV 血清阳性供者中,98%也为 EBV 血清阳性。在登记处确定了高分辨率 HLA-A、-B、-C、-DRB1 和-DQB1 等位基因和单倍型频率。登记处中存在代表性良好的常见 HLA 等位基因和单倍型,以确保供者与受者 HLA 匹配,包括报告存在病毒免疫显性表位的等位基因。自 2019 年 5 月 REDOCEL 功能建立以来,已采集了 87 次有效捐赠,首次调用时有效供者的可用性大于 75%。因此,接受有效捐赠的患者中,几乎 89%至少有 5/10 HLA 匹配的细胞供者(HLA-A、-B、-C、-DRB1 和-DQB1)可用。总之,根据我们的经验,来自先前 HLA 分型血液供者的细胞供者登记处是促进 VST 治疗的有用工具。