Santos T D, Macedo M D, Menegati S F P, Gilli S, Castilho L
Hemocentro Campinas-UNICAMP, Campinas, São Paulo, Brazil.
Transfus Med. 2019 Dec;29(6):423-429. doi: 10.1111/tme.12641. Epub 2019 Oct 20.
The aim of this study was to verify the possibility of performing prophylactic Rh genotype-matching in Brazilian patients with sickle cell disease (SCD) and identify the genotypes that are lacking or insufficient in our donor cohort.
Rh alloimmunisation is still a challenge in transfused patients with SCD. Rh genotype-matching may mitigate Rh alloimmunisation.
METHODS/MATERIALS: We examined the transfusion requests for antigen-matched donor units in SCD patients with Rh variants and compared the Rh altered alleles in the patients to the Rh allele frequency in a selected donor population. For each patient and donor, RBC antigen genotyping was performed using HEA, RHD and RHCE BeadChip arrays. Sequencing was used to clarify inconclusive results. Twenty-one patients and 956 Brazilian blood donors were genotyped.
According to our matching strategies, 47·6% of patients filled most of their unit requests, but 52·4% of patients had insufficient donors to fill their annual transfusion needs. We found different combinations of RHCE variant alleles in patients and donors, but the most frequent genotypes that are lacking or insufficient in our donor cohort are those associated with the lack of hr and hr high prevalence antigens and those co-inherited with altered RHD alleles.
Our study shows that the provision of compatible blood with Rh genotype-matching in Brazilian patients with SCD can be feasible but challenging and, efficient strategies of recruitment of African-Brazilian donors must be developed.
本研究旨在验证在巴西镰状细胞病(SCD)患者中进行预防性Rh基因型匹配的可能性,并确定我们的供者队列中缺乏或不足的基因型。
Rh同种免疫在接受输血的SCD患者中仍然是一个挑战。Rh基因型匹配可能会减轻Rh同种免疫。
方法/材料:我们检查了患有Rh变异的SCD患者对抗原匹配供者单位的输血需求,并将患者中Rh改变的等位基因与选定供者群体中的Rh等位基因频率进行了比较。对于每位患者和供者,使用HEA、RHD和RHCE BeadChip芯片进行红细胞抗原基因分型。测序用于澄清不确定的结果。对21名患者和956名巴西献血者进行了基因分型。
根据我们的匹配策略,47.6%的患者大部分单位需求得到满足,但52.4%的患者没有足够的供者来满足其年度输血需求。我们在患者和供者中发现了RHCE变异等位基因的不同组合,但我们的供者队列中缺乏或不足的最常见基因型是那些与缺乏hr和hr高流行抗原相关的基因型,以及那些与改变的RHD等位基因共同遗传的基因型。
我们的研究表明,在巴西SCD患者中提供与Rh基因型匹配的相容性血液是可行的,但具有挑战性,必须制定招募非洲裔巴西供者的有效策略。