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Patients with Asian-type DEL can safely be transfused using RhD-positive blood.

Yanli JiYalin LuoJizhi WenYuanfan SunShuangshuang JiaChun-Quan OuWenbing YangJingwang ChenHanshen YeXiangfu LiuYongneng LiangZhigang LuYing FengXinzhong WuMuzhou XiaoJiankun MoZhenhai ZhouZhen WangZhijian LiaoJunhu ChenLing WeiGuangping LuoSentot SantosoYann FichouWilly Albert FlegelChaopeng ShaoChengyao LiRui ZhangYongshui Fu
Published in: Blood (2023)
Red blood cells (RBCs) of the Asian-type DEL phenotype express few RhD proteins and are typed as serologic RhD-negative (D-) in routine testing. RhD-positive (D+) RBC transfusion for Asian-type DEL patients has been proposed but has not been generally adopted due to a lack of direct evidence regarding its safety and underlying mechanism. We performed a single-arm multicenter clinical trial to document the outcome of D+ RBC transfusion in Asian-type DEL patients; none of the recipients (0/42; 95% confidence interval, 0%-8.40%) developed alloanti-D after a median follow-up of 226 days. We conducted a large retrospective study to detect alloanti-D immunization in 4,045 serologic D- pregnant women throughout China; alloanti-D was found only in true D- individuals (2.63%, 79/3,009), but not in those with Asian-type DEL (0/1,032). We further retrospectively examined 127 serologic D- pregnant women who had developed alloanti-D and found none with Asian-type DEL (0/127). Finally, we analyzed RHD transcripts from Asian-type DEL erythroblasts and examined antigen epitopes expressed by various RHD transcripts in vitro, finding a low abundance of full-length RHD transcripts (0.18% of the total) expressing RhD antigens carrying the entire repertoire of epitopes, which could explain the immune tolerance against D+ RBCs. Our results provide multiple lines of evidence that individuals with Asian-type DEL cannot produce alloanti-D when exposed to D+ RBCs following transfusion or pregnancy. Therefore, we recommend considering D+ RBC transfusion and discontinuing anti-D prophylaxis in Asian-type DEL patients, including pregnant women. This clinical trial is registered at www.clinicaltrials.gov as NCT03727230.
Keyphrases
  • pregnant women
  • clinical trial
  • end stage renal disease
  • chronic kidney disease
  • ejection fraction
  • red blood cell
  • newly diagnosed
  • cardiac surgery
  • prognostic factors
  • sars cov
  • pregnancy outcomes
  • cross sectional