血清学
表位
医学
输血
抗原
免疫学
血型(非人类)
红细胞
表型
同种抗体
免疫
抗体
生物
ABO血型系统
遗传学
基因
作者
Yanli Ji,Yalin Luo,Jizhi Wen,Yuanfan Sun,Shuangshuang Jia,Chun‐Quan Ou,Wen‐Bin Yang,Jingwang Chen,Han-shen Ye,Xiangfu Liu,Yong-Neng Liang,Zhigang Lu,Ying Feng,Xinzhong Wu,Muzhou Xiao,Jian-kun Mo,Zhenhai Zhou,Zhen Wang,Liao Zhijian,Jun‐Hu Chen
出处
期刊:Blood
[Elsevier BV]
日期:2023-01-13
被引量:17
标识
DOI:10.1182/blood.2022018152
摘要
Red blood cells (RBCs) of Asian-type DEL phenotype express few RhD proteins and are typed as serologic RhD-negative (D-) phenotype in routine testing. RhD-positive (D+) RBC transfusion for patients with Asian-type DEL has been proposed but has not been generally adopted because of a lack of direct evidence regarding its safety and the underlying mechanism. We performed a single-arm multicenter clinical trial to document the outcome of D+ RBC transfusion in patients with Asian-type DEL; 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 4045 serologic D- pregnant women throughout China; alloanti-D was found only in individuals with true D- (2.63%, 79/3009), but not in those with Asian-type DEL (0/1032). 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 after transfusion or pregnancy. Therefore, we recommend considering D+ RBC transfusion and discontinuing anti-D prophylaxis in patients with Asian-type DEL, including pregnant women. This clinical trial is registered at www.clinicaltrials.gov as #NCT03727230.
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