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Patients with Asian-type DEL can safely be transfused using RhD-positive blood
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 regardi...
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Published in: | Blood 2023-01, Vol.191 (2), p.445-458 |
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creator | Ji, Yanli Luo, Yalin Wen, Jizhi Sun, Yuanfan Jia, Shuangshuang Ou, Chunquan Yang, Wenbing Chen, Jingwang Ye, Hanshen Liu, Xiangfu Liang, Yongneng Lu, Zhigang Feng, Ying Wu, Xinzhong Xiao, Muzhou Mo, Jiankun Zhou, Zhenhai Wang, Zhen Liao, Zhijian Chen, Junhu Wei, Ling Luo, Guangping Santoso, Sentot Fichou, Yann Flegel, Willy A Shao, Chaopeng Li, Chengyao Zhang, Rui Fu, Yongshui |
description | 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. |
doi_str_mv | 10.1182/blood.2022018152 |
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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.</description><identifier>ISSN: 0006-4971</identifier><identifier>EISSN: 1528-0020</identifier><identifier>DOI: 10.1182/blood.2022018152</identifier><identifier>PMID: 36638337</identifier><language>eng</language><publisher>American Society of Hematology</publisher><subject>Life Sciences</subject><ispartof>Blood, 2023-01, Vol.191 (2), p.445-458</ispartof><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c1642-4b3920a445bd24df41272f0d20133c878e789ef89ba79db1cdd414dc62eb16d63</citedby><orcidid>0000-0003-0886-2193 ; 0000-0001-6943-3945 ; 0000-0002-0092-8576 ; 0000-0002-5104-9125 ; 0000-0002-2147-5086 ; 0000-0001-6792-5612 ; 0000-0001-6866-7213 ; 0000-0001-9000-5021</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://hal.science/hal-04188122$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Ji, Yanli</creatorcontrib><creatorcontrib>Luo, Yalin</creatorcontrib><creatorcontrib>Wen, Jizhi</creatorcontrib><creatorcontrib>Sun, Yuanfan</creatorcontrib><creatorcontrib>Jia, Shuangshuang</creatorcontrib><creatorcontrib>Ou, Chunquan</creatorcontrib><creatorcontrib>Yang, Wenbing</creatorcontrib><creatorcontrib>Chen, Jingwang</creatorcontrib><creatorcontrib>Ye, Hanshen</creatorcontrib><creatorcontrib>Liu, Xiangfu</creatorcontrib><creatorcontrib>Liang, Yongneng</creatorcontrib><creatorcontrib>Lu, Zhigang</creatorcontrib><creatorcontrib>Feng, Ying</creatorcontrib><creatorcontrib>Wu, Xinzhong</creatorcontrib><creatorcontrib>Xiao, Muzhou</creatorcontrib><creatorcontrib>Mo, Jiankun</creatorcontrib><creatorcontrib>Zhou, Zhenhai</creatorcontrib><creatorcontrib>Wang, Zhen</creatorcontrib><creatorcontrib>Liao, Zhijian</creatorcontrib><creatorcontrib>Chen, Junhu</creatorcontrib><creatorcontrib>Wei, Ling</creatorcontrib><creatorcontrib>Luo, Guangping</creatorcontrib><creatorcontrib>Santoso, Sentot</creatorcontrib><creatorcontrib>Fichou, Yann</creatorcontrib><creatorcontrib>Flegel, Willy A</creatorcontrib><creatorcontrib>Shao, Chaopeng</creatorcontrib><creatorcontrib>Li, Chengyao</creatorcontrib><creatorcontrib>Zhang, Rui</creatorcontrib><creatorcontrib>Fu, Yongshui</creatorcontrib><title>Patients with Asian-type DEL can safely be transfused using RhD-positive blood</title><title>Blood</title><description>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. 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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. 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title | Patients with Asian-type DEL can safely be transfused using RhD-positive blood |
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