Prevalence of "weak B" phenotypes and their evaluation and differentiation in healthy blood donor population in Eastern India.

IF 0.6 Q4 HEMATOLOGY Asian Journal of Transfusion Science Pub Date : 2024-07-01 Epub Date: 2023-11-07 DOI:10.4103/ajts.ajts_36_23
Sudipta Sekhar Das, Sourav Mukherjee, Sourav Chowdhury
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Abstract

Background: Examples of group B red cells that react weakly or not at all with anti-B have been described. Subgroups of B such as B3, Bx, Bm, and Bel are rare and are less frequently reported. We studied the frequency of subgroups of B in our healthy blood donor population and serologically characterized and differentiated these subgroups.

Materials and methods: The 9-year prospective study included 84,534 healthy blood donors. Initial blood grouping and antibody screening of all donor samples were performed using automated solid-phase assay. Any sample showing blood group discrepancy or weaker agglutination was subjected to further immunohematological investigations.

Results: Among 84,534 healthy donors, "B" blood group was found in 29,190 (34.53%). Weak B phenotypes were demonstrated in 9 (0.031%) B donors. Among the 9 weak B phenotypes, B3 was the most common followed by Bm. The frequency of B3, Bm, Bx, and Bel in our blood donor population was found to be 1 in 21,133, 1 in 28,178, 1 in 84,534, and 1 in 84,534, respectively. Red cell agglutination with anti-B and anti-AB varied from Wk+ to 2+ with or without mixed-field agglutination in the B3 and Bx phenotypes. Naturally occurring anti-B of immunoglobulin M type was detected in the Bx donor. Two (22.2%) of the 9 donors were found to be nonsecretor. Adsorption-elution demonstrated "B" antigen specificity in different strengths in Bm, Bx, and Bel phenotypes.

Conclusion: We conclude that differentiating weak subgroups of "B" by serological assays is possible to a great extent with technical expertise. Mistyping weak subgroups of B as "O" group may lead to reporting errors and wrong blood transfusion. Therefore, blood centers in developing countries including India should establish simple techniques to detect and differentiate weak subgroups and develop procedures to ensure safe blood transfusion and transplantation.

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印度东部健康献血者人群中“弱B”表型的流行及其评估和分化
背景:B族红细胞与抗-B反应弱或完全不反应的例子已被描述过。B的亚群如B3、Bx、Bm和Bel是罕见的,报道较少。我们研究了健康献血者人群中B亚群的频率,并对这些亚群进行了血清学表征和区分。材料和方法:这项为期9年的前瞻性研究纳入了84534名健康献血者。所有供体样本的初始血型和抗体筛选使用自动固相测定法进行。任何显示血型差异或较弱凝集的样本都要进行进一步的免疫血液学检查。结果:84534名健康献血者中,B型血29190人(34.53%)。弱B型9例(0.031%)。在9种弱B表型中,B3最为常见,其次是Bm。在我们的献血者人群中,B3、Bm、Bx和Bel的频率分别为1 / 21133、1 / 28178、1 / 84534和1 / 84534。红细胞与抗b和抗ab的凝集从Wk+到2+变化,在B3和Bx表型中有或没有混合场凝集。在Bx供体中检测到自然产生的M型免疫球蛋白抗b。9名捐赠者中2名(22.2%)为非分泌物者。吸附-洗脱在Bm、Bx和Bel表型中显示了不同强度的“B”抗原特异性。结论:我们得出的结论是,通过血清学分析在很大程度上可以通过技术专长来区分“B”的弱亚群。将B型弱亚群误打为O型可能导致报告错误和错误输血。因此,包括印度在内的发展中国家的血液中心应该建立检测和区分弱亚群的简单技术,并制定确保安全输血和移植的程序。
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来源期刊
CiteScore
0.90
自引率
0.00%
发文量
56
审稿时长
44 weeks
期刊最新文献
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