雅温得大学和医院中心血液制品供者和受者的ABO、RH和Kell血型系统的红细胞表型

B. C. Chemegni, A. Ndoumba, Jiatsa Bogning, E. Lontsi, CB Tayou Tagne, D. Mbanya
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引用次数: 0

摘要

为了防止输血后同种异体免疫,必须向受者提供相容的血液制品。然而,在收入有限的国家,血型仅限于ABO系统和恒河猴系统的D抗原;然而,还有其他免疫原性抗原,如C、C、E、E和K等。这应该就是为什么2009年,Tayou等人在雅温市大学医院中心血库对供血者和受血者的红细胞表型进行回顾性研究时,只向我们报告了红细胞血型系统ABO和Rh 1抗原的数据。因此,我们发现在雅温德医院血液制品供者和受者的ABO、RH和KELL血型系统中进行红细胞表型分析是有利的。本研究于2017年6月1日至2017年12月31日6个多月的时间内,在雅温得市CHU血库进行了一项描述性、横向、前瞻性研究。它对捐赠者的原创研究文章Chemegni等人感兴趣;国际生物医学杂志,11(1):31-37,2020;文章no.IBRR。56051 32对受血人,其中受血人是在保健所住院的病人。供体和受体血液样本的实验室分析使我们能够在ABO, RH和KELL血型系统中获得表型。在ABO系统中,获得的表型为4种:A1、A1B、B和O,供者分别占27.27%、2.27%、13.64%和56.82%,受体占31.82%、2.27%、13.64%和52.27%。此外,从恒河系统,捐赠者有5表型:D + C + E + E C + +,英汉+ E D + C + +, D +汉英+ C + E + D + CE-c + E + DCE-c + E +分别为2.27%,11.36%,9.09%,75.00%和2.27%,而接受者4表型,即:D + C + E + E C + +, D +汉英+ C + E + D + CE-c + E + DCE-c + E + 15.91%,分别为27.27%、54.55%和2.27%。在KELL系统中,4.55%的供体和2.27%的受体存在K抗原。从供体到受体的抗原供给率分别为C的6.82%、E的4.54%、K的2.27%和K、C、E的2.27%。这使我们估计同种异体免疫的平均风险为15.9%。因此,红细胞表型在输血过程中具有重要的益处,并可大大预防同种异体免疫的风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Erythrocyte Phenotyping in ABO, RH and Kell Blood Group Systems in the Donor and Recipient of Blood Products at the Yaounde University and Hospital Center
In order to prevent post transfusion alloimmunization, it is essential to give recipients compatible blood products. However in countries with limited income, blood grouping is limited to the ABO system and to the D antigen of the Rhesus system; however, there are other immunogenic antigens such as C, c, E, e and K to name a few. This should be the reason why a retrospective study by Tayou et al. at the blood bank of the University Hospital Center (CHU) of Yaoundé in 2009 on the erythrocyte phenotype in the donor and recipient of blood product only reported to us that data relate to the erythrocyte blood group system ABO and the Rh 1 antigen. We therefore found it expedient to carry out erythrocyte phenotyping in the ABO, RH and KELL blood group systems in the donor and recipient of blood products at the CHU of Yaoundé. A descriptive, transversal and prospective study was carried out at the blood bank of the CHU of Yaoundé over 6 months, from June 1, 2017 to December 31, 2017. It was interested in the donorOriginal Research Article Chemegni et al.; IBRR, 11(1): 31-37, 2020; Article no.IBRR.56051 32 recipient couples of blood within which the recipient was a patient hospitalized at the CHU. Laboratory analyses of donor and recipient blood samples have allowed us to have the phenotypes in the ABO, RH, and KELL blood group systems. In the ABO system, the phenotypes obtained were 4: A1, A1B, B and O at 27.27%, 2.27%, 13.64% and 56.82% respectively among donors and 31.82%, 2.27%, 13.64% and 52.27% among recipients. In addition, from the Rhesus system, there were 5 phenotypes in donors: D + C + E + c + e +, D + C + E-c + e +, D + C-E + c + e +, D + CE-c + e +, DCE-c + e + respectively at 2.27%, 11.36%, 9.09%, 75.00% and 2.27% and in recipients 4 phenotypes, namely: D + C + E + c + e +, D + C-E + c + e +, D + CE-c + e +, DCE-c + e + at 15.91%, 27.27%, 54.55% and 2.27% respectively. In the KELL system, the K antigen was present in 4.55% of donors and 2.27% of recipients. An antigen supply from the donor to the recipient was evaluated at 6.82% for C, 4.54% for E, 2.27% for K and 2.27% for K, C, E at the same time. This gave us an estimate of the average risk of alloimmunization at 15.9%. Erythrocyte phenotyping would therefore be of major benefit during blood transfusion and would considerably prevent the risks of alloimmunization.
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