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采用四种不同方法对弱D与弱反应性D进行血清学比较。

Serological comparison of weak D versus weakly reacting D by four different methods.

作者信息

Sahoo Dibyajyoti, Kanungo Girija Nandini, Behera Rachita, Jena Partha Sarathi

机构信息

Department of Transfusion Medicine, JIPMER Blood Centre, JIPMER, Puducherry, India.

Department of Transfusion Medicine, Institute of Medical Sciences and SUM Hospital, Bhubaneswar, Odisha, India.

出版信息

Asian J Transfus Sci. 2024 Jul-Dec;18(2):277-280. doi: 10.4103/ajts.AJTS_34_21. Epub 2022 Sep 28.

Abstract

INTRODUCTION

Weak D red cells were defined as having a reduced amount of D antigen (formerly called "Du") that required an indirect antiglobulin test (IAT) for detection. Weakly reacting D is those which give <2+ reactions on routine methods. The present study is sharing our experience on weak D and weakly positive anti-D in various methods.

MATERIALS AND METHODS

All the blood sample of patients and blood donor, which were RhD negative, were included in the study. Furthermore, RhD positive sample <2+ was included. We repeated blood grouping of all these samples by gel card (Tulip), tube method (two different antisera), slide method, and Solid Phase Red Cell Adherence (SPRCA) (Immucore, USA).

RESULTS

A total number of samples were 27,245. RhD negative found out to be 945 (3.46%). Out of all, 929 (98.3%) samples were Rh D negative in gel card and IAT negative, while 16 (1.7%) were weak D positive. Rh D typing with these samples by different antisera at four platforms showed that 14 were weakly positive (<2+) in any of the four platforms. Similarly, out of 26,300 Rh D Positive samples, 21 samples (0.079%) were serologically weak (<2+). Repeat Rh D typing was done with different antisera in all four platforms. Result showed more than 50% were Rh D negative in any of four platforms.

CONCLUSION

Above observation showed that serological tests at various platforms failed to distinguish weak D from weakly reacting D. Thus, we propose that weakly reacting D should be treated equal as weak D unless they are distinguished by genotyping.

摘要

引言

弱D红细胞被定义为D抗原量减少(以前称为“Du”),需要通过间接抗球蛋白试验(IAT)进行检测。弱反应性D是指在常规方法中反应强度<2+的情况。本研究分享了我们在多种方法中检测弱D和弱阳性抗-D的经验。

材料与方法

本研究纳入了所有RhD阴性的患者和献血者血液样本。此外,还纳入了反应强度<2+的RhD阳性样本。我们通过凝胶卡(Tulip)、试管法(两种不同抗血清)、玻片法和固相红细胞黏附试验(SPRCA)(美国Immucore公司)对所有这些样本进行血型复检。

结果

样本总数为27245份。其中RhD阴性样本有945份(3.46%)。在所有样本中,凝胶卡检测显示929份(98.3%)样本RhD阴性且IAT阴性,而16份(1.7%)为弱D阳性。在四个平台上使用不同抗血清对这些样本进行RhD分型检测发现,在四个平台中的任何一个平台上有14份样本呈弱阳性(<2+)。同样,在26300份RhD阳性样本中,有21份样本(0.079%)血清学反应较弱(<2+)。在所有四个平台上使用不同抗血清对这些样本进行RhD分型复检。结果显示,在四个平台中的任何一个平台上,超过50%的样本RhD阴性。

结论

上述观察结果表明,不同平台的血清学检测无法区分弱D和弱反应性D。因此,我们建议,除非通过基因分型进行区分,否则弱反应性D应与弱D同等对待。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25f9/11734792/9e23f174330b/AJTS-18-277-g001.jpg

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