研究弱2型D基因型个体的抗D抗体。

Q4 Medicine Immunohematology Pub Date : 2022-09-22 Print Date: 2022-09-01 DOI:10.21307/immunohematology-2022-046
S Phou, N Nguyen, J Revilla, K Rodberg, D R Gibb, S H Pepkowitz, E B Klapper
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引用次数: 0

摘要

弱D表型个体的抗D是一个意外的发现,可能需要进一步的调查来确定抗D是自身抗体还是同种抗体。进一步的调查可能还包括评估患者的RHD基因型和排除抗- g。我们报告了一例84岁的弱D 2型基因型男性,他在抗c的同时出现了一种意想不到的抗D。尽管同种异体抗-D和自身抗-D之间的区别可能难以确定,但具有弱D 2型基因型的个体被认为没有发生同种异体抗-D的风险。此外,调查可能会影响输血建议。尽管抗- d的临床意义尚不确定,但该患者仅限于交叉配伍的D-C-红细胞。本报告是少数报告的具有弱D 2型基因型的个体具有可证实的抗D,但没有同种异体抗D的证据的病例之一。
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Investigating anti-D in an individual with the weak D type 2 genotype.

Anti-D in individuals with a weak D phenotype is an unexpected finding that may require additional investigation to determine whether the anti-D is an autoantibody or alloantibody. Further investigation may also include assessment of the patient's RHD genotype and exclusion of anti-G. We present a case of an 84-year-old man with the weak D type 2 genotype who developed an unexpected anti-D along with anti-C. Individuals with the weak D type 2 genotype are thought not to be at risk for developing alloanti-D, although the distinction between alloanti-D and autoanti-D may be difficult to ascertain. Furthermore, investigations may affect transfusion recommendations. This patient was restricted to crossmatch-compatible, D-C- red blood cells even though the clinical significance of the anti-D was uncertain. This report is one of a few reported cases of an individual with the weak D type 2 genotype with demonstrable anti-D but without evidence for alloanti-D.

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来源期刊
Immunohematology
Immunohematology Medicine-Medicine (all)
CiteScore
1.30
自引率
0.00%
发文量
18
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