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基德系统抗原表达的暂时抑制伴随着抗Jk3的短暂产生。

Temporary suppression of Kidd system antigen expression accompanied by transient production of anti-Jk3.

作者信息

Issitt P D, Obarski G, Hartnett P L, Wren M R, Prewitt P L

机构信息

American Red Cross Blood Services, South Florida Region, Miami.

出版信息

Transfusion. 1990 Jan;30(1):46-50. doi: 10.1046/j.1537-2995.1990.30190117630.x.

Abstract

This report describes an 85-year-old woman of Russian Jewish extraction whose red cell Kidd system phenotype changed during the 2 years in which her blood was studied. Certainly once, and perhaps twice, the patient's phenotype changed from Jk(a+b-) to Jk(a-b-). On both occasions, it reverted to Jk(a+b-). During the first episode of loss of Jka, she formed anti-Jk3. Although this antibody was weak, it was capable of in vivo destruction of Jk(a+b-) and Jk(a-b+) red cells. A lack of details about the patient's clinical condition precludes speculation as to the cause of suppression of Jka expression. The phenomenon appeared to affect only the Kidd blood group system. This case should alert others that antigen loss can occur in the Kidd system as it has been shown to occur in, at least, the Rh, Kell, and Ge systems.

摘要

本报告描述了一位85岁的俄罗斯犹太裔女性,在对其血液进行研究的2年期间,她的红细胞基德系统表型发生了变化。该患者的表型确实有一次,或许还有两次,从Jk(a+b-)转变为Jk(a-b-)。在这两种情况下,又都恢复为Jk(a+b-)。在首次Jka缺失期间,她产生了抗Jk3。尽管这种抗体较弱,但它能够在体内破坏Jk(a+b-)和Jk(a-b+)红细胞。由于缺乏该患者临床状况的详细信息,无法推测Jka表达受抑制的原因。这种现象似乎仅影响基德血型系统。该病例应提醒其他人,基德系统中可能会出现抗原丢失,正如在至少Rh、凯尔和杰系统中已被证明会出现的那样。

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