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Immunoglobulin G to virus-specific early antigens in congenital primary and reactivated human cytomegalovirus infections.

机译:对先天性原发性和再活化的人巨细胞病毒感染中病毒特异性早期抗原的免疫球蛋白G。

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摘要

Immunoglobulin G antibody to human cytomegalovirus (CMV)-specific early antigens (EA-Ab) was determined by the immunoperoxidase antibody technique in several cases of congenital, primary, and reactivated CMV infections. Mothers of congenitally infected infants and a group of leukemic children and pregnant women were also studied. In 11 cases of congenital infection, CMV EA-Ab was always associated with CMV excretion whether immunoglobulin M antibody was present or not. Nine mothers of congenitally infected infants had CMV EA-Ab for several months after delivery, but association with CMV elimination was not established when urine and/or saliva were tested for virus isolation. In all nine cases of primary CMV infection, CMV EA-Ab was present, and in five its detection was associated with CMV isolation. In one case, disappearance of EA-Ab occurred when virus excretion ceased. In five cases of reactivated CMV infections, a consistent association between CMV EA-Ab and virus isolation was found. Six of 31 leukemia children had CMV EA-Ab, and virus was isolated from 3 of these. Four of 28 pregnant women showed EA-Ab in their serum, but tests for isolation were not done. These data suggest that CMV EA-Ab is not a marker of a current primary CMV infection, as previously reported, but a marker of an active CMV replication which can take place in primary as well as in congenital and reactivated CMV infections.
机译:在几种先天性,原发性和再活化的CMV感染病例中,通过免疫过氧化物酶抗体技术确定了针对人巨细胞病毒(CMV)特异性早期抗原(EA-Ab)的免疫球蛋白G抗体。还对先天感染婴儿的母亲以及一群白血病儿童和孕妇进行了研究。在11例先天性感染病例中,无论是否存在免疫球蛋白M抗体,CMV EA-Ab总是与CMV排泄相关。 9名先天性感染婴儿的母亲在分娩后数月内接受了CMV EA-Ab的治疗,但是当对尿液和/或唾液进行病毒分离测试时,并未发现与CMV消除相关。在所有9例原发性CMV感染病例中,均存在CMV EA-Ab,其中5例其检测与CMV分离有关。在一种情况下,病毒排泄停止后,EA-Ab消失。在5例重新激活的CMV感染病例中,发现了CMV EA-Ab与病毒分离之间的一致性。 31名白血病儿童中有6名患有CMV EA-Ab,并从其中3名中分离出病毒。 28名孕妇中有4名在血清中显示EA-Ab,但未进行分离测试。这些数据表明,如先前报道的那样,CMV EA-Ab不是当前原发性CMV感染的标志物,而是可以在原发性以及先天性和再活化的CMV感染中发生的有效CMV复制的标志物。

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