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首页> 外文期刊>The Journal of Infectious Diseases >Delayed generation of antibodies mediating human immunodeficiency virus type 1-specific antibody-dependent cellular cytotoxicity in vertically infected infants. WITS Study Group. Women and Infants Transmission Study.
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Delayed generation of antibodies mediating human immunodeficiency virus type 1-specific antibody-dependent cellular cytotoxicity in vertically infected infants. WITS Study Group. Women and Infants Transmission Study.

机译:在垂直感染的婴儿中,介导人类免疫缺陷病毒1型特异性抗体依赖性细胞毒性的抗体的产生延迟。 WITS研究小组。妇女和婴儿传播研究。

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摘要

Human immunodeficiency virus type 1 (HIV-1)-specific antibody-dependent cellular cytotoxicity (ADCC) antibody titers were serially measured from birth to 24 months in the plasma of 14 intrapartum-infected and 10 uninfected infants born to HIV-1-infected women. The mean ADCC antibody titers measured at birth in infected and uninfected infants were similar (10(-3.9) and 10(-4.0), respectively), suggesting that ADCC antibodies did not protect infants from the intrapartum transmission of HIV-1. In infected infants, ADCC titers at birth did not predict subsequent clinical disease course. The active production of HIV-1-specific ADCC antibodies was detected in most infected infants only after 12 months of age, well after the loss of passively acquired maternal ADCC antibody. The delayed production of ADCC antibodies in infancy may account, in part, for the less efficient control of viral replication and more rapid disease progression following vertical infection compared with that in adults.
机译:从出生至24个月期间,对14名受HIV-1感染的妇女出生的14例感染和10例未感染的婴儿的血浆中从出生至24个月连续测量了人类免疫缺陷病毒1型(HIV-1)特异性抗体依赖性细胞毒性(ADCC)抗体滴度。在感染和未感染的婴儿出生时测得的ADCC抗体平均滴度相似(分别为10(-3.9)和10(-4.0)),这表明ADCC抗体不能保护婴儿免受HIV-1的分娩传播。在受感染的婴儿中,出生时的ADCC滴度无法预测随后的临床疾病进程。在大多数感染婴儿中,只有在失去被动获得的母体ADCC抗体后,才在12个月大时检测到HIV-1特异性ADCC抗体的活跃产生。与成人相比,婴儿期ADCC抗体生产延迟可能部分解释了病毒复制的控制效率较低,垂直感染后疾病进展更快。

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