首页> 美国卫生研究院文献>Clinical and Diagnostic Laboratory Immunology >Mother-Infant Transfer of Anti-Human Papillomavirus (HPV) Antibodies following Vaccination with the Quadrivalent HPV (Type 6/11/16/18) Virus-Like Particle Vaccine
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Mother-Infant Transfer of Anti-Human Papillomavirus (HPV) Antibodies following Vaccination with the Quadrivalent HPV (Type 6/11/16/18) Virus-Like Particle Vaccine

机译:接种四价HPV(类型6/11/16/18)病毒样颗粒疫苗后抗人乳头瘤病毒(HPV)抗体的母婴转移

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摘要

The exploratory immunogenicity objective of this analysis was to characterize the titer of vaccine human papillomavirus (HPV)-type immunoglobulins in both peripartum maternal blood and the cord blood of infants born to women who received blinded therapy. Data were derived from a randomized, placebo-controlled, double-blind safety, immunogenicity, and efficacy study (protocol 019; ). This study enrolled 3,819 women between the ages of 24 and 45 years from 38 international study sites between 18 June 2004 and 30 April 2005. Data in the current analysis are from subjects enrolled in Philippines and Thailand. For each of HPV types 6, 11, 16, and 18, maternal anti-HPV was found in cord blood samples. Furthermore, HPV titers in cord blood samples were highly positively correlated with maternal HPV titers. Additionally, there were instances when anti-HPV antibodies were no longer detectable in maternal serum samples and yet were detected in matched cord blood samples. These results demonstrate that quadrivalent HPV (qHPV) vaccine-induced antibodies cross the placenta and could potentially provide some benefit against vaccine-type HPV infection and related diseases such as recurrent respiratory papillomatosis.
机译:该分析的探索性免疫原性目标是鉴定产妇围产期母血和接受盲法治疗的妇女所生婴儿脐带血中疫苗人乳头瘤病毒(HPV)型免疫球蛋白的滴度。数据来自随机,安慰剂对照,双盲安全性,免疫原性和功效研究(协议019;)。这项研究从2004年6月18日至2005年4月30日在38个国际研究地点招募了3,819名24至45岁的妇女。当前分析的数据来自在菲律宾和泰国招募的受试者。对于每种HPV类型6、11、16和18,在脐血样本中发现了母体抗HPV。此外,脐带血样品中的HPV滴度与母体HPV滴度高度正相关。另外,有时在孕妇血清样品中不再检测到抗HPV抗体,而在匹配的脐带血样品中却检测到了。这些结果表明,四价HPV(qHPV)疫苗诱导的抗体穿过胎盘,并可能对疫苗型HPV感染和相关疾病(如反复呼吸道乳头状瘤病)提供某些益处。

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