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采用体外检测法检测尖锐湿疣和宫颈发育异常患者中针对HPV-11的血清学中和抗体。

Detection of serologic neutralizing antibodies against HPV-11 in patients with condyloma acuminata and cervical dysplasia using an in vitro assay.

作者信息

Leiserowitz G S, Hall K S, Foster C A, Hitchcock M E, Christensen N D, Heim K, Smith L H

机构信息

Department of Obstetrics and Gynecology, University of California, Davis Medical Center, Sacramento 95818, USA.

出版信息

Gynecol Oncol. 1997 Aug;66(2):295-9. doi: 10.1006/gyno.1997.4743.

Abstract

This study was designed to investigate if neutralizing antibodies against HPV-11 are detectable in the serum of patients with condyloma acuminata (CA) or cervical intraepithelial neoplasia (CIN) using an in vitro infectivity assay for HPV-11. Purified HPV-11 virions were extracted from xenografted condyloma tissues implanted into athymic mice and used to infect cultured neonatal human foreskin keratinocytes (HFK) and an immortalized adult skin cell line (HaCaT). The presence of HPV-11-specific E1--E4 mRNA as detected by reverse transcriptase-polymerase chain reaction was indicative of early infection. Sera previously characterized for reactivity to HPV-11 and HPV-11 VLP (virus-like particles) by ELISA were tested for the ability to prevent HPV-11 in vitro infectivity. Neutralizing antibodies against HPV-11 were demonstrated when monoclonal antibodies or patient serum preincubated with HPV-11 virions prevented the infection of either of the two cell cultures, as shown by the absence of the E1--E4 mRNA transcript. Eleven (of 20) patients with CA were strongly ELISA reactive against HPV-11 virus-like particles. Five of these 11 patients also had detectable levels of neutralizing antibodies in their serum. It was also demonstrated that the neutralizing properties of the serum were titratable by endpoint dilution. None of 15 patients with CIN had detectable neutralizing antibodies against HPV-11. Neutralizing antibodies against HPV-11 can be detected in some patients with CA and the neutralizing effects of the patient sera can be titrated by endpoint dilution. The in vitro assay for the detection of neutralizing antibodies against HPV-11 may have utility for investigating the natural history of HPV infection and resolution, as well as assessing the efficacy of any putative HPV vaccine.

摘要

本研究旨在通过一种针对人乳头瘤病毒11型(HPV-11)的体外感染性检测方法,调查尖锐湿疣(CA)或宫颈上皮内瘤变(CIN)患者血清中是否能检测到抗HPV-11的中和抗体。从植入无胸腺小鼠的异种移植尖锐湿疣组织中提取纯化的HPV-11病毒粒子,用于感染培养的新生儿人包皮角质形成细胞(HFK)和永生化成人皮肤细胞系(HaCaT)。通过逆转录聚合酶链反应检测到HPV-11特异性E1-E4 mRNA的存在表明早期感染。通过酶联免疫吸附测定(ELISA)先前已鉴定出对HPV-11和HPV-11病毒样颗粒(VLP)有反应性的血清,检测其预防HPV-11体外感染的能力。当与HPV-11病毒粒子预孵育的单克隆抗体或患者血清可预防两种细胞培养物中的任何一种被感染时,即表明存在抗HPV-11的中和抗体,这可通过E1-E4 mRNA转录本的缺失来证明。20例CA患者中有11例对HPV-11病毒样颗粒有强烈的ELISA反应性。这11例患者中有5例血清中也可检测到中和抗体水平。还证明血清的中和特性可通过终点稀释法进行滴定。15例CIN患者中无一例检测到抗HPV-11的中和抗体。在一些CA患者中可检测到抗HPV-11的中和抗体,并且患者血清的中和作用可通过终点稀释法进行滴定。用于检测抗HPV-11中和抗体的体外检测方法可能有助于研究HPV感染和清除的自然史,以及评估任何假定的HPV疫苗的疗效。

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