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扁桃体切除标本中人类乳头瘤病毒DNA的存在情况。

Presence of human papillomavirus DNA in tonsillectomy specimens.

作者信息

Sisk Jamie, Schweinfurth John M, Wang Xiaohong T, Chong Kong

机构信息

Department of Otolaryngology, University of Mississippi Medical Center, Jackson, Mississippi, USA.

出版信息

Laryngoscope. 2006 Aug;116(8):1372-4. doi: 10.1097/01.mlg.0000225973.21736.bc.

Abstract

OBJECTIVES

The objectives of this prospective case-control study were to study the prevalence of human papillomavirus (HPV) in tonsillectomy specimens from pediatric patients without recurrent respiratory papillomatosis (RRP), and to study methods of HPV detection.

METHODS

Fifty pediatric patients without known RRP undergoing tonsillectomy for hypertrophy or recurrent tonsillitis were enrolled in the study. After tonsillectomy, a 20-mg section was subjected to DNA extraction, and DNA content and purity were confirmed with spectrophotometry. Polymerase chain reaction (PCR) was performed using consensus primer pools PGMY 09/11 targeted at the L1 region. Amplification products were detected and analyzed with standard agarose gel electrophoresis. Positive samples were then subjected to reverse line blot assay to determine virus genotype. Laryngeal papilloma specimens of 15 patients obtained during routine debulking procedures were also analyzed and served as positive controls.

RESULTS

Of 50 tonsil samples tested, two were positive for HPV DNA after PCR and gel electrophoresis. One of these samples was confirmed with typing and tested positive for HPV 11. All 15 papilloma specimens were positive for DNA of HPV types 6 and/or 11.

CONCLUSIONS

In the current study, the prevalence of HPV DNA in tonsillar tissue of patients without RRP is 2%, whereas the incidence of this disease is 2 to 4 cases per 100,000 (0.004%). These findings are significantly different (P = .005 within a 95% confidence interval) suggesting that host factors in addition to infection play a role in pathogenesis of RRP. The molecular methods described in this study are well suited for detection of HPV in tonsillar tissue.

摘要

目的

本前瞻性病例对照研究的目的是研究非复发性呼吸道乳头状瘤病(RRP)的儿科患者扁桃体切除标本中人乳头瘤病毒(HPV)的患病率,并研究HPV检测方法。

方法

50名因扁桃体肥大或复发性扁桃体炎而接受扁桃体切除术且无RRP病史的儿科患者纳入本研究。扁桃体切除术后,取20毫克组织进行DNA提取,并用分光光度法确认DNA含量和纯度。使用靶向L1区域的通用引物库PGMY 09/11进行聚合酶链反应(PCR)。扩增产物用标准琼脂糖凝胶电泳进行检测和分析。阳性样本随后进行反向线印迹分析以确定病毒基因型。对15例患者在常规肿瘤切除术中获得的喉乳头状瘤标本也进行了分析,并作为阳性对照。

结果

在检测的50份扁桃体样本中,PCR和凝胶电泳后有两份HPV DNA呈阳性。其中一份样本经分型确认,HPV 11检测呈阳性。所有15份乳头状瘤标本的HPV 6型和/或11型DNA均呈阳性。

结论

在本研究中,无RRP患者扁桃体组织中HPV DNA的患病率为2%,而该病的发病率为每10万人2至4例(0.004%)。这些发现有显著差异(95%置信区间内P = 0.005),表明除感染外,宿主因素在RRP的发病机制中也起作用。本研究中描述的分子方法非常适合检测扁桃体组织中的HPV。

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