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- W8520703 abstract "A key component of clinical and epidemiologic investigation of exposure-disease associations is accurate and reliable measurement of exposure and outcome. Detection of human papillomavirus (HPV) infection is important both as an outcome of sexually transmitted disease research and natural history studies and as a critical exposure measure in the study of a variety of diseases, including cervical cancer. Measurement of current HPV infection relies on the detection of HPV DNA from tissues at the site of exposure (e.g., anogenital tract). HPV DNA detection assays have evolved over the past 15 years from assays with low sensitivity and specificity (e.g., filter in situ hybridization), to assays with increasing specificity but low sensitivity (e.g., Southern blot and dot blot hybridization, including ViraPap and Hybrid Capture Tube assays), to assays with both high sensitivity and specificity (e.g., target and signal amplification systems such as PCR and Hybrid Capture 2). No single gold standard test has emerged for the detection of HPV, although several assays have been well validated for use in the detection of the types commonly found in the genital tract. Evolution of the technology to produce virus like particles (VLPs) has helped advance the development of serologic assays to detect antibodies to the L1 capsid protein of HPV as a cumulative measure of past and some prevalent HPV infections.KeywordsCervical CancerCervical Intraepithelial NeoplasiaInvasive Cervical CancerReverse Line BlotThese keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves." @default.
- W8520703 created "2016-06-24" @default.
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- W8520703 date "2004-01-01" @default.
- W8520703 modified "2023-10-16" @default.
- W8520703 title "Chapter 5 Measurement of Exposure to Human Papillomaviruses" @default.
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- W8520703 doi "https://doi.org/10.1007/1-4020-2016-3_5" @default.
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