Odds ratios and 95% confidence intervals for seropositive tertile categorizations of HPV16 assay results at baseline and risk of incident HPV16 DNA infection.

ELISA: VLP-based direct enzyme-linked immunosorbent assay; cLIA: Competitive Luminex immunoassay; SEAP-NA: Secreted alkaline phosphatase protein neutralization assay.aCategorization cutoffs for the ELISA: Low 8–16, Medium >16–59, High >59; CLIA: Low 20–52, Medium >52–120, High >120; SEAP-NA assay: Low 25–32.63, Medium >32.63–93.07, High >93.07.bSampling-adjusted population estimates (see methods).cPreviously reported in [14].ELISA：基于病毒样颗粒（Virus-like Particle, VLP）的直接酶联免疫吸附试验；cLIA：竞争性Luminex免疫分析法（Competitive Luminex immunoassay）；SEAP-NA：分泌型碱性磷酸酶蛋白中和试验（Secreted alkaline phosphatase protein neutralization assay）。a 分类截断阈值：ELISA分级标准为低浓度组（8–16）、中浓度组（>16–59）、高浓度组（>59）；cLIA分级标准为低浓度组（20–52）、中浓度组（>52–120）、高浓度组（>120）；SEAP-NA试验分级标准为低浓度组（25–32.63）、中浓度组（>32.63–93.07）、高浓度组（>93.07）。b 经抽样调整的人群估计值（详见方法部分）。c 本内容此前已在文献[14]中报道。