Viscidi R P, Kotloff K L, Clayman B, Russ K, Shapiro S, Shah K V
Eudowood Division of Infectious Diseases, Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Clin Diagn Lab Immunol. 1997 Mar;4(2):122-6. doi: 10.1128/cdli.4.2.122-126.1997.
A human papillomavirus type 16 (HPV-16) virus-like particle (VLP)-based enzyme-linked immunosorbent assay (ELISA) was used to measure serum antibody to capsid proteins in 376 sexually active college women who were also screened for the presence of genital HPVs by PCR and interviewed for demographic and behavioral risk factors for HPV infection. The seroprevalence was 46% in women with HPV-16 DNA in the genital tract. The corresponding values for women who harbored other HPV types or no HPV in the genital tract were 30 and 19%, respectively (HPV-16 group versus no-HPV group; odds ratio [OR], 3.7; 95% confidence interval [CI], 1.5 to 8.9). The antibody response was significantly higher among women with a high viral load than among those with a low viral load (median optical density value, 0.838 versus 0.137, P = 0.009). Comparable levels of seroreactivity were observed among women infected with HPV types distantly or closely related genetically to HPV-16. Seroreactivity was significantly associated with an age of 25 to 30 years (OR, 2.3; 95% CI, 1.2 to 4.4), three or more lifetime sexual partners (OR, 2.9; 95% CI, 1.1 to 10), and history of a sexually transmitted disease other than HPV (OR, 3.1; 95% CI, 1.5 to 6.3). The percent seropositivity increased linearly with number of lifetime sexual partners until reaching a plateau at 35% for women with more than six partners (chi for linear trend, P < 0.001). The low sensitivity of HPV-16 VLP-based ELISA may limit the usefulness of the assay as a diagnostic test for HPV-16 infection. However, the assay appears to have adequate specificity and should be useful as an epidemiological marker of HPV-16 infection and sexual behavior.
采用基于人乳头瘤病毒16型(HPV - 16)病毒样颗粒(VLP)的酶联免疫吸附测定(ELISA),检测376名性活跃的大学女性血清中衣壳蛋白抗体。同时,通过聚合酶链反应(PCR)对这些女性进行生殖道HPV检测,并就HPV感染的人口统计学和行为风险因素进行访谈。生殖道存在HPV - 16 DNA的女性血清阳性率为46%。生殖道携带其他HPV类型或未感染HPV的女性相应血清阳性率分别为30%和19%(HPV - 16组与未感染HPV组相比;比值比[OR]为3.7;95%置信区间[CI]为1.5至8.9)。病毒载量高的女性抗体反应显著高于病毒载量低的女性(中位光密度值分别为0.838和0.137,P = 0.009)。在感染与HPV - 16基因远缘或近缘相关HPV类型的女性中,观察到了相当水平的血清反应性。血清反应性与年龄25至30岁(OR为2.3;95% CI为1.2至4.4)、一生中有三个或更多性伴侣(OR为2.9;95% CI为1.1至10)以及有除HPV之外的性传播疾病史(OR为3.1;95% CI为1.5至6.3)显著相关。血清阳性百分比随一生中性伴侣数量呈线性增加,直至有六个以上性伴侣的女性达到35%的平台期(线性趋势χ检验,P < 0.001)。基于HPV - 16 VLP的ELISA敏感性较低,可能限制了该检测作为HPV - 16感染诊断试验的用途。然而,该检测似乎具有足够的特异性,应可作为HPV - 16感染和性行为的流行病学标志物。