Shah K V, Viscidi R P, Alberg A J, Helzlsouer K J, Comstock G W
Department of Molecular Microbiology, Johns Hopkins School of Public Health, Baltimore, Maryland 21205, USA.
Cancer Epidemiol Biomarkers Prev. 1997 Apr;6(4):233-7.
Our objective was to examine whether past infection with human papillomavirus (HPV)-16, as determined by an antibody assay, is a risk factor for subsequent cervical cancer. Incident cases of in situ or invasive cervical cancer occurring between 1975 and 1990 in a cohort of over 11,000 healthy women in Washington County, MD, were identified. The baseline sera of cases and of matched controls, collected in 1974, were examined for IgG antibodies reactive with virus-like particles of HPV-16, a cancer-associated HPV, and HPV-6, a low-risk HPV. Postdiagnosis sera of 11 cases were also assessed similarly. Fourteen cases of invasive and 28 cases of in situ cervical cancer and 83 matched controls were evaluated. The main outcome measure was the risk of cervical cancer in women who had HPV-16 or HPV-6 antibodies in prediagnostic sera. Antibodies to HPV-16 but not to HPV-6 were a marker for subsequent occurrence of cervical cancer. Case sera were reactive more often and more strongly with HPV-16 virus-like particles than were sera of matched controls. The presence of antibodies to HPV-16 was significantly associated with an increased risk of cervical cancer (odds ratio, 3.9; 95% confidence limits, 1.4, 10.7); high antibody levels to HPV-16 were associated with an even greater risk of cervical cancer (odds ratio = 7.5, 95% confidence limits 1.5, 36.3). The association with cervical cancer was strengthened after adjustment for smoking and years of education. In tests of 11 pairs of pre- and postdiagnostic sera, HPV-16 antibodies did not decline markedly over a 7-13-year time period, and seroconversion to HPV-16 appeared to have occurred in 2 cases. The serological data indicate that HPV-16 infection is associated with future risk of cervical cancer and strengthen the evidence for the etiological role of HPVs in cervical cancer.
我们的目的是通过抗体检测来研究既往感染人乳头瘤病毒16型(HPV-16)是否为后续宫颈癌的一个危险因素。在马里兰州华盛顿县的一个超过11,000名健康女性的队列中,确定了1975年至1990年间发生的原位或浸润性宫颈癌的发病病例。检测了1974年收集的病例组和匹配对照组的基线血清,以检测与癌症相关的HPV-16以及低风险HPV-6的病毒样颗粒发生反应的IgG抗体。还对11例病例的诊断后血清进行了类似评估。评估了14例浸润性宫颈癌、28例原位宫颈癌病例以及83名匹配对照。主要结局指标是诊断前血清中存在HPV-16或HPV-6抗体的女性患宫颈癌的风险。HPV-16抗体而非HPV-6抗体是后续发生宫颈癌的一个标志物。与匹配对照组的血清相比,病例组血清与HPV-16病毒样颗粒发生反应的频率更高、强度更大。HPV-16抗体的存在与宫颈癌风险增加显著相关(比值比为3.9;95%置信区间为1.4至10.7);HPV-16高抗体水平与更高的宫颈癌风险相关(比值比 = 7.5,95%置信区间为1.5至36.3)。在对吸烟和受教育年限进行校正后,与宫颈癌的关联得到加强。在对11对诊断前和诊断后血清的检测中,HPV-16抗体在7至13年的时间段内未显著下降,且有2例出现了HPV-16血清转化。血清学数据表明HPV-16感染与未来宫颈癌风险相关,并强化了HPV在宫颈癌病因学中作用的证据。