Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
Int J Cancer. 2013 Nov;133(9):2172-81. doi: 10.1002/ijc.28215. Epub 2013 May 29.
Only a subset of women with human papillomavirus (HPV) infections will become seropositive, and the factors influencing seroconversion are not well understood. We used a multiplex serology assay in women with mildly abnormal cytology results to examine seroreactivity to oncogenic HPV genotypes. An unbiased subset of women in the atypical squamous cell of undetermined significance /low-grade squamous intraepithelial lesion Triage Study provided blood samples at trial enrollment for serological testing. A Luminex assay based on glutathione s-transferase-L1 fusion proteins as antigens was used to test seroreactivity against eight carcinogenic HPV genotypes (16, 18, 31, 33, 35, 45, 52 and 58). We analyzed the relationship between seroprevalence in women free of precancer (N = 2,464) and HPV DNA status, age, sexual behavior and other HPV-related risk factors. The overall seroprevalence was 24.5% for HPV16 L1 and ∼20% for 18L1 and 31L1. Among women free of precancer, seroprevalence peaked in women less than 29 years and decreased with age. Type-specific seroprevalence was associated with baseline DNA detection for HPV16 (OR = 1.36, 95%CI: 1.04-1.79) and HPV18 (OR = 2.31, 95%CI: 1.61-3.32), as well as for HPV52 and HPV58. Correlates of sexual exposure were associated with increased seroprevalence across most genotypes. Women who were current or former smokers were less likely to be seropositive for all eight of the tested oncogenic genotypes. The multiplex assay showed associations between seroprevalence and known risk factors for HPV infection across nearly all tested HPV genotypes but associations between DNA- and serostatus were weak, suggesting possible misclassification of the participants' HPV serostatus.
只有一部分感染人乳头瘤病毒(HPV)的女性会呈血清阳性,而影响血清转化的因素尚不清楚。我们使用一种多重血清学检测方法,对细胞学结果轻度异常的女性进行检测,以检查对致癌 HPV 基因型的血清反应性。在不典型鳞状细胞意义不明/低级别鳞状上皮内病变分流研究中,一组无偏见的女性在试验入组时提供了血液样本进行血清学检测。一种基于谷胱甘肽 S-转移酶-L1 融合蛋白作为抗原的 Luminex 检测方法用于检测针对八种致癌 HPV 基因型(16、18、31、33、35、45、52 和 58)的血清反应性。我们分析了无癌前病变(N=2464)女性血清阳性率与 HPV DNA 状态、年龄、性行为和其他 HPV 相关危险因素之间的关系。HPV16 L1 的总血清阳性率为 24.5%,18L1 和 31L1 约为 20%。在无癌前病变的女性中,血清阳性率在 29 岁以下的女性中最高,并随年龄增长而下降。特定类型的血清阳性率与 HPV16 的基线 DNA 检测(OR=1.36,95%CI:1.04-1.79)和 HPV18(OR=2.31,95%CI:1.61-3.32)以及 HPV52 和 HPV58 相关。性接触相关因素与大多数基因型的血清阳性率增加有关。当前或曾经吸烟的女性对所有 8 种测试的致癌基因型呈血清阴性的可能性较小。多重检测方法显示,在几乎所有测试的 HPV 基因型中,血清阳性率与 HPV 感染的已知危险因素之间存在关联,但 DNA 状态和血清状态之间的关联较弱,这表明参与者的 HPV 血清状态可能存在错误分类。