Departments of Obstetrics and Gynecology, Yongin Severance Hospital, Yonsei University College of Medicine, Yongin, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, Korean Cancer Center Hospital, Korean Institute of Radiological and Medical Sciences, Seoul, and Inha University Hospital, Inha University College of Medicine, Incheon, and the Department of Laboratory Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
Obstet Gynecol. 2013 Feb;121(2 Pt 1):321-329. doi: 10.1097/AOG.0b013e31827c59f7.
To estimate the clinical significance of serum anti-human papillomavirus (HPV) antibodies and high-risk cervical HPV DNA in cervical neoplasia.
The study population comprised patients who were histopathologically diagnosed with cervical intraepithelial neoplasia (CIN) 1 (n=64), CIN 2 and 3 (n=241), cervical cancer (n=170), and normal control participants (n=975). Cervical HPV DNA tests were performed through nucleic acid hybridization assay tests, and serum anti-HPV 16 and 18 antibodies were measured by competitive immunoassay. The associations of HPV DNA and anti-HPV antibodies were evaluated with demographic characteristics and compared according to the levels of disease severity. Anti-HPV antibodies were also investigated with clinicopathologic parameters, including survival data.
Among various demographic characteristics, factors involving sexual behavior had a higher tendency of HPV DNA positivity and HPV seropositivity. Human papillomavirus DNA mean titer and positivity were both increased in patients with cervical neoplasia compared with those with normal control participants, but there was no statistical difference among types of cervical neoplasia. Serum anti-HPV 16 antibodies were also able to differentiate cervical neoplasia from a normal control participant and furthermore distinguished CIN 1 from CIN 2 and 3 (odd ratio 2.87 [1.43-5.78], P=.002). In cervical cancer, HPV 16 seropositivity was associated with prolonged disease-free survival according to the univariable analysis (hazard ratio=0.12 [0.01-0.94], P=.044).
Serum anti-HPV 16 antibodies can distinguish cervical neoplasia from a normal control and has the advantage of identifying high-grade CIN. Moreover, in cervical cancer, HPV 16 seropositivity may be associated with a more favorable prognosis.
II.
评估血清抗人乳头瘤病毒(HPV)抗体和高危型宫颈 HPV DNA 在宫颈癌前病变中的临床意义。
研究人群包括经组织病理学诊断为宫颈上皮内瘤变(CIN)1 级(n=64)、CIN 2 和 3 级(n=241)、宫颈癌(n=170)和正常对照参与者(n=975)的患者。通过核酸杂交试验进行宫颈 HPV DNA 检测,采用竞争免疫法检测血清抗 HPV 16 和 18 抗体。根据疾病严重程度比较 HPV DNA 和抗 HPV 抗体与人口统计学特征的相关性。还对与临床病理参数相关的 HPV 抗体进行了研究,包括生存数据。
在各种人口统计学特征中,涉及性行为的因素 HPV DNA 阳性和 HPV 血清阳性的倾向更高。与正常对照组相比,宫颈癌患者的 HPV DNA 平均滴度和阳性率均升高,但不同类型的宫颈癌之间无统计学差异。血清抗 HPV 16 抗体也能够将宫颈癌前病变与正常对照组区分开来,并且能够将 CIN 1 与 CIN 2 和 3 区分开来(比值比 2.87[1.43-5.78],P=.002)。在宫颈癌中,根据单变量分析,HPV 16 血清阳性与无病生存时间延长相关(危险比=0.12[0.01-0.94],P=.044)。
血清抗 HPV 16 抗体可将宫颈癌前病变与正常对照组区分开来,并且具有识别高级别 CIN 的优势。此外,在宫颈癌中,HPV 16 血清阳性可能与更好的预后相关。
II。