Sasagawa T, Yamazaki H, Dong Y Z, Satake S, Tateno M, Inoue M
Department of Obstetrics and Gynecology, Kanazawa University, School of Medicine, Ishikawa, Japan.
Int J Cancer. 1998 Feb 9;75(4):529-35. doi: 10.1002/(sici)1097-0215(19980209)75:4<529::aid-ijc7>3.0.co;2-v.
Immunoglobulin-A and -G (IgA and IgG) responses against HPV-16-like particles (VLP) were tested by ELISA in 104 women with cervical abnormalities, 26 atypical cells of undetermined significance (ASCUS) and 14 cytologically normal women with HPV DNA. As controls, 130 age-matched cytologically normal women with no HPV DNA were selected from the population in which the cases were generated. The existence of HPV DNA in cervical samples was tested by a PCR-based method. The normal women positive with HPV-16 DNA were followed up at 4- to 7-month intervals for 16 to 24 months. IgA and IgG antibodies against HPV-16 VLP were frequently detected in these women repeatedly positive with HPV-16 DNA, suggesting that persistent HPV infection is crucial for effective antibody responses against the viruses. IgA response appears earlier and persists longer than IgG response. Women with HPV DNA of types 16, 31/33/35, 58 and unknown types showed significantly higher seropositivity for both IgA and IgG antibodies than the controls (p < 0.05 for both). No significant seropositivity for IgA or IgG was detected in the HPV-18/45-DNA-positive group. HPV 31/33/35, 58 appear to be types close to HPV 16, whereas HPV 18/45 appears to be distinct from HPV 16 in antigenicity. IgA and IgG responses against HPV-16 VLP were more frequently observed in women with normal cervices with HPV DNA, ASCUS, HSIL and cervical cancer than in the controls. Strong IgA and IgG responses depended on HPV-16 infection in HSIL and cervical cancer, but there was no correlation between the serological responses and the status of HPV DNA in ASCUS and LSIL. Antibody positivity reflects persistent viral infection that may increase the risk for malignant progression of the cervix. This serological assay using HPV-16 VLP may therefore be useful as a new diagnostic tool supplementing cervical cytological tests.
采用酶联免疫吸附测定(ELISA)法检测了104例宫颈异常女性、26例意义不明确的非典型细胞(ASCUS)女性以及14例HPV DNA检测呈阳性的细胞学正常女性针对人乳头瘤病毒16型样颗粒(VLP)的免疫球蛋白A和G(IgA和IgG)反应。作为对照,从病例来源人群中选取了130例年龄匹配、HPV DNA检测呈阴性的细胞学正常女性。采用基于聚合酶链反应(PCR)的方法检测宫颈样本中HPV DNA的存在情况。对HPV - 16 DNA检测呈阳性的正常女性每隔4至7个月进行随访,为期16至24个月。在这些HPV - 16 DNA检测多次呈阳性的女性中,经常检测到针对HPV - 16 VLP的IgA和IgG抗体,这表明持续的HPV感染对于产生有效的抗病毒抗体反应至关重要。IgA反应比IgG反应出现得更早且持续时间更长。HPV 16型、31/33/35型、58型及类型不明的HPV DNA阳性女性的IgA和IgG抗体血清阳性率均显著高于对照组(两者p均<0.05)。在HPV - 18/45 - DNA阳性组中未检测到显著的IgA或IgG血清阳性。HPV 31/33/35型、58型似乎与HPV 16型相近,而HPV 18/45型在抗原性上似乎与HPV 16型不同。与对照组相比,HPV DNA检测呈阳性的宫颈正常女性、ASCUS女性、高级别鳞状上皮内病变(HSIL)女性及宫颈癌女性中,针对HPV - 16 VLP的IgA和IgG反应更为常见。在HSIL和宫颈癌中,强烈的IgA和IgG反应依赖于HPV - 16感染,但在ASCUS和低级别鳞状上皮内病变(LSIL)中,血清学反应与HPV DNA状态之间无相关性。抗体阳性反映了持续的病毒感染,这可能会增加宫颈恶性进展的风险。因此,这种使用HPV - 16 VLP的血清学检测方法可能作为一种补充宫颈细胞学检查的新型诊断工具。