Van Doornum G J, Prins M, Pronk L, Coutinho R A, Dillner J
Department of Public Health, Municipal Health Service of Amsterdam, The Netherlands.
Clin Diagn Lab Immunol. 1994 Nov;1(6):633-9. doi: 10.1128/cdli.1.6.633-639.1994.
The aim of this study was to investigate whether antibody responses against synthetic peptides derived from genital human papillomavirus (HPV) proteins are associated with laboratory-proven genital and anorectal HPV infection. In this study, 158 heterosexual patients (110 women and 48 men) were followed prospectively. At each visit we collected serum samples as well as specimens from several sites in the anogenital area for detection of HPV type 6/11 (HPV-6/11), -16, -18, and -33 DNAs by PCR. Immunoglobulin A (IgA) and IgG responses against disrupted bovine papilloma virions and eight different synthetic peptides derived from HPV-6/11, -16, and -18 were determined for serum samples from the first and the last visits. The subjects attended the Municipal Sexually Transmitted Disease Clinic in Amsterdam, The Netherlands, two to seven times (mean, four times) at approximately 4-month intervals. Women were monitored over a period of 155 person-years, and men were monitored over 65 person-years. The magnitudes of the IgA responses against HPV-16 late protein epitopes L1:13, L1:31, and L2:49 were significantly higher in the sera from the last visit among the currently HPV DNA-positive participants than in HPV DNA-negative persons (P = 0.02). When the persons positive for any HPV type at any time during the follow-up period were compared with those who were negative at all times during the follow-up period, we also found a significant elevation of IgA responses against L1:31 and L2:49 (P = 0.04 and 0.01, respectively).(ABSTRACT TRUNCATED AT 250 WORDS)
本研究的目的是调查针对源自生殖器人乳头瘤病毒(HPV)蛋白的合成肽的抗体反应是否与经实验室证实的生殖器和肛门直肠HPV感染相关。在本研究中,对158名异性恋患者(110名女性和48名男性)进行了前瞻性随访。每次就诊时,我们收集血清样本以及来自肛门生殖器区域多个部位的标本,通过聚合酶链反应(PCR)检测HPV 6/11型(HPV-6/11)、-16、-18和-33的DNA。针对第一次和最后一次就诊时的血清样本,测定了针对破碎牛乳头瘤病毒颗粒以及源自HPV-6/11、-16和-18的八种不同合成肽的免疫球蛋白A(IgA)和IgG反应。这些受试者约每4个月到荷兰阿姆斯特丹市性传播疾病诊所就诊两到七次(平均四次)。对女性进行了155人年的监测,对男性进行了65人年的监测。在目前HPV DNA阳性参与者末次就诊的血清中,针对HPV-16晚期蛋白表位L1:13、L1:31和L2:49的IgA反应强度显著高于HPV DNA阴性者(P = 0.02)。当将随访期间任何时候任何HPV型阳性的人与随访期间一直阴性的人进行比较时,我们还发现针对L1:31和L2:49的IgA反应显著升高(分别为P = 0.04和0.01)。(摘要截短于250字)