Bonnez W, Da Rin C, Rose R C, Tyring S K, Reichman R C
Department of Medicine, University of Rochester School of Medicine and Dentistry, New York 14642.
J Med Virol. 1993 Apr;39(4):340-4. doi: 10.1002/jmv.1890390414.
To evaluate the variation over time of seroreactivity to human papillomavirus type 11 (HPV-11) according to disease outcome, we selected a sample of 42 condyloma acuminatum patients from a group of subjects enrolled in a placebo-controlled trial of three alpha-interferon preparations administered parenterally for the treatment of condyloma acuminatum. This sample included 14 subjects who were cured by the end of follow-up (cured group) and 28 subjects who were not (failed group). For each individual, the first and last sera collected in the study were tested with an intact HPV-11 virion-based enzyme linked immunosorbent assay (ELISA). The sera of 20 nuns with no lifetime sexual exposure served as controls. The median optical density (OD) value of the first serum samples (as well as that of the last samples) from the patients, 0.155, was higher than that of the control sera, 0.073 (P = 2 x 10(-4)). Sensitivity of the assay was 50%. To test if evolution of seroreactivity in the seropositive patients was related to disease outcome after treatment, we examined the average percentage of daily change in OD between the two serum collections. The median OD in the cured group (n = 7) dropped by 0.05% a day whereas in the failed group (n = 11) it increased by 0.07% a day, a highly statistically significant difference (P = 0.006). It is concluded that changes in the seroreactivity to HPV-11 virions are related to outcome of condyloma acumination after treatment. Therefore, improved serological assays may eventually contribute to the monitoring of HPV disease activity.
为了根据疾病转归评估11型人乳头瘤病毒(HPV-11)血清反应性随时间的变化,我们从一组参与三种α干扰素制剂肌肉注射治疗尖锐湿疣的安慰剂对照试验的受试者中选取了42例尖锐湿疣患者作为样本。该样本包括14例在随访结束时治愈的受试者(治愈组)和28例未治愈的受试者(未治愈组)。对每个个体,在研究中收集的首份和末份血清用基于完整HPV-11病毒粒子的酶联免疫吸附测定(ELISA)进行检测。选取20例无终身性接触史的修女血清作为对照。患者首份血清样本(以及末份样本)的中位光密度(OD)值为0.155,高于对照血清的0.073(P = 2×10⁻⁴)。该检测的灵敏度为50%。为了检验血清反应阳性患者血清反应性的变化是否与治疗后的疾病转归相关,我们检测了两次血清采集之间OD每日变化的平均百分比。治愈组(n = 7)的中位OD每天下降0.05%,而未治愈组(n = 11)则每天增加0.07%,差异具有高度统计学意义(P = 0.006)。结论是,对HPV-11病毒粒子血清反应性的变化与尖锐湿疣治疗后的转归相关。因此,改进的血清学检测最终可能有助于监测HPV疾病活动。