Ho Gloria Y F, Studentsov Yevgeniy Y, Bierman Robert, Burk Robert D
Department of Epidemiology and Population Health, Albert Einstein College of Medicine, Bronx, New York, USA.
Cancer Epidemiol Biomarkers Prev. 2004 Jan;13(1):110-6. doi: 10.1158/1055-9965.epi-03-0191.
Immunization with a vaccine of human papillomavirus (HPV) type 16 virus-like particles (VLPs) can reduce incidence of HPV-16 infection and its related cervical intraepithelial neoplasia. However, development of detectable antibodies to VLPs does not always occur after natural HPV infection. This study examined prospectively for seroconversion and duration of antibodies to HPV-16 VLPs and their associated host and viral factors. Six-hundred eight subjects were tested for HPV DNA biannually and for IgG and IgA antibodies to HPV-16 VLPs annually for 3 years. Both IgG and IgA antibodies to HPV-16 VLPs were predominantly type specific. Women with cervicovaginal HPV-16 infection were 8-10 times more likely to seroconvert than those with infection of HPV-16-related types. Among subjects who had an incident infection with HPV-16, a maximum of 56.7% became seropositive for IgG within 8.3 months and 37.0% had IgA within 14 months. Detectable seroconversion was a slow process that required sufficient antigenic exposure associated with either a high viral load (relative risk = 5.7 for IgG) or persistent infection of HPV-16 (relative risk = 3.4 for IgA). The median duration for both types of antibodies was approximately 36 months. Antibodies could persist for a long period of time if the initial antibody levels were high or if there was continued antigenic exposure.
用16型人乳头瘤病毒(HPV)病毒样颗粒(VLP)疫苗进行免疫接种可降低HPV - 16感染及其相关宫颈上皮内瘤变的发生率。然而,自然HPV感染后并非总能产生可检测到的针对VLP的抗体。本研究前瞻性地检测了针对HPV - 16 VLP的血清转化情况、抗体持续时间及其相关的宿主和病毒因素。608名受试者每半年检测一次HPV DNA,连续3年每年检测针对HPV - 16 VLP的IgG和IgA抗体。针对HPV - 16 VLP的IgG和IgA抗体主要具有型特异性。宫颈阴道HPV - 16感染的女性血清转化的可能性比感染HPV - 16相关型别的女性高8至10倍。在HPV - 16新发感染的受试者中,最多56.7%在8.3个月内IgG呈血清阳性,37.0%在14个月内IgA呈阳性。可检测到的血清转化是一个缓慢的过程,需要与高病毒载量(IgG的相对风险 = 5.7)或HPV - 16持续感染(IgA的相对风险 = 3.4)相关的足够抗原暴露。两种抗体的中位持续时间约为36个月。如果初始抗体水平高或存在持续抗原暴露,抗体可能会持续很长时间。