van Doornum G, Prins M, Andersson-Ellström A, Dillner J
Division of Public Health and Environment, Municipal Health Service of Amsterdam, Netherlands.
Sex Transm Infect. 1998 Oct;74(5):354-60. doi: 10.1136/sti.74.5.354.
We performed a study to establish the pattern of serological reactivity for immunoglobulins (Ig), to capsids of human papilloma virus (HPV) after new HPV infection in two groups of subjects.
The pattern of serological reactivity after acquisition of infection with HPV was investigated by measuring IgA, IgM, and IgG antibodies to capsids containing L1 and L2 proteins of HPV types 6, 11, 16, 18, and 33 in longitudinal studies of groups with different patterns of sexual activity. Individuals who tested negative for HPV DNA by the polymerase chain reaction at enrolment, but who became HPV DNA positive during follow up, were examined for antibodies to HPV capsids by enzyme linked immunosorbent assay. One group consisted of 15 young girls (with eight controls who remained HPV DNA negative) who were becoming sexually active and the other comprised 12 male (with five controls) and 35 female (with seven controls) heterosexual attenders of a sexually transmitted disease clinic who had had multiple sexual partners.
The sexually inexperienced girls showed IgA and IgG responses, but seldom an IgM response to infection with HPV types 6/11, 16, and 18. No consistent pattern of serological reactivity was apparent for the heterosexuals with multiple partners. The lack of association between current HPV DNA positivity and detectable antibodies in these individuals was possibly related to the duration of infection or to prior exposure to HPV. For the latter group serological reactivity to HPV capsids was significantly greater in women than in men (p = 0.001, p = 0.003, and p = 0.024, for IgG to HPV 6, 11, and 16, respectively).
The sex difference in antibody response detected in previous studies with assays based on peptide antigens was thus corroborated in the present study with capsid based serological assays. This sex difference might reflect a difference in sexual activity and prior exposure to HPV between men and women in this particular group.
我们开展了一项研究,以确定两组受试者新感染人乳头瘤病毒(HPV)后,针对HPV衣壳的免疫球蛋白(Ig)血清学反应模式。
在对具有不同性活动模式的人群进行纵向研究中,通过检测针对包含HPV 6、11、16、18和33型L1和L2蛋白的衣壳的IgA、IgM和IgG抗体,研究感染HPV后血清学反应模式。入组时通过聚合酶链反应检测HPV DNA呈阴性,但在随访期间变为HPV DNA阳性的个体,采用酶联免疫吸附测定法检测其针对HPV衣壳的抗体。一组由15名开始有性活动的年轻女孩(8名对照,HPV DNA保持阴性)组成,另一组由12名男性(5名对照)和35名女性(7名对照)组成,这些异性恋者来自一家性传播疾病诊所,有多个性伴侣。
性经验不足的女孩表现出IgA和IgG反应,但很少对HPV 6/11、16和18型感染产生IgM反应。有多个性伴侣的异性恋者没有明显一致的血清学反应模式。这些个体中当前HPV DNA阳性与可检测抗体之间缺乏关联,可能与感染持续时间或既往HPV暴露有关。对于后一组,女性对HPV衣壳的血清学反应明显强于男性(针对HPV 6、11和16型的IgG,p值分别为0.001、0.003和0.024)。
因此,本研究采用基于衣壳的血清学检测方法,证实了先前基于肽抗原检测的研究中所检测到的抗体反应的性别差异。这种性别差异可能反映了该特定群体中男性和女性在性活动及既往HPV暴露方面的差异。