Mooij Sofie H, Landén Olivia, van der Klis Fiona R M, van der Sande Marianne A B, de Melker Hester E, Xiridou Maria, van Eeden Arne, Heijman Titia, Speksnijder Arjen G C L, Snijders Peter J F, Schim van der Loeff Maarten F
Cluster of Infectious Diseases, Public Health Service of Amsterdam (GGD), Amsterdam, the Netherlands. Center for Infection and Immunity Amsterdam (CINIMA), Department of Internal Medicine, Academic Medical Center, Amsterdam, the Netherlands.
Cluster of Infectious Diseases, Public Health Service of Amsterdam (GGD), Amsterdam, the Netherlands.
Cancer Epidemiol Biomarkers Prev. 2014 Nov;23(11):2455-61. doi: 10.1158/1055-9965.EPI-14-0199. Epub 2014 Aug 28.
We assessed human papillomavirus (HPV) seroconversion following anal and penile HPV infection in HIV-negative and HIV-infected men who have sex with men (MSM).
MSM aged ≥18 years were recruited in Amsterdam, the Netherlands (2010-2011), and followed up semiannually. Antibodies against 7 high-risk HPV types in baseline and 12-month serum samples were tested using a multiplex immunoassay. Baseline, 6-, and 12-month anal and penile samples were tested for HPV DNA using the SPF10-PCR DEIA/LiPA25 system. Statistical analyses were performed using logistic regression with generalized estimating equations.
Of 644 MSM included in the analysis, 245 (38%) were HIV-infected. Median age was 38 years for HIV-negative and 47 years for HIV-infected MSM (P < 0.001). Seroconversion against ≥1 of the 7 HPV types was observed in 74 of 396 (19%) HIV-negative and 52 of 223 (23%) HIV-infected MSM at risk (P = 0.2). Incident [adjusted OR (aOR) 2.0; 95% confidence interval (CI), 1.1-3.4] and persistent (aOR 3.7; 95% CI, 1.5-9.5) anal HPV infections were independently associated with type-specific seroconversion in HIV-negative MSM. In HIV-infected MSM, there was a nonsignificant positive association between penile HPV infection at any time point and seroconversion (aOR 1.7; 95% CI, 0.9-3.2).
Incident or persistent anal HPV infection was an independent determinant of seroconversion in HIV-negative MSM.
Our data support that seroresponse may vary per anatomic site and that persistent HPV infections are more likely to elicit a detectable humoral immune response.
我们评估了在未感染HIV和感染HIV的男男性行为者(MSM)中,肛门和阴茎感染人乳头瘤病毒(HPV)后的血清转化情况。
2010年至2011年在荷兰阿姆斯特丹招募了年龄≥18岁的MSM,并每半年进行一次随访。使用多重免疫测定法检测基线和12个月血清样本中针对7种高危HPV类型的抗体。使用SPF10-PCR DEIA/LiPA25系统检测基线、6个月和12个月时的肛门和阴茎样本中的HPV DNA。使用广义估计方程的逻辑回归进行统计分析。
纳入分析的644名MSM中,245名(38%)感染了HIV。未感染HIV的MSM中位年龄为38岁,感染HIV的MSM中位年龄为47岁(P<0.001)。在有风险的396名未感染HIV的MSM中,74名(19%)出现了针对7种HPV类型中至少1种的血清转化;在223名感染HIV的MSM中,52名(23%)出现了血清转化(P = 0.2)。新发(校正比值比[aOR] 2.0;95%置信区间[CI],1.1 - 3.4)和持续性(aOR 3.7;95% CI,1.5 - 9.5)肛门HPV感染与未感染HIV的MSM中特定类型的血清转化独立相关。在感染HIV的MSM中,任何时间点的阴茎HPV感染与血清转化之间存在无统计学意义的正相关(aOR 1.7;95% CI,0.9 - 3.2)。
新发或持续性肛门HPV感染是未感染HIV的MSM血清转化的独立决定因素。
我们的数据支持血清反应可能因解剖部位而异,并且持续性HPV感染更有可能引发可检测到的体液免疫反应。