Law C L, Qassim M, Thompson C H, Rose B R, Grace J, Morris B J, Cossart Y E
STD Centre, Sydney Hospital.
Genitourin Med. 1991 Apr;67(2):92-8. doi: 10.1136/sti.67.2.92.
(I) to determine the relative sensitivities of clinical examination, cytology and HPV DNA hybridisation for the detection of anal human papillomavirus infection; and (ii) to examine various factors which may influence presentation of anal human papillomavirus infection in homosexual men.
112 unselected homosexual men attending a Sydney STD clinic for routine screening underwent a complete anogenital and physical examination, during which blood samples (for haematological, serological and immunological investigations), rectal swabs (for culture of anal pathogens) and anal scrapes of the dentate line (for cytology and HPV DNA hybridisation) were collected. Papanicolaou-stained anal smears were examined for cytological abnormalities, including those indicative of HPV infection or anal intraepithelial neoplasia (AIN). HPV DNA was detected by high stringency dot hybridisations using radiolabelled HPV 6, 11, 16 and 18 DNA probes. Visible anal condylomata, situated either externally or in the anal canal, were present in 26% of these men; 46% had cytological evidence of HPV infection, and 19% of the smears showed evidence of mild to moderate dysplastic changes (AIN I-II). Detectable HPV DNA was present in 40% of the anal scrapes. By combining these results, a total of 73 men (65%) were found to have at least one of the indicators of HPV infection. These data, together with that relating to HIV antibody, immune status and past or present infection with other STDs, was correlated with information obtained from a questionnaire administered to the patients at the time of their clinical examination.
In this study cytology was found to be slightly more sensitive than HPV DNA dot hybridisation for the detection of HPV infection in the anal canal, providing the full range of HPV-associated cytological changes were accepted as a basis for diagnosis. Clinical anal lesions were more likely to be detected in young men, men who had symptomatic HIV infection and those with a history of past anal wart infection. The latter group also had a higher incidence of cytologically apparent HPV infection in their anal smears. There was a significant association between the detection of HPV 16/18 and the presence of anal dysplasia, but there were no significant correlations between HPV infection or anal dysplasia and HIV antibody, immune function status, sexual practices or history of other STDs.
(i)确定临床检查、细胞学检查和人乳头瘤病毒(HPV)DNA杂交检测肛门人乳头瘤病毒感染的相对敏感性;(ii)研究可能影响男同性恋者肛门人乳头瘤病毒感染表现的各种因素。
112名未经过挑选、前往悉尼性传播疾病诊所进行常规筛查的男同性恋者接受了完整的肛门生殖器及体格检查,在此期间采集了血样(用于血液学、血清学和免疫学检查)、直肠拭子(用于培养肛门病原体)以及齿状线处的肛门刮片(用于细胞学检查和HPV DNA杂交)。对巴氏染色的肛门涂片进行细胞学异常检查,包括那些提示HPV感染或肛门上皮内瘤变(AIN)的异常。使用放射性标记的HPV 6、11、16和18 DNA探针通过高严谨度斑点杂交检测HPV DNA。在这些男性中,26%有可见的肛门湿疣,位于肛门外部或肛管内;46%有HPV感染的细胞学证据,19%的涂片显示有轻度至中度发育异常改变(AIN I-II)。40%的肛门刮片中可检测到HPV DNA。综合这些结果,共有73名男性(65%)被发现至少有一项HPV感染指标。这些数据,连同与HIV抗体、免疫状态以及过去或现在其他性传播疾病感染相关的数据,与在临床检查时向患者发放的问卷所获得的信息进行了关联。
在本研究中,发现对于肛管内HPV感染的检测,细胞学检查比HPV DNA斑点杂交略敏感,前提是将所有与HPV相关的细胞学改变都作为诊断依据。临床肛门病变在年轻男性、有症状HIV感染的男性以及有既往肛门疣感染史的男性中更易被检测到。后一组男性的肛门涂片细胞学上明显的HPV感染发生率也更高。HPV 16/18的检测与肛门发育异常的存在之间存在显著关联,但HPV感染或肛门发育异常与HIV抗体、免疫功能状态、性行为或其他性传播疾病史之间无显著相关性。