Guerin-Reverchon I, Chardonnet Y, Viac J, Chouvet B, Chignol M C, Thivolet J
INSERM U209, CNRS UA 601, Clinique Dermatologique, Lyon, France.
J Cancer Res Clin Oncol. 1990;116(3):295-300. doi: 10.1007/BF01612906.
Cutaneous Bowen's disease (BD) and genital bowenoid papulosis (BP) are considered as precancerous or cancerous lesions that are sometimes infected with human papillomavirus (HPV). We studied retrospectively paraffin-embedded sections of 11 samples of cutaneous BD and 6 samples of genital BP from the general population for HPV infection and filaggrin expression. Using in situ hybridization with biotinylated probes of HPV types 1, 2, 5, 6, 11, 16, and 18, under stringent and/or non-stringent conditions and a streptavidin-alkaline-phosphatase complex for hybrid detection, HPV DNA was detected in 6/17 cases (5 BD and 1 BP). Positive nuclei were located in intermediate or upper epithelial cell layers. HPV 16 was found in 2 cases of BD but associated either with HPV 2 or 18. Three additional lesions reacted only under non-stringent conditions; HPV could not be typed with the probes used. The positive case of BP reacted with the four probe types 1, 2, 16, 18 and was negative with HPV 6 or 11. Viral antigen was not detected by indirect immunofluorescence with a rabbit antiserum directed to group-specific viral capsid antigen. Differentiation disorders were observed in the intermediate and upper cell layers of these specimens, as shown by a reduced expression of filaggrin/profilaggrin, a marker of terminal differentiation, in extragenital BD (7/11 cases), and an increased expression in genital BP (4/5 cases) although viral DNA was not always detectable. This study shows that in situ hybridization is a valuable technique for HPV DNA detection and its typing in BD and BP lesions on deparaffinized sections. The positive nuclei were located in the cell layers that exhibited abnormal expression of differentiation. There is no relation between the HPV infecting type and the filaggrin expression.
皮肤鲍温病(BD)和生殖器鲍温样丘疹病(BP)被视为癌前或癌性病变,有时感染人乳头瘤病毒(HPV)。我们回顾性研究了来自普通人群的11例皮肤BD样本和6例生殖器BP样本的石蜡包埋切片,以检测HPV感染和丝聚合蛋白表达。使用生物素化的1、2、5、6、11、16和18型HPV探针在严格和/或非严格条件下进行原位杂交,并使用链霉亲和素 - 碱性磷酸酶复合物进行杂交检测,在17例病例中的6例(5例BD和1例BP)检测到HPV DNA。阳性细胞核位于上皮细胞的中层或上层。在2例BD病例中发现HPV 16,但与HPV 2或18相关。另外3个病变仅在非严格条件下有反应;使用的探针无法对HPV进行分型。BP的阳性病例与1、2、16、18四种探针类型有反应,而对HPV 6或11呈阴性。用针对组特异性病毒衣壳抗原的兔抗血清进行间接免疫荧光未检测到病毒抗原。在这些标本的中层和上层细胞层观察到分化异常,表现为在生殖器外BD(7/11例)中终末分化标志物丝聚合蛋白/前丝聚合蛋白表达降低,而在生殖器BP(4/5例)中表达增加,尽管并非总能检测到病毒DNA。本研究表明,原位杂交是检测石蜡切片上BD和BP病变中HPV DNA及其分型的有价值技术。阳性细胞核位于表现出分化异常表达的细胞层。HPV感染类型与丝聚合蛋白表达之间没有关系。