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原位杂交与免疫组化技术检测子宫颈病变中人乳头瘤病毒的对比研究

Comparative study of in situ hybridization and immunohistochemical techniques for the detection of human papillomavirus in lesions of the uterine cervix.

作者信息

Alonso M J, Gomez F, Muñoz E, Abad M M, Roldan M, Curiel I, Paz J I, Bullon A, Lopez-Bravo A

机构信息

Department of Pathology, Institute of Health Carlos III, Madrid, Spain.

出版信息

Eur J Histochem. 1992;36(3):271-8.

PMID:1281009
Abstract

Among the techniques currently used for the detection of human papillomavirus (HPV) in genital lesions, only two correlate HPV with the histopathological findings of the lesion: immunohistochemistry and in situ hybridization. Consequently, we were prompted to carry out a comparative study on both techniques to check their utility and efficacy as routine diagnostic methods. 52 biopsy specimens of uterine cervix diagnosed histopathologically as condylomas and cervical intraepithelial neoplasia+koilocytosis were studied by immunohistochemical and in situ hybridization techniques using a polyclonal antibody against the common antigen of the HPV capsid and three biotinylated DNA probes specific to HPV types 6/11, 16/18 and 31/35/51. Immunohistochemistry detected 21 positive cases (40.38%), whereas in situ hybridization detected 40 positive cases (76.92%); of the latter, 30 were positive for HPV types 6/11, 3 for HPV types 16/18 and 11 for HPV types 31/35/51. The results suggest that in situ hybridization is a more sensitive technique than immunohistochemistry. However, we recommend the use of both techniques in the case of potentially malignant lesions since better prognostic information can be obtained from joint analysis of both results.

摘要

在目前用于检测生殖器病变中人类乳头瘤病毒(HPV)的技术中,只有两种技术将HPV与病变的组织病理学结果相关联:免疫组织化学和原位杂交。因此,我们开展了一项针对这两种技术的比较研究,以检验它们作为常规诊断方法的实用性和有效性。我们使用一种针对HPV衣壳共同抗原的多克隆抗体以及三种分别针对HPV 6/11型、16/18型和31/35/51型的生物素化DNA探针,通过免疫组织化学和原位杂交技术对52例经组织病理学诊断为尖锐湿疣和宫颈上皮内瘤变伴挖空细胞的子宫颈活检标本进行了研究。免疫组织化学检测出21例阳性病例(40.38%),而原位杂交检测出40例阳性病例(76.92%);在后者中,30例为HPV 6/11型阳性,3例为HPV 16/18型阳性,11例为HPV 31/35/51型阳性。结果表明,原位杂交是一种比免疫组织化学更敏感的技术。然而,对于潜在恶性病变,我们建议同时使用这两种技术,因为通过联合分析两者结果可以获得更好的预后信息。

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