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宫颈癌患者血清中针对人乳头瘤病毒16型(HPV-16)E6和E7癌蛋白线性及构象表位的抗体

Antibodies against linear and conformational epitopes of the human papillomavirus (HPV) type 16 E6 and E7 oncoproteins in sera of cervical cancer patients.

作者信息

Nindl I, Benitez-Bribiesca L, Berumen J, Farmanara N, Fisher S, Gross G, Lopez-Carillo L, Müller M, Tommasino M, Vazquez-Curiel A

机构信息

Deutsches Krebsforschungszentrum, Forschungsschwerpunkt Angewandte Tumorvirologie, Heidelberg, Federal Republic of Germany.

出版信息

Arch Virol. 1994;137(3-4):341-53. doi: 10.1007/BF01309480.

Abstract

Sera obtained from 137 cervical cancer patients were analysed for the presence of antibodies to the human papillomavirus (HPV) type 16 proteins E6 and E7 by the aid of different assays, i.e. ELISA using as antigen either synthetic peptides or the complete E7 protein and radio-immunoprecipitation (RIPA) which uses the viral protein made by in vitro transcription/translation. In agreement with previous reports, reactivity to the E7 protein was found more frequently than to the E6 protein (31.4% vs. 16.8%) when the sera were assayed by peptide-based ELISA. In contrast, when RIPA was employed, reactivity to either protein was obtained at similar frequency (38.7% vs 46.7%). When the protein was denatured prior to immuno-precipitation the reactivity was lost in all sera tested for E6-specific antibodies but only in a few samples in the E7-RIPA. Therefore it was concluded that the increased sensitivity of the E6-RIPA as compared to the E6 peptide-ELISA is due to the detection of antibodies to conformational epitopes which are presented by the in vitro product but not by the synthetic peptides. Eighty-two sera from healthy donors were tested by HPV 16E6- and E7-RIPA and also by ELISA using the HPV 16E7 protein which was produced in the fission yeast Schizosaccharomyces pombe. One sample reacted each in the E6- and E7-RIPA indicating a high specificity of these assays. The E7 protein-ELISA proved to be less sensitive for the detection of antibodies in cervical cancer patients' sera (22.6% positive) as compared to peptide-based ELISA or RIPA.

摘要

借助不同检测方法,即使用合成肽或完整E7蛋白作为抗原的酶联免疫吸附测定(ELISA)以及使用体外转录/翻译产生的病毒蛋白的放射免疫沉淀法(RIPA),对137例宫颈癌患者的血清进行分析,以检测其针对人乳头瘤病毒(HPV)16型蛋白E6和E7的抗体。与之前的报道一致,当通过基于肽的ELISA检测血清时,发现对E7蛋白的反应性比E6蛋白更常见(31.4%对16.8%)。相比之下,当采用RIPA时,对这两种蛋白的反应性出现频率相似(38.7%对46.7%)。当在免疫沉淀前使蛋白变性时,所有检测E6特异性抗体的血清中反应性均丧失,但在E7-RIPA中仅在少数样本中出现这种情况。因此得出结论,与E6肽-ELISA相比,E6-RIPA灵敏度的提高是由于检测到了针对构象表位的抗体,这些表位由体外产物呈现而非合成肽呈现。通过HPV 16 E6-和E7-RIPA以及使用在裂殖酵母粟酒裂殖酵母中产生的HPV 16 E7蛋白的ELISA对82例健康供体的血清进行检测。在E6-和E7-RIPA中各有一个样本出现反应,表明这些检测方法具有高特异性。与基于肽的ELISA或RIPA相比,E7蛋白-ELISA在检测宫颈癌患者血清中的抗体时灵敏度较低(阳性率为22.6%)。

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