Comparative testing of HPV L1 protein monoclonal antibody panel for the detection of HPV in cervical exfoliated cells

被引:7
作者
Wang, Le [1 ,2 ,3 ]
Hu, Yu-Chang [1 ]
Xiao, Chang-Yi [1 ,2 ,3 ,4 ]
Wang, Fei [1 ]
Liu, Yu-Fei [1 ]
Tang, Li-Hua [1 ]
Xiao, Rong-Shuang [3 ]
机构
[1] China Three Gorges Univ, Inst Pathol, Yichang 443002, Hubei, Peoples R China
[2] Yichang Cent Peoples Hosp, Cent Lab, Yichang 443003, Hubei, Peoples R China
[3] China Three Gorges Univ, Clin Med Coll 1, Cent Lab, Yichang 443003, Hubei, Peoples R China
[4] China Three Gorges Univ, Med Coll, Yichang 443002, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
Human papillomavirus; Major capsid protein; Monoclonal antibody; Immunological histochemistry; Cervical exfoliated cells; CAPTURE II(R) ASSAYS; HUMAN-PAPILLOMAVIRUS; INTRAEPITHELIAL NEOPLASIA; CANCER PREVENTION; CAPSID PROTEIN; PERFORMANCE; SCREEN;
D O I
10.1016/j.jviromet.2018.03.012
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Aims: To determine the value of a monoclonal antibody panel against a C-terminal conserved sequence poly peptide of human papillomavirus (HPV) L1 (a major capsid protein) for the detection of HPV in cervical exfoliated cells, as well as the potential of this antibody panel to be developed into an assay kit for the clinical screening of cervical cancer. Methods: Cervical exfoliated cells were collected at a gynecology clinic. One part of each sample was sent to the Department of Pathology for HPV genotyping, and the other part was sent to the Department of Pathology for cytologic testing and then to the laboratory for immunological histological chemistry (IHC) assay in which an HPV L1 C-terminal conserved sequence polypeptide-induced mouse monoclonal antibody panel was used to detect HPV L1. Results: Cervical cell samples were collected from 514 patients at the gynecology clinic; of these, 339 samples were sent for HPV genotyping, and 220 were HPV positive (64.90%, 220/339). Moreover, the duplicate samples from these 339 patients were sent for IHC assay, and 229 samples were positive (67.55%, 229/339). The IHC result was concordant with that obtained by HPV genotyping (Kappa = 0.743, p < 0.001). Conclusion: This study showed that use of the HPV L1 C-terminal conserved sequence polypeptide-induced mouse monoclonal antibody panel was of great value for the detection of HPV in cervical cells; the resulting detection rate was comparable to that obtained using the commercial HPV genotyping kit that is currently in use in clinical practice.
引用
收藏
页码:33 / 41
页数:9
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