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Head-to-head comparison of genotyping of human papillomavirus by real-time multiplex PCR assay using type-specific primers and SPF10-PCR-based line probe assay
被引:1
|作者:
Yin, Jian
[1
,2
]
Peng, Siying
[2
,3
]
Zhang, Changning
[2
,4
]
Li, Xinyue
[2
]
Hu, Fangfang
[2
,3
]
Chen, Wen
[2
,5
]
Qiao, Youlin
[1
,6
]
机构:
[1] Chinese Acad Med Sci & Peking Union Med Coll, Sch Populat Med & Publ Hlth, Beijing, Peoples R China
[2] Chinese Acad Med Sci & Peking Union Med Coll, Canc Hosp, Natl Clin Res Ctr Canc, Natl Canc Ctr,Dept Canc Epidemiol, Beijing, Peoples R China
[3] Xiamen Univ, Natl Inst Diagnost & Vaccine Dev Infect Dis, Collaborat Innovat Ctr Biol Prod, Sch Publ Hlth,State Key Lab Mol Vaccinol & Mol Dia, Xiamen, Fujian, Peoples R China
[4] Hebei Univ, Coll Life Sci, Baoding, Peoples R China
[5] Chinese Acad Med Sci & Peking Union Med Coll, Canc Hosp, Natl Clin Res Ctr Canc, Natl Canc Ctr,Dept Canc Epidemiol, Beijing 100021, Peoples R China
[6] Chinese Acad Med Sci & Peking Union Med Coll, Sch Populat Med & Publ Hlth, Beijing 100730, Peoples R China
关键词:
cervical cancer;
human papillomavirus;
PCR;
vaccine;
HPV-16/18 AS04-ADJUVANTED VACCINE;
CERVICAL INTRAEPITHELIAL NEOPLASIA;
OF-STUDY ANALYSIS;
HPV TYPES;
EFFICACY;
CANCER;
WOMEN;
TECHNOLOGIES;
ALGORITHM;
INFECTION;
D O I:
10.1002/jmv.28579
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
The SPF10-polymerase chain reaction (PCR)-based line probe assay (LiPA-25) with high analytical sensitivity and specificity for human papillomavirus (HPV) genotyping in clinical samples has been widely used in vaccine and epidemiologic studies. A real-time multiplex PCR assay using type-specific primers (Hybribio-23) with low workload and cost has been developed recently. The study aimed to compare the performance of LiPA-25 and Hybribio-23 in selected 1731 cervical swab and 117 tissue samples, with a focus on 20 common HPV types (14 high-risk: 16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66, and 68/73; 6 low-risk: 6, 11, 42, 43, 44, and 53). The level of agreement of two assays was determined using Cohen's Kappa (& kappa;) statistics. A total of 1296 (74.9%) swab samples were identified as HPV-positive by Hybribio-23 or LiPA-25, of which 814 (62.8%) samples exhibited concordant, 358 (27.6%) showed additional or fewer types (compatible), and 124 (9.6%) were discordant. In addition, the two assays showed a perfect agreement for 20 HPV-combined detection (& kappa; = 0.838) and 17 individual HPV types (all & kappa; > 0.800), a good agreement for HPV31 (& kappa; = 0.792) and 43 (& kappa; = 0.696), and a moderate agreement for HPV42 (& kappa; = 0.504). Hybribio-23 was significantly more sensitive for HPV58, 59, 68/73, 42, 43, and 44, and less sensitive for HPV35 and 66 than LiPA-25 (McNemar's test: all p < 0.05). For 117 HPV-positive tissue specimens, the identification of genotypes was 85.2% identical, 12.2% compatible, and only 2.6% discordant. The agreement for HPV31 (& kappa; = 0.786), 68/73 (& kappa; = 0.742), and HPV53 (& kappa; = 0.742) was good, while for other types (all & kappa; > 0.853) and 20 HPV-combined detection (& kappa; = 0.936) was perfect (all p > 0.05). In conclusion, Hybribio-23 and LiPA-25 are comparable. Hybribio-23 could be used for the detection and genotyping of HPV in cervical samples for epidemiological and vaccine studies worldwide.
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