High-risk human papillomavirus infection involving multiple anatomic sites of the female Lower genital tract: a multiplex real-time polymerase chain reaction-based study

被引:6
作者
Hui, Yiang [1 ,2 ]
Manna, Pradip [3 ]
Ou, Joyce J. [1 ,2 ]
Kerley, Spencer [3 ]
Zhang, Cunxian [4 ]
Sung, C. James [1 ,2 ]
Lawrence, W. Dwayne [1 ,2 ]
Quddus, M. Ruhul [1 ,2 ]
机构
[1] Brown Univ, Alpert Med Sch, Dept Pathol & Lab Med, Providence, RI 02905 USA
[2] Brown Univ, Women & Infants Hosp, Providence, RI 02905 USA
[3] Phys Reference Lab, Overland Pk, KS 66210 USA
[4] Kent Hosp, Warwick, RI 02886 USA
关键词
hrHPV; Multifocal infection; Multisubtype infection; CIN; YIN; VAIN; CERVICAL INTRAEPITHELIAL NEOPLASIA; HPV TYPES; CROSS-PROTECTION; GENOTYPES; WOMEN; PREVALENCE; TYPE-16; LESIONS; CANCER; LOAD;
D O I
10.1016/j.humpath.2015.05.022
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
High-risk human papillomavirus infection usually is seen at one anatomic site in an individual. Rarely, infection at multiple anatomic sites of the female lower genital tract in the same individual is encountered either simultaneously and/or at a later date. The current study identifies the various subtypes of high-risk human papillomavirus infection in these scenarios and analyzes the potential significance of these fmdings. High-risk human papillomavirus infection involving 22 anatomic sites from 7 individuals was identified after institutional review board approval. Residual paraffin-embedded tissue samples were retrieved, and all 15 high-risk human papillomavirus were identified and viral load quantified using multiplex real-time polymerase chain reaction based method. Multiple high-risk human papillomavirus subtypes were identified in 32% of the samples and as many as 5 different subtypes of high-risk human papillomavirus infection in a single anatomic site. In general, each anatomic site has unique combination of viral subtypes, although one individual showed overlapping subtypes in the vagina, cervix, and vulvar samples. Higher viral load and rare subtypes are more frequent in younger patients and in dysplasia compared with carcinoma. Follow-up ranging from 3 to 84 months revealed persistent high-risk human papillomavirus infection in 60% of cases. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:1376 / 1381
页数:6
相关论文
共 34 条
[1]   Are 20 human papillomavirus types causing cervical cancer? [J].
Arbyn, Marc ;
Tommasino, Massimo ;
Depuydt, Christophe ;
Dillner, Joakim .
JOURNAL OF PATHOLOGY, 2014, 234 (04) :431-435
[2]   Genotypes and Prevalence of HPV Single and Multiple Concurrent Infections in Women with HSIL [J].
Beca, Francisco ;
Pinheiro, Jorge ;
Rios, Elisabete ;
Pontes, Patricia ;
Amendoeira, Isabel .
DIAGNOSTIC CYTOPATHOLOGY, 2014, 42 (11) :919-923
[3]   HUMAN PAPILLOMAVIRUS TYPE-16 IN MULTIFOCAL NEOPLASIA OF THE FEMALE GENITAL-TRACT [J].
BECKMANN, AM ;
KIVIAT, NB ;
DALING, JR ;
SHERMAN, KJ ;
MCDOUGALL, JK .
INTERNATIONAL JOURNAL OF GYNECOLOGICAL PATHOLOGY, 1988, 7 (01) :39-47
[4]  
Broccolo F, 2014, METHODS MOL BIOL, V1160, P87, DOI 10.1007/978-1-4939-0733-5_8
[5]   A systematic review of the prevalence of mucosal and cutaneous human papillomavirus types [J].
Bzhalava, Davit ;
Guan, Peng ;
Franceschi, Silvia ;
Dillner, Joakim ;
Clifford, Gary .
VIROLOGY, 2013, 445 (1-2) :224-231
[6]  
Ciotti M, 2006, ONCOL REP, V15, P143
[7]   Influence of HPV type on prognosis in patients diagnosed with invasive cervical cancer [J].
Cuschieri, K. ;
Brewster, D. H. ;
Graham, C. ;
Nicoll, S. ;
Williams, A. R. W. ;
Murray, G. I. ;
Millan, D. ;
Johannessen, I. ;
Hardie, A. ;
Cubie, H. A. .
INTERNATIONAL JOURNAL OF CANCER, 2014, 135 (11) :2721-2726
[8]   HPV vaccine cross-protection: Highlights on additional clinical benefit [J].
De Vincenzo, Rosa ;
Ricci, Caterina ;
Conte, Carmine ;
Scambia, Giovanni .
GYNECOLOGIC ONCOLOGY, 2013, 130 (03) :642-651
[9]   Detection of multiple human papillomavirus types in the lower genital tract correlates with cervical dysplasia [J].
Fife, KH ;
Cramer, HM ;
Schroeder, JM ;
Brown, DR .
JOURNAL OF MEDICAL VIROLOGY, 2001, 64 (04) :550-559
[10]   Reassurance Against Future Risk of Precancer and Cancer Conferred by a Negative Human Papillomavirus Test [J].
Gage, Julia C. ;
Schiffman, Mark ;
Katki, Hormuzd A. ;
Castle, Philip E. ;
Fetterman, Barbara ;
Wentzensen, Nicolas ;
Poitras, Nancy E. ;
Lorey, Thomas ;
Cheung, Li C. ;
Kinney, Walter K. .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2014, 106 (08)