Title
Author
DOI
Article Type
Special Issue
Volume
Issue
Chlamydia trachomatis and herpes simplex virus 2 infection in vul var intraepithelial neoplasia associated with human papillomavirus
1Clinic of Obstetrics and Gynecology, Poland
2Department l!f Pathomorphology, Poland
3Department of Histology, Skubiszewski University School of Medicine, Poland
4Department of Obstetrics and Gynecology, Collegium Medicum N. Copernicus University of To run, Poland
5Department of Molecular Virology, Adam Mickiewicz University, Poznan, Poland
*Corresponding Author(s): A. Kwasniewska E-mail:
Background: The role of viral and bacterial co-infection is stressed in VIN. A view that VIN is a sexually transmitted disease made the area of research larger and stimulated scientists to seek other sexually transmitted factors, among which Chlamydia trachomatis and Herpes simplex are frequently examined.
Purpose: The aim of the study was to evaluate the frequency of occurrence of HPV DNA and the frequency of co-infection with Herpes virus type 2 and Chlamydia trachomatis in VIN.
Material and methods: We identified archival diagnostic phase tissue specimens from 41 cases of vulvar intraepithelial neoplasia III. From the same paraffin blocks containing material from the margins of surgical sections during vulvectomy, normal epithelial tissue fragments were collected. They constituted the control group. Lesion characteristics were examined in comparison with the presence of HPV DNA, HSV-2 and Chlamydia trachomatsis. Identification was performed using PCR.
Results: In the study group HPV infection was found in 75.6% of cases. In 73% of cases it was HPV 16. In the control group we found HPV 16 DNA in only one case (2.43%). In the HPV positive study group HPV 16 was found in 30 (30/31) cases. In only one case (1/31) it was HPV 18 type. In the study group of 41 cases with VIN, HSV-2 infection was found in six cases (14.63%). In comparison with the control group (9.75%) the difference was not statistically significant. The frequency of occurrence of Chlamydia trachomatis in the analyzed study material was 14.63% (6/41) and in the control group it was 9.75% (4/41). The difference was not statistically significant. Statistical analyses of correlations between the occurrence of DNA HPV and HSV-2 as well as of HPV and Chlamydia trachomatis showed no correlation in either case.
Conclusion: No correlation was found between the frequency of occurrence of HPV and HSV-2 and HPV and Chlamydia trachomatis in either group.
VIN; HPV; HSV-2; Chlam汕a trachomatis; Vulvar intraepithelial neoplasia
A. Kwasniewska,E. Korobowicz,J. Visconti,M. Zdunek,M. Szymariski,A. Goidzicka-J6zefiak. Chlamydia trachomatis and herpes simplex virus 2 infection in vul var intraepithelial neoplasia associated with human papillomavirus. European Journal of Gynaecological Oncology. 2006. 27(4);405-408.
[1] Flowers L.C., Wistuba E.A., Scurry J., Muller C.Y., Ashfaq R., Miller D.S. et al.: "Genetic changes during the multistage pathogenesis of human papillomavirus positive and negative vulvar carcinomas". J. Soc. Gynecol. Invest., 1999, 6, 213.
[2] zur Hausen H.: "Papillomaviruses and cancer: from basic studies to clinical application". Nature Rev., 2002, 2, 342.
[3] Scheffner M., Werness B.A., Huibregtse J.M., Levine A.J., Howley P.M.: "The E6 oncoprotein encoded by human papillomavirus types 16 and 18 promotes the degradation of p53". Cell., 1990, 63, 1129.
[4] Munger K., Basile J.R., Duensing S., Eichten A., Gonzales S.L., Grace M., Zacny V.L.: "Biological activities and molecular targets of the human papillomavirus E7 oncoprotein". Oncogene, 2001, 20, 7888.
[5] Hart W.R.: "Simplex (differentiated) VIN: an underappreciated threat". Contemp. Obstet. Gynaecol., 2003, 48, 59.
[6] Hart W.R.: "Vulvar intraepithelial neoplasia; historical aspects and current status". Int. J. Pathol., 2001, 20, 16.
[7] Hart W.R., Young R.H., Dail D.H.: "Tumors and related lesions of the female genital tract; based on the proceedings of the 56th Annual Anatomic Pathology Slide Seminar of the American Society of Clinical Pathologists". Dallas, ASCP Press, 1991.
[8] Meyers C., Andreansky S.S., Courtney R.J.: "Replication and interaction of herpes simplex virus and human papillomavirus in differencing host epithelial tissue". Virology, 2003, 315, 43.
[9] Tucker R.A., Johnson P.R., Reeves W.: "Using the polymerase chain reaction to genotype human papillomavirus DNAs in samples containing multiple HPVs may produce inaccurate results". J. Viral. Methods, 1993, 43, 321.
[10] IARC. Human Papillomaviruses. IRAC monographs on the evaluation of carcinogenic risks to humans. Vol. 64, Lyon, IARC, 1995.
[11] Bjorge T.B., Dillner J., Anttila T.: "Prospective sero-epidemiological study of role of human papillomavirus in non-cervical anogenital cancer". Br. Med. J., 1997, 315, 646.
[12] Hildesheim A., Han C.-L., Brinton L.: "Human papillomavirus type 16 and risk of pre-invasive and invasive vulvar cancer: results from a seroepidemiological case-control study". Obstet. Gynecol., 1997, 90, 748.
[13] Planner R.S., Hobbs H.B.: "Intraepithelial and invasive neoplasia of the vulva in association with human papillomavirus infection". J. Reprod. Med., 1988, 35, 503.
[14] Hording U., Junge J., Poulsen H., Lundvall F.: "Vulvar Intraepithelial Neoplasia II: a viral disease of undetermined progressive potential". Gynecol. Oneal., 1995, 56, 276.
[15] Adamek K., Szczudrawa A., Basta A., Wsp6listnienie: "VIN i raka inwazyjnego sromu ze sr6dnablokow neoplazja i rakiem inwazyjnym szyjki macicy i lub pochwy, a infekcja HPV w obrebie dolnego odcinka narzu rodnego". Gin. Pol., 2003, 9, 657.
[16] Radolakis A., Di吐omanolis E., Vlachos G., Iconomou Th., Protopappas A., Stefanidis C. et al.: "Vulvar intraepithelial neoplasia (VIN) - diagnostic and therapetic challenges". Eur. J. Gynecol. Oneal., 2003, 24, 317.
[17] van der Avoort J.A., Shirango H., Hoevenaars B. M.,Greffe J.M., de Hullu l.A.,de Wilde P.C. et al.: "Vulvar Squainous cell carcinoma is a multifocale disease following two separate and independent pathways". Int. J. Gynecol. Pathol., 2006, 25, 22.
[18] Hillemanns P., Wang X.: "Integration of HPV-16 and HPV-18 DNA in vulvar intraepitehelial neoplasia". Gynecol. Oneal., 2006, 100, 276.
[19] Lehtinen M., Koskela P., Jellum E., Bloigu A., Antilla T., Hallmans G., Luukkaala T. et al.: "Herpes simplex virus and risk of cervical cancer: a longitudinal, nested case-control study in the nordic countries". Am. J. Epidemiol., 2002, 156, 687.
[20] Tran-Thanh D., Provencher D., Koushik A., Duarte-Franco E., Kessous A., Drouin P. et al.: "Herpes simplex virus type II is not cofactor to human papillomavirus in cancer of the uterine cervix". Am. J. Obstet. Gynecol., 2003, 188, 129.
[21] Smith J.S., Herrero R., Bosetti C., Munoz N., Bosch F.X., ElufNeto J., Castellsouge X. et al.: "Herpes simplex virus-2 as a human papillomavirus cofactor in the etiology of invasive cervical cancer". J. Natl. Cancer Inst., 2002, 94, 1604.
[22] Costa S., Rotola A., Terzano P., Poggi M.G., Di Luca D., Aurelian L. et al.: "Search for herpes simplex virus 2 and human papillomavirus genetic expression in vulvar neoplasia". J. Reprod. Med., 1990, 35, 1108.
[23] K wasniewska A., Semczuk M., Kuzma D., Teresinska D.,Gozdzicka-J6zefiak A.: "Czestosc wystepowania HPV i Chlamydia trachomatis w kom6rkach sromu kobiet asymptomatycznych". Pol. Przeg. Gin. Pol., 2003, 3, 139.
[24] YangY.Y., Koh W., Tsai H., Wong E.F., Lin S.J., Yang C.C.: "Correlation of viral factors with cervical cancer in Taiwan". J. Microbiol. lmmunol. Infect., 2004, 37, 282.
Science Citation Index Expanded (SciSearch) Created as SCI in 1964, Science Citation Index Expanded now indexes over 9,500 of the world’s most impactful journals across 178 scientific disciplines. More than 53 million records and 1.18 billion cited references date back from 1900 to present.
Biological Abstracts Easily discover critical journal coverage of the life sciences with Biological Abstracts, produced by the Web of Science Group, with topics ranging from botany to microbiology to pharmacology. Including BIOSIS indexing and MeSH terms, specialized indexing in Biological Abstracts helps you to discover more accurate, context-sensitive results.
Google Scholar Google Scholar is a freely accessible web search engine that indexes the full text or metadata of scholarly literature across an array of publishing formats and disciplines.
JournalSeek Genamics JournalSeek is the largest completely categorized database of freely available journal information available on the internet. The database presently contains 39226 titles. Journal information includes the description (aims and scope), journal abbreviation, journal homepage link, subject category and ISSN.
Current Contents - Clinical Medicine Current Contents - Clinical Medicine provides easy access to complete tables of contents, abstracts, bibliographic information and all other significant items in recently published issues from over 1,000 leading journals in clinical medicine.
BIOSIS Previews BIOSIS Previews is an English-language, bibliographic database service, with abstracts and citation indexing. It is part of Clarivate Analytics Web of Science suite. BIOSIS Previews indexes data from 1926 to the present.
Journal Citation Reports/Science Edition Journal Citation Reports/Science Edition aims to evaluate a journal’s value from multiple perspectives including the journal impact factor, descriptive data about a journal’s open access content as well as contributing authors, and provide readers a transparent and publisher-neutral data & statistics information about the journal.
Top