HPV Type Distribution in Benign, High-Grade Squamous Intraepithelial Lesions and Squamous Cell Cancers of the Anus by HIV Status

Author:

Chowdhury Sona1,Darragh Teresa2ORCID,Berry-Lawhorn J.3,Isaguliants Maria45ORCID,Vonsky Maxim67ORCID,Hilton Joan8ORCID,Lazar Ann89,Palefsky Joel1

Affiliation:

1. Division of Infectious Diseases, Department of Medicine, University of California, San Francisco, CA 94143, USA

2. Department of Pathology, University of California, San Francisco, CA 94143, USA

3. Department of Medicine, University of California, San Francisco, CA 94143, USA

4. Institute of Microbiology and Virology, Riga Stradins University, LV-1007 Riga, Latvia

5. Department of Microbiology, Tumor and Cell Biology, Karolinska Institutet, SE-171 77 Stockholm, Sweden

6. D.I. Mendeleyev Institute for Metrology, 190005 St. Petersburg, Russia

7. Almazov National Medical Research Center, 197341 St. Petersburg, Russia

8. Department of Epidemiology and Biostatistics, University of California, San Francisco, CA 94143, USA

9. Division of Oral Epidemiology, University of California, San Francisco, CA 94143, USA

Abstract

The incidence of anal cancer is increasing, especially in high-risk groups, such as PLWH. HPV 16, a high-risk (HR) HPV genotype, is the most common genotype in anal high-grade squamous intraepithelial lesions (HSIL) and squamous cell carcinoma (SCC) in the general population. However, few studies have described the distribution of HR HPV genotypes other than HPV 16 in the anus of PLWH. HPV genotyping was performed by DNA amplification followed by dot-blot hybridization to identify the HR and low-risk (LR) genotypes in benign anal lesions (n = 34), HSIL (n = 30), and SCC (n = 51) of PLWH and HIV-negative individuals. HPV 16 was the most prominent HR HPV identified, but it was less common in HSIL and SCC from PLWH compared with HIV-negative individuals, and other non-HPV 16 HR HPV (non-16 HR HPV) types were more prevalent in samples from PLWH. A higher proportion of clinically normal tissues from PLWH were positive for one or more HPV genotypes. Multiple HPV infection was a hallmark feature for all tissues (benign, HSIL, SCC) of PLWH. These results indicate that the development of anal screening approaches based on HPV DNA testing need to include non-16 HR HPVs along with HPV 16, especially for PLWH. Along with anal cytology, these updated screening approaches may help to identify and prevent anal disease progression in PLWH.

Funder

National Institute of Health

National Cancer Institute

Latvian Council of Science

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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