The effect of human immunodeficiency virus and human papillomavirus strain diversity on the progression of anal squamous intraepithelial lesions

被引:2
作者
Bushara, Omar [1 ]
Weinberg, Samuel Edward [1 ]
Finkelman, Brian Steven [1 ]
Jiang, Hongmei [2 ]
Krogh, Katrina [1 ]
Sun, Leyu [1 ]
Halverson, Amy L. [3 ]
Jennings, Lawrence J. [1 ]
Liao, Jie [1 ]
Yang, Guang-Yu [1 ,4 ]
机构
[1] Northwestern Univ Feinberg, Sch Med, Dept Pathol, 303 Chicago Ave, Chicago, IL 60611 USA
[2] Northwestern Univ, Dept Stat, 2006 Sheridan Rd, Evanston, IL 60208 USA
[3] Northwestern Univ Feinberg, Sch Med, Dept Surg, 303, Chicago Ave, Chicago, IL 60611 USA
[4] Northwestern Univ Feinberg, Sch Med, Dept Pathol, 303 E Chicago Ave, Ward Bldg 4 115, Chicago, IL 60611 USA
关键词
Anal cancer; Squamous cell carci-noma; Anal dysplasia; HIV; HPV; HIV-1 TAT PROTEIN; TYPE-16; E6; CANCER; EPIDEMIOLOGY; INFECTION; HAART; MEN; SEX;
D O I
10.1016/j.humpath.2022.06.025
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Anal squamous cell carcinoma (SCC) is a human papillomavirus (HPV)-mediated malig-nancy with increasing incidence. Human immunodeficiency virus (HIV) infection is a significant risk factor for anal SCC; however, it is unknown if HIV infection alters anal lesion progression and HPV strain profile. This study aims to determine whether HIV coinfection is associated with progression of HPV-mediated anal lesions and on their HPV strain diversity. This is a retrospective cohort study of adults with anal squamous intraepithelial lesion (SIL) who presented for anorectal sampling between 2010 and 2019. Using the full cohort, we performed clinicopathologic epidemiologic analysis of HIV coinfection on lesion progression. Using a subset of patients, we conducted molecular analysis of HPV strain diversity as related to HIV status and progression. Our cohort included 2203 individuals, of which 940 (43%) were HIV+. HIV+ status was associated with faster progression at all levels of dysplasia. Our molecular cohort included 329 adults, of which 190 (57.8%) were HIV+. HIV+ status was associated with higher HPV strain diversity (median: 7 [5-9] versus median: 4 [4-6], P < .001). Latent class analysis identified specific HPV strain signatures associated with progres-sion. We demonstrate that HIV+ individuals had faster rates of anal SIL progression and that almost all HPV strains were more prevalent in anal samples from HIV+ adults. Our results imply that HIV+
引用
收藏
页码:20 / 30
页数:11
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