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Condomless Receptive Anal Intercourse is Associated with Markers of Mucosal Injury in a Cohort of Men Who Have Sex with Men

23 Pages Posted: 19 Oct 2020

See all articles by Colleen F. Kelley

Colleen F. Kelley

Emory University - Division of Infectious Diseases

Ilana Pollack

Emory University - Division of Infectious Diseases

Rami Yacoub

Emory University - Department of Epidemiology

Zhengyi Zhu

Emory University - Department of Biostatistics & Bioinformatics (BIOS)

Sanjeev Gumber

Emory University - Department of Pathology and Laboratory Medicine

Rama Amara

Emory University - Yerkes National Primate Research Center, Division of Microbiology and Immunology

Veronika Fedirko

Emory University - Department of Epidemiology

Colleen Kraft

Emory University - Department of Pathology and Laboratory Medicine

Tom de Man

MilliporeSigma

Yi-Juan Hu

Emory University - Department of Biostatistics & Bioinformatics (BIOS)

Cassie Grimsley Ackerley

Emory University - Division of Infectious Diseases

Patrick Sullivan

Emory University - Department of Epidemiology

Roberd Bostick

Emory University - Department of Epidemiology

More...

Abstract

Background: The rectal mucosal immune environment among men who have sex with men (MSM) engaging in condomless receptive anal intercourse (CRAI) is immunologically distinct from that of men who do not engage in anal intercourse (AI).

Methods: We enrolled a cohort of MSM engaging in CRAI (n=41) and men who do not engage in AI (controls; n=21) and used standardized, automated immunohistochemistry and quantitative image analysis to investigate the rectal mucosal distribution of neutrophils (MPO), IL-17-producing cells (IL-17), and Tregs (FOXP3) in the lamina propria, and cellullar proliferation (Ki67) and adherens junctions (E-cadherin) in the epithelium. We also examined associations between biomarker expression and the composition of the rectal mucosal microbiota.

Findings: MSM engaging in CRAI had higher mean expression of MPO in the lamina propria (p=0.04) and Ki67 (p=0.04) in the epithelium relative to controls. There were no differences in IL-17, FOXP3, or E-cadherein expression. We found no statistically significant associations of the five biomarkers with the global rectal microbiota composition or with the individual taxa examined.

Interpretation: Increased infiltration of neutrophils and proliferation of crypt epithelial cells may represent an injury response to frequent CRAI in the rectal mucosa of MSM; however, a contributory role of the microbiota to mucosal inflammation among MSM remains unclear. Prevention may be enhanced by interventions that reduce rectal mucosal inflammation or capitalize on the presence of a specific inflammatory mechanism at the time of HIV exposure.

Funding Statement: This study was funded by the National Institutes of Health (K23 AI108335).

Declaration of Interests: All authors declare no conflict of interest.

Ethics Approval Statement: The Institutional Review Board (IRB) at Emory University approved this study.

Keywords: Receptive anal intercourse, mucosal injury, men who have sex with men, immunohistochemistry

Suggested Citation

Kelley, Colleen F. and Pollack, Ilana and Yacoub, Rami and Zhu, Zhengyi and Gumber, Sanjeev and Amara, Rama and Fedirko, Veronika and Kraft, Colleen and de Man, Tom and Hu, Yi-Juan and Grimsley Ackerley, Cassie and Sullivan, Patrick and Bostick, Roberd, Condomless Receptive Anal Intercourse is Associated with Markers of Mucosal Injury in a Cohort of Men Who Have Sex with Men. Available at SSRN: https://ssrn.com/abstract=3710617 or http://dx.doi.org/10.2139/ssrn.3710617

Colleen F. Kelley (Contact Author)

Emory University - Division of Infectious Diseases ( email )

United States

Ilana Pollack

Emory University - Division of Infectious Diseases ( email )

United States

Rami Yacoub

Emory University - Department of Epidemiology ( email )

201 Dowman Drive
Atlanta, GA
United States

Zhengyi Zhu

Emory University - Department of Biostatistics & Bioinformatics (BIOS) ( email )

1518 Clifton Road.
Atlanta, GA 30322
United States

Sanjeev Gumber

Emory University - Department of Pathology and Laboratory Medicine ( email )

Atlanta, GA 30322
United States

Rama Amara

Emory University - Yerkes National Primate Research Center, Division of Microbiology and Immunology ( email )

United States

Veronika Fedirko

Emory University - Department of Epidemiology ( email )

201 Dowman Drive
Atlanta, GA
United States

Colleen Kraft

Emory University - Department of Pathology and Laboratory Medicine ( email )

Atlanta, GA 30322
United States

Tom De Man

MilliporeSigma ( email )

Yi-Juan Hu

Emory University - Department of Biostatistics & Bioinformatics (BIOS) ( email )

1518 Clifton Road.
Atlanta, GA 30322
United States

Cassie Grimsley Ackerley

Emory University - Division of Infectious Diseases ( email )

United States

Patrick Sullivan

Emory University - Department of Epidemiology ( email )

201 Dowman Drive
Atlanta, GA
United States

Roberd Bostick

Emory University - Department of Epidemiology ( email )

201 Dowman Drive
Atlanta, GA
United States