Sex Differences in CMV Replication and HIV Persistence During Suppressive ART

Author:

Gianella Sara1,Tran Sarah McDonald1,Morris Sheldon1,Vargas Millie1,Porrachia Magali1,Oliveira Michelli F1,Lada Steve1,Zhao Mitchell1,Ellsworth Grant B2,Mathad Jyoti S2,Wilkin Timothy2

Affiliation:

1. University of California, San Diego, La Jolla, California, USA

2. Weill Cornell Medicine, New York, USA

Abstract

Abstract Background The association between subclinical cytomegalovirus (CMV) replication and HIV persistence has not been investigated in cis-gender women with HIV. Methods Fifty virologically suppressed female participants with HIV were prospectively enrolled and provided oral, vaginal, and urine samples and peripheral blood mononuclear cells at 1 cross-sectional time point. CMV DNA was quantified in each specimen by real-time polymerase chain reaction (PCR). Cellular HIV DNA and HIV RNA transcripts (unspliced and multiply spliced [ms] encoding tat-rev) were quantified by droplet digital (dd) PCR in peripheral blood cells. Forty-nine male individuals with HIV and CMV (historical data) were used as controls. Results Levels of cellular HIV DNA and unspliced HIV RNA were not different between sexes, but female participants had less detectable msHIV RNA and CMV DNA compared with males (both P < .01). Unlike previously described for males, the presence of CMV DNA was not associated with increased HIV DNA in females. Among female participants, premenopausal status was independently associated with lower HIV DNA compared with postmenopause, after adjusting for nadir CD4 count (P < .01). Conclusions Female participants with HIV had reduced cellular HIV RNA and less subclinical CMV DNA compared with males but overall similar HIV DNA levels in our study. Postmenopausal status was independently associated with higher HIV DNA levels among female participants.

Funder

U.S. Department of Veterans Affairs

National Institutes of Health

The James B. Pendleton Charitable Trust

California HIV/AIDS Research Program

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Oncology

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