Impact of hormonal therapy on HIV‐1 immune markers in cis women and gender minorities

Author:

Pasin Chloé123ORCID,Nuñez David Garcia4,Kusejko Katharina12ORCID,Hachfeld Anna5ORCID,Buvelot Hélène6,Cavassini Matthias7ORCID,Damonti Lauro58ORCID,Fux Christoph9,de Tejada Begoña Martinez10ORCID,Notter Julia11ORCID,Trkola Alexandra2ORCID,Günthard Huldrych F.12ORCID,Aebi‐Popp Karoline5ORCID,Kouyos Roger D.12ORCID,Abela Irene A.12ORCID,

Affiliation:

1. Department of Infectious Diseases and Hospital Epidemiology University Hospital Zurich, University of Zurich Zurich Switzerland

2. Institute of Medical Virology University of Zurich Zurich Switzerland

3. Collegium Helveticum Zurich Switzerland

4. Center for Gender Variance, Department of Plastic, Reconstructive, Aesthetic and Hand Surgery University Hospital Basel Basel Switzerland

5. Department of Infectious Diseases University Hospital Bern Bern Switzerland

6. Division of Infectious Diseases Geneva University Hospitals Geneva Switzerland

7. Division of Infectious Diseases Lausanne University Hospital Lausanne Switzerland

8. Ente Ospedaliero Cantonale, Division of Infectious Diseases Regional Hospital Lugano Lugano Switzerland

9. Department of Infectious Diseases and Hospital Hygiene Kantonsspital Aarau Aarau Switzerland

10. Department of Pediatrics, Gynecology and Obstetrics University Hospitals of Geneva and Faculty of Medicine Geneva Switzerland

11. Division of Infectious Diseases and Hospital Epidemiology Cantonal Hospital St. Gallen St. Gallen Switzerland

Abstract

AbstractBackgroundAlthough sex hormones are recognized to induce immune variations, the effect of hormonal therapy use on immunity is only poorly understood. Here, we quantified how hormonal therapy use affects HIV‐1 immune markers in cis women (CW) and trans women and non‐binary people (TNBP) with HIV.MethodsWe considered CD4, CD8 and lymphocyte measurements from cis men (CM), CW and TNBP in the Swiss HIV Cohort Study. We modelled HIV‐1 markers using linear mixed‐effects models with an interaction between ‘gender’ (CW, TNBP) and ‘hormonal therapy use’ (yes/no). Models were adjusted on age, ethnicity, education level, time since start of antiretroviral therapy and use of intravenous drugs. We assessed the inflammatory effect of hormonal therapy use in 31 TNBP using serum proteomics measurements of 92 inflammation markers.ResultsWe included 54 083 measurements from 3092 CW and 83 TNBP, and 147 230 measurements from 8611 CM. Hormonal therapy use increased CD4 count and CD4:CD8 ratio in TNBP more than in CW (pinteraction = 0.02 and 0.007, respectively). TNBP with hormonal therapy use had significantly higher CD4 counts [median = 772 cells/μL, interquartile range (IQR): 520–1006] than without (617 cells/μL, 426–892). This was similar to the effect of CW versus CM on CD4 T cells. Hormonal therapy use did not affect serum protein concentrations in TNBP.ConclusionThis study highlights the potential role of hormonal therapy use in modulating the immune system among other biological and social factors, especially in TNBP with HIV.

Funder

Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung

Publisher

Wiley

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