Feminising hormone therapy reduces testicular ACE-2 receptor expression: Implications for treatment or prevention of COVID-19 infection in men. Academic Article uri icon

Overview

abstract

  • It has been proposed that men hospitalised with COVID-19 be treated with oestrogen or progesterone to improve COVID-19 outcomes. Transgender women (male-to-female) are routinely treated with oestrogen or oestrogen +progesterone for feminisation which provides a model for the effect of feminising hormones on testicular tissue. Our goal was to analyse differences in ACE-2 expression in testicles of trans-women taking oestrogen or oestrogen +progesterone. Orchiectomy specimens were collected from trans-women undergoing gender-affirming surgery, who were taking oestrogen or oestrogen+progesterone preoperatively. For controls, we used benign orchiectomy specimens from cis-gender men. All specimens were stained with H&E, Trichrome (fibrosis), insulin-like 3 antibody (Leydig cell) and ACE-2 IHC. Cells per high-powered field were counted by cell type (Leydig, Sertoli and Germ). Stain intensity was rated on a 0-2 scale. On immunohistochemistry staining for Leydig cells and ACE-2 staining, the oestrogen+progesterone cohort had fewer Leydig cells compared with controls. The oestrogen+progesterone cohort also had greater degree of tissue fibrosis compared with controls and the oestrogen cohort. This work supports the hopeful possibility that a short course of progesterone (or oestrogen+progesterone) could downregulate ACE-2 to protect men from COVID-19 infection.

authors

  • Masterson, John
  • Bui, Chau
  • Zhang, Yi
  • Yuan, Xiaopen
  • Huynh, Carissa
  • Jawanda, Harneet
  • Hasan, Wohaib
  • Tourtellotte, Warren
  • Luthringer, Daniel
  • Garcia, Maurice M

publication date

  • September 13, 2021

Research

keywords

  • Angiotensin-Converting Enzyme 2
  • Estrogens

Identity

PubMed Central ID

  • PMC8646357

Scopus Document Identifier

  • 85114748658

Digital Object Identifier (DOI)

  • 10.1111/and.14186

PubMed ID

  • 34514615

Additional Document Info

volume

  • 53

issue

  • 11