17β-Estradiol Dysregulates Innate Immune Responses to Pseudomonas aeruginosa Respiratory Infection and Is Modulated by Estrogen Receptor Antagonism

Author:

Abid Shadaan1,Xie ShangKui1,Bose Moumita1,Shaul Philip W.2,Terada Lance S.1,Brody Steven L.3,Thomas Philip J.4,Katzenellenbogen John A.5,Kim Sung Hoon5,Greenberg David E.1,Jain Raksha1

Affiliation:

1. Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, Texas, USA

2. Department of Pediatrics, University of Texas Southwestern Medical Center, Dallas, Texas, USA

3. Department of Internal Medicine, Washington University School of Medicine, St. Louis, Missouri, USA

4. Department of Physiology, University of Texas Southwestern Medical Center, Dallas, Texas, USA

5. Department of Chemistry, University of Illinois at Urbana—Champaign, Urbana, Illinois, USA

Abstract

ABSTRACT Females have a more severe clinical course than males in terms of several inflammatory lung conditions. Notably, females with cystic fibrosis (CF) suffer worse outcomes, particularly in the setting of Pseudomonas aeruginosa infection. Sex hormones have been implicated in experimental and clinical studies; however, immune mechanisms responsible for this sex-based disparity are unknown and the specific sex hormone target for therapeutic manipulation has not been identified. The objective of this study was to assess mechanisms behind the impact of female sex hormones on host immune responses to P. aeruginosa . We used wild-type and CF mice, which we hormone manipulated, inoculated with P. aeruginosa , and then examined for outcomes and inflammatory responses. Neutrophils isolated from mice and human subjects were tested for responses to P. aeruginosa . We found that female mice inoculated with P. aeruginosa died earlier and showed slower bacterial clearance than males ( P < 0.0001). Ovariectomized females supplemented with 17β-estradiol succumbed to P. aeruginosa challenge earlier than progesterone- or vehicle-supplemented mice ( P = 0.0003). 17β-Estradiol-treated ovariectomized female mice demonstrated increased lung levels of inflammatory cytokines, and when rendered neutropenic the mortality difference was abrogated. Neutrophils treated with 17β-estradiol demonstrated an enhanced oxidative burst but decreased P. aeruginosa killing and earlier cell necrosis. The estrogen receptor (ER) antagonist ICI 182,780 improved survival in female mice infected with P. aeruginosa and restored neutrophil function. We concluded that ER antagonism rescues estrogen-mediated neutrophil dysfunction and improves survival in response to P. aeruginosa . ER-mediated processes may explain the sex-based mortality gap in CF and other inflammatory lung illnesses, and the ER blockade represents a rational therapeutic strategy.

Funder

Childrens Medical Center - Dallas

HHS | National Institutes of Health

Gilead Sciences

Cystic Fibrosis Foundation

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Immunology,Microbiology,Parasitology

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