| Autor: |
Poole JA; Division of Allergy & Immunology, Department of Internal Medicine, University of Nebraska Medical Center, Omaha, Nebraska, United States., Thiele GM; Veterans Affairs Nebraska-Western Iowa Health Care System, Research Service, Omaha, Nebraska, United States.; Division of Rheumatology & Immunology, Department of Internal Medicine, University of Nebraska Medical Center, Omaha, Nebraska, United States., Ramler E; Division of Allergy & Immunology, Department of Internal Medicine, University of Nebraska Medical Center, Omaha, Nebraska, United States., Nelson AJ; Division of Allergy & Immunology, Department of Internal Medicine, University of Nebraska Medical Center, Omaha, Nebraska, United States., Duryee MJ; Veterans Affairs Nebraska-Western Iowa Health Care System, Research Service, Omaha, Nebraska, United States.; Division of Rheumatology & Immunology, Department of Internal Medicine, University of Nebraska Medical Center, Omaha, Nebraska, United States., Schwab AD; Division of Allergy & Immunology, Department of Internal Medicine, University of Nebraska Medical Center, Omaha, Nebraska, United States., Gleason A; Division of Allergy & Immunology, Department of Internal Medicine, University of Nebraska Medical Center, Omaha, Nebraska, United States., Hunter CD; Veterans Affairs Nebraska-Western Iowa Health Care System, Research Service, Omaha, Nebraska, United States.; Division of Rheumatology & Immunology, Department of Internal Medicine, University of Nebraska Medical Center, Omaha, Nebraska, United States., Gaurav R; Division of Allergy & Immunology, Department of Internal Medicine, University of Nebraska Medical Center, Omaha, Nebraska, United States., Wyatt TA; Veterans Affairs Nebraska-Western Iowa Health Care System, Research Service, Omaha, Nebraska, United States.; Department of Environmental, Agricultural & Occupational Health, College of Public Health, University of Nebraska Medical Center, Omaha, Nebraska, United States.; Division of Pulmonary Critical Care & Sleep, Department of Internal Medicine, University of Nebraska Medical Center, Omaha, Nebraska, United States., England BR; Veterans Affairs Nebraska-Western Iowa Health Care System, Research Service, Omaha, Nebraska, United States.; Division of Rheumatology & Immunology, Department of Internal Medicine, University of Nebraska Medical Center, Omaha, Nebraska, United States., Mikuls TR; Veterans Affairs Nebraska-Western Iowa Health Care System, Research Service, Omaha, Nebraska, United States.; Division of Rheumatology & Immunology, Department of Internal Medicine, University of Nebraska Medical Center, Omaha, Nebraska, United States. |
| Abstrakt: |
Respiratory-related diseases are a leading cause of death in rheumatoid arthritis (RA) and are disproportionately higher in men, which may be attributable to environmental risk factors. Animal studies have demonstrated potentiated autoimmunity, arthritis, and profibrotic/inflammatory lung disease with a combination of airborne exposures and collagen-induced arthritis (CIA). This study aimed to determine whether hormone-dependent differences explained these observations. Arthritis-prone male intact and castrated DBA/1J mice received intranasal inhalation of lipopolysaccharide (LPS) daily for 5 wk and CIA induction. Arthritis scores and serum pentraxin-2 levels were increased in castrated versus intact mice. In contrast, airway cell influx, lung tissue infiltrates, and lung levels of proinflammatory and profibrotic markers (C5a, IL-33, and matrix metalloproteinases) were reduced in castrated versus intact mice. CIA + LPS-induced lung histopathology changes and the expression of lung autoantigens including malondialdehyde acetaldehyde (MAA)- and citrulline (CIT)-modified proteins and vimentin were reduced in castrated animals. There were no differences in serum anti-MAA or anti-CIT protein antibody (ACPA) levels or serum pentraxin levels between groups. Testosterone replacement led to a reversal of several lung inflammatory/profibrotic endpoints noted earlier in castrated male CIA + LPS-treated mice with testosterone supplementation promoting neutrophil influx, MAA expression, and TNF-α, IL-6, and MMP-9. These findings imply that testosterone contributes to lung and arthritis inflammatory responses following CIA + LPS coexposure, but not to systemic autoantibody responses. The CIA + LPS model provides a paradigm for investigations focused on the mechanistic underpinnings for epidemiologic and phenotypic sex differences in RA-related lung disease. NEW & NOTEWORTHY Our study shows that testosterone acts as a key immunomodulatory hormone contributing to critical features of rheumatoid arthritis (RA)-associated lung disease in the setting of airborne endotoxin (lipopolysaccharide; LPS) exposures and concomitant arthritis induction in mice. The exaggerated airway inflammation observed following combined exposures in male mice was accompanied by increases in profibrotic mediators, netosis, and increased expression of lung autoantigens, all relevant to the pathogenesis of lung disease in arthritis. |
