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"Air That Once Was Breath" Part 1: Wildfire-Smoke-Induced Mechanisms of Airway Inflammation - "Climate Change, Allergy and Immunology" Special IAAI Article Collection: Collegium Internationale Allergologicum Update 2023.
Bowman, Willis S; Schmidt, Rebecca J; Sanghar, Gursharan K; Thompson Iii, George R; Ji, Hong; Zeki, Amir A; Haczku, Angela.
Afiliação
  • Bowman WS; UC Davis Lung Center, University of California, Davis, California, USA.
  • Schmidt RJ; Division of Pulmonary, Critical Care, and Sleep Medicine, Department of Medicine, School of Medicine, Sacramento, California, USA.
  • Sanghar GK; Department of Public Health Sciences, School of Medicine, Sacramento, California, USA.
  • Thompson Iii GR; UC Davis Lung Center, University of California, Davis, California, USA.
  • Ji H; Division of Pulmonary, Critical Care, and Sleep Medicine, Department of Medicine, School of Medicine, Sacramento, California, USA.
  • Zeki AA; UC Davis Lung Center, University of California, Davis, California, USA.
  • Haczku A; Division of Infectious Diseases, Department of Medicine, School of Medicine, Sacramento, California, USA.
Int Arch Allergy Immunol ; 185(6): 600-616, 2024.
Article em En | MEDLINE | ID: mdl-38452750
ABSTRACT

BACKGROUND:

Wildfires are a global concern due to their wide-ranging environmental, economic, and public health impacts. Climate change contributes to an increase in the frequency and intensity of wildfires making smoke exposure a more significant and recurring health concern for individuals with airway diseases. Some of the most prominent effects of wildfire smoke exposure are asthma exacerbations and allergic airway sensitization. Likely due to the delayed recognition of its health impacts in comparison with cigarette smoke and industrial or traffic-related air pollution, research on the composition, the mechanisms of toxicity, and the cellular/molecular pathways involved is poor or non-existent.

SUMMARY:

This review discusses potential underlying pathological mechanisms of wildfire-smoke-related allergic airway disease and asthma. We focused on major gaps in understanding the role of wildfire smoke composition in the development of airway disease and the known and potential mechanisms involving cellular and molecular players of oxidative injury at the epithelial barrier in airway inflammation. We examine how PM2.5, VOCs, O3, endotoxin, microbes, and toxic gases may affect oxidative stress and inflammation in the respiratory mucosal barrier. We discuss the role of AhR in mediating smoke's effects in alarmin release and IL-17A production and how glucocorticoid responsiveness may be impaired by IL-17A-induced signaling and epigenetic changes leading to steroid-resistant severe airway inflammation. KEY MESSAGE Effective mitigation of wildfire-smoke-related respiratory health effects would require comprehensive research efforts aimed at a better understanding of the immune regulatory effects of wildfire smoke in respiratory health and disease.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fumaça / Mudança Climática / Incêndios Florestais Limite: Animals / Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fumaça / Mudança Climática / Incêndios Florestais Limite: Animals / Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article