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Targeting Type 2 Inflammation and Epithelial Alarmins in Chronic Obstructive Pulmonary Disease: A Biologics Outlook.
Rabe, Klaus F; Rennard, Stephen; Martinez, Fernando J; Celli, Bartolome R; Singh, Dave; Papi, Alberto; Bafadhel, Mona; Heble, Jigna; Radwan, Amr; Soler, Xavier; Jacob Nara, Juby A; Deniz, Yamo; Rowe, Paul J.
Afiliación
  • Rabe KF; LungenClinic Grosshansdorf, Grosshansdorf, Germany.
  • Rennard S; Christian Albrechts University of Kiel, Kiel, Germany.
  • Martinez FJ; Airway Research Center North, German Center for Lung Research, Grosshansdorf, Germany.
  • Celli BR; Department of Internal Medicine, University of Nebraska Medical Center, Omaha, Nebraska.
  • Singh D; NewYork-Presbyterian Hospital/Weill Cornell Medical Center, New York, New York.
  • Papi A; Pulmonary and Critical Care Division, Brigham and Women's Hospital, Boston, Massachusetts.
  • Bafadhel M; Harvard Medical School, Boston, Massachusetts.
  • Heble J; Medicines Evaluation Unit, Manchester University National Health Service Foundation Trust, University of Manchester, Manchester, United Kingdom.
  • Radwan A; Respiratory Medicine, Department of Translational Medicine, University of Ferrara, Ferrara, Italy.
  • Soler X; School of Immunology and Microbial Sciences, Faculty of Life Sciences and Medicine, King's College London, London, United Kingdom.
  • Jacob Nara JA; Sanofi, Bridgewater, New Jersey; and.
  • Deniz Y; Regeneron Pharmaceuticals Inc., Tarrytown, New York.
  • Rowe PJ; Regeneron Pharmaceuticals Inc., Tarrytown, New York.
Am J Respir Crit Care Med ; 208(4): 395-405, 2023 08 15.
Article en En | MEDLINE | ID: mdl-37348121
Chronic obstructive pulmonary disease (COPD) is a complex, heterogeneous, progressive inflammatory airway disease associated with a significant impact on patients' lives, including morbidity and mortality, and significant healthcare costs. Current pharmacologic strategies, including first- and second-line therapies such as long-acting ß2-agonists, long-acting muscarinic antagonists, inhaled corticosteroids, phosphodiesterase-4 inhibitors, and macrolides, provide relief to patients with COPD. However, many patients remain symptomatic, with persistent symptoms and/or acute exacerbations and progressive lung function loss. Although neutrophilic inflammation is the most common type of inflammation in COPD, 20-40% of patients with COPD exhibit type 2 inflammation, with roles for CD4+ (cluster of differentiation 4) T-helper cell type 1 cells, type 2 innate lymphoid cells, eosinophils, and alternatively activated macrophages. On the basis of the current limitations of available therapies, a significant unmet need exists in COPD management, including the need for targeted therapies to address the underlying pathophysiology leading to disease progression, such as type 2 inflammation, as well as biomarkers to help select the patients who would most benefit from the new therapies. Significant progress is being made, with evolving understanding of the pathobiology of COPD leading to novel therapeutic targets including epithelial alarmins. In this review, we describe the current therapeutic landscape in COPD, discuss unmet treatment needs, review the current knowledge of type 2 inflammation and epithelial alarmins in COPD, explore potential biomarkers of type 2 inflammation in COPD, and finally provide a rationale for incorporating therapies targeting type 2 inflammation and epithelial alarmins in COPD. Video Abstract available online at www.atsjournals.org.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Productos Biológicos / Enfermedad Pulmonar Obstructiva Crónica Límite: Humans Idioma: En Revista: Am J Respir Crit Care Med Asunto de la revista: TERAPIA INTENSIVA Año: 2023 Tipo del documento: Article País de afiliación: Alemania Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Productos Biológicos / Enfermedad Pulmonar Obstructiva Crónica Límite: Humans Idioma: En Revista: Am J Respir Crit Care Med Asunto de la revista: TERAPIA INTENSIVA Año: 2023 Tipo del documento: Article País de afiliación: Alemania Pais de publicación: Estados Unidos