Alveolar macrophages in lung cancer: opportunities challenges.

immune checkpoint inhibitors lung cancer smoking tissue-resident alveolar macrophages tumor microenvironment tumor-associated macrophages

Journal

Frontiers in immunology
ISSN: 1664-3224
Titre abrégé: Front Immunol
Pays: Switzerland
ID NLM: 101560960

Informations de publication

Date de publication:
2023
Historique:
received: 28 07 2023
accepted: 12 09 2023
medline: 1 11 2023
pubmed: 12 10 2023
entrez: 12 10 2023
Statut: epublish

Résumé

Alveolar macrophages (AMs) are critical components of the innate defense mechanism in the lung. Nestled tightly within the alveoli, AMs, derived from the yolk-sac or bone marrow, can phagocytose foreign particles, defend the host against pathogens, recycle surfactant, and promptly respond to inhaled noxious stimuli. The behavior of AMs is tightly dependent on the environmental cues whereby infection, chronic inflammation, and associated metabolic changes can repolarize their effector functions in the lungs. Several factors within the tumor microenvironment can re-educate AMs, resulting in tumor growth, and reducing immune checkpoint inhibitors (ICIs) efficacy in patients treated for non-small cell lung cancer (NSCLC). The plasticity of AMs and their critical function in altering tumor responses to ICIs make them a desirable target in lung cancer treatment. New strategies have been developed to target AMs in solid tumors reprograming their suppressive function and boosting the efficacy of ICIs. Here, we review the phenotypic and functional changes in AMs in response to sterile inflammation and in NSCLC that could be critical in tumor growth and metastasis. Opportunities in altering AMs' function include harnessing their potential function in trained immunity, a concept borrowed from memory response to infections, which could be explored therapeutically in managing lung cancer treatment.

Identifiants

pubmed: 37822933
doi: 10.3389/fimmu.2023.1268939
pmc: PMC10562548
doi:

Types de publication

Journal Article Review Research Support, N.I.H., Extramural Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

1268939

Subventions

Organisme : NHLBI NIH HHS
ID : R01 HL140398
Pays : United States
Organisme : BLRD VA
ID : I01 BX004828
Pays : United States
Organisme : CSRD VA
ID : I01 CX000104
Pays : United States
Organisme : NIEHS NIH HHS
ID : R01 ES029442
Pays : United States
Organisme : NIAID NIH HHS
ID : R41 AI164997
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL117181
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI135803
Pays : United States

Commentaires et corrections

Type : ErratumIn

Informations de copyright

Copyright © 2023 Chang, Armstrong, Corry and Kheradmand.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Cheng-Yen Chang (CY)

Department of Medicine, Baylor College of Medicine, Houston, TX, United States.

Dominique Armstrong (D)

Department of Medicine, Baylor College of Medicine, Houston, TX, United States.

David B Corry (DB)

Department of Medicine, Baylor College of Medicine, Houston, TX, United States.
Department of Pathology and Immunology, Baylor College of Medicine, Houston, TX, United States.
Biology of Inflammation Center, Baylor College of Medicine, Houston, TX, United States.
Center for Translational Research on Inflammatory Diseases, Michael E. DeBakey Department of Veterans Affairs Medical Center, Houston, TX, United States.

Farrah Kheradmand (F)

Department of Medicine, Baylor College of Medicine, Houston, TX, United States.
Department of Pathology and Immunology, Baylor College of Medicine, Houston, TX, United States.
Biology of Inflammation Center, Baylor College of Medicine, Houston, TX, United States.
Center for Translational Research on Inflammatory Diseases, Michael E. DeBakey Department of Veterans Affairs Medical Center, Houston, TX, United States.

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