The Complex Immune Cell Composition and Cellular Interaction in the Alveolar Compartment of Patients with Acute Respiratory Distress Syndrome.

Am J Respir Cell Mol Biol

Amsterdam UMC Locatie AMC, Intensive Care, Amsterdam, North Holland, Netherlands;

Published: October 2024

AI Article Synopsis

  • ARDS is driven by inflammation causing damage to the alveolar-capillary barrier, leading to fluid accumulation in the lungs, but research on immune cell interactions in this context is still limited.
  • Recent advances in single cell analysis allow for better understanding of how various immune cells, particularly neutrophils and macrophages, interact in the alveolar space of ARDS patients.
  • Understanding the cellular composition and its link to clinical outcomes may reveal new therapeutic targets, improving management and treatment options for ARDS.

Article Abstract

Acute respiratory distress syndrome (ARDS) is characterized by protein rich edema due to alveolar-capillary barrier dysfunction caused by inflammatory processes. Currently, our understanding of the inflammatory response in patients with ARDS is mainly based on assessment of the systemic compartment and preclinical studies. Investigations into the intricate network of immune cells and their critical functions in the alveolar compartment remain limited. However, with recent improvements in single cell analyses, our comprehensive understanding of the interactions between immune cells in the lungs has improved. In this review, we summarize the current knowledge about the cellular composition and interactions of different immune cell types within the alveolar space of patients with ARDS. Neutrophils and macrophages are the predominant immune cells in the alveolar space of ARDS patients. Yet, all immune cells present, including lymphocytes, participate in complex interactions, coordinate recruitment, modulate the lifespan and control apoptosis through various signaling pathways. Moreover, the cellular composition of alveolar immune cells is associated with clinical outcomes of ARDS patients. In conclusion, this synthesis advances our understanding of ARDS immunology, emphasizing the crucial role of immune cells within the alveolar space. Associations between cellular composition and clinical outcomes highlight the significance of exploring distinct alveolar immune cell subsets. Such exploration holds promise for uncovering novel therapeutic targets in ARDS pathophysiology, presenting avenues for enhancing clinical management and treatment strategies for ARDS patients. This article is open access and distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives License 4.0 (http://creativecommons.org/licenses/by-nc-nd/4.0/).

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Source
http://dx.doi.org/10.1165/rcmb.2024-0176TRDOI Listing

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