Journal of Respiratory Medicine
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  • Mini Review   
  • J Respir Med 6: 209,

Unveiling Inflammatory Pathways in Acute Respiratory Distress Syndrome: Insights and Therapeutic Implications

Himender Makker*
Department of Microbiology, University of Hong Kong, Hong Kong
*Corresponding Author : Himender Makker, Department of Microbiology, University of Hong Kong, Hong Kong, Email: makker.h15@hotmail.com

Received Date: Mar 04, 2024 / Published Date: Mar 29, 2024

Abstract

Acute Respiratory Distress Syndrome (ARDS) is a life-threatening condition characterized by severe respiratory failure and widespread inflammation within the lungs. The dysregulated inflammatory response plays a central role in the pathogenesis of ARDS, contributing to alveolar damage, impaired gas exchange, and systemic complications. This abstract provides an overview of the key inflammatory pathways involved in ARDS and explores their therapeutic implications. The inflammatory cascade in ARDS is initiated by the release of pro-inflammatory cytokines, which recruit and activate immune cells, leading to further amplification of the inflammatory response. Endothelial dysfunction and disruption of the alveolar-capillary barrier ensue, resulting in pulmonary edema and hypoxemia. Targeting inflammatory pathways holds significant promise in the management of ARDS. Strategies such as anti-inflammatory agents, cytokine blockade, neutrophil-targeted therapies, and mesenchymal stem cell therapy aim to modulate the inflammatory response and mitigate lung injury. While challenges remain, understanding and targeting inflammatory pathways offer valuable insights for the development of novel therapeutic interventions to improve outcomes in ARDS patients.

Citation: Himender M (2024) Unveiling Inflammatory Pathways in AcuteRespiratory Distress Syndrome: Insights and Therapeutic Implications. J RespirMed 6: 199.

Copyright: © 2024 Himender M. This is an open-access article distributed underthe terms of the Creative Commons Attribution License, which permits unrestricteduse, distribution, and reproduction in any medium, provided the original author andsource are credited.

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