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EDITORIAL article

Front. Pharmacol., 14 January 2025
Sec. Respiratory Pharmacology
This article is part of the Research Topic Methods in Respiratory Pharmacology 2023 View all 5 articles

Editorial: Methods in respiratory pharmacology 2023

  • 1Department of Medicine, McMaster University, Hamilton, ON, Canada
  • 2Department of Life Sciences and Biotechnology, University of Ferrara, Ferrara, Italy
  • 3Department of Clinical Pharmacology and Therapeutics, Faculty of Medicine and Surgery, University of Malta, Msida, Malta

Editorial on the Research Topic
Methods in respiratory pharmacology 2023

It is our great pleasure to introduce the Research Topic “Methods in Respiratory Pharmacology 2023,” featured in this Research Topic of Frontiers in Pharmacology. This Research Topic underscores innovative methodologies, reflecting advancements that shape our understanding and treatment of respiratory diseases.

Respiratory pharmacology has significantly transformed with the development of sophisticated in vitro models and novel therapeutic strategies. This Research Topic encapsulates these advancements, providing valuable insights into experimental models and potential therapeutic agents that hold promise for improving patient outcomes.

One of the key contributions to this Research Topic is the article “3D Cell Culture Models in Research: Applications to Lung Cancer Pharmacology.” Lung cancer remains one of the leading causes of cancer-related mortality worldwide, necessitating innovative research methodologies to improve treatment outcomes. The advent of 3D cell culture techniques has marked a significant advancement in lung cancer research, offering more physiologically relevant models compared to traditional 2D cultures. These 3D models, including spheroids, organoids, and engineered tissue models, play pivotal roles in enhancing our understanding of lung cancer biology, facilitating drug development, and advancing precision medicine. By more closely mirroring human lung tumors, these models pave the way for more effective and personalized therapeutic strategies (Vella et al.).

Another notable manuscript is “A Novel In Vitro Cell Model of the Proteinase/Antiproteinase Balance Observed in Alpha-1 Antitrypsin Deficiency.” Alpha-1 antitrypsin deficiency (AATD) is a genetic condition that disrupts the proteinase/antiproteinase balance, leading to emphysema. Predicting and assessing human responses to therapeutic candidates from preclinical animal studies have been challenging. This study developed a physiologically relevant in vitro model of the proteinase/antiproteinase balance and assessed its predictive power for pharmacological efficacy. The results support an inhibitor threshold above which the activity footprint generation appears resistant to increasing dosage, helping test inhibitors and assess NSP activity in emphysema (Chen et al.).

The issue also includes a significant clinical study titled “The Use of Antibiotics in the Early Stage of Acute Exacerbation of Chronic Obstructive Pulmonary Disease (AECOPD) in Patients Without Obvious Signs of Infection: A Multicenter, Randomized, Parallel Controlled Study.” The use of antibiotics in the early stage of AECOPD in patients without obvious signs of infection is a contentious issue. This multicenter, randomized, parallel controlled study sought to clarify whether this treatment method, in the absence of clear infections indicators, has an impact on short- and long-term prognosis of AECOPD patients. The study found that while overall rates of exacerbation frequency, ICU treatment, and mortality were not significantly different between the antibiotic and nonantibiotic groups, the 30-day readmission rate was lower in the antibiotic group. Additionally, patients in the antibiotic group had shorter hospital stays and lower CRP levels and sputum viscosity at the 30-day follow-up, suggesting that antibiotics may improve short-term outcomes in specific subsets of AECOPD patients (Zhou et al.).

Lastly, the article “Vandetanib as a Prospective Anti-inflammatory and Anti-contractile Agent in Asthma” explores the therapeutic potential of vandetanib, a tyrosine kinase inhibitor, in treating asthma. Vandetanib, a tyrosine kinase inhibitor, primarily exerts therapeutic effects in lung cancers, but its potential benefits in asthma were unclear. This study investigated vandetanib’s anticontractile and anti-inflammatory properties in asthma, where in vivo experiments in an asthmatic mouse model showed that vandetanib alleviates systemic inflammation and various airway pathological changes, including hypersensitivity, hypersecretion, and remodeling. In vitro experiments demonstrated that vandetanib relaxes precontracted tracheal rings via calcium mobilization regulated by specific ion channels. These findings suggest the feasibility of using vandetanib to reduce abnormal airway contraction and systemic inflammation in asthma (Zeng et al.).

The contributions to this Research Topic underscore the dynamic and interdisciplinary nature of respiratory pharmacology. They reflect ongoing efforts to develop more effective treatments for respiratory diseases through innovative research and collaborative endeavors. We extend our gratitude to all authors and reviewers for their invaluable contributions and insights.

As editors, we are excited to share these advancements with the scientific community and hope this Research Topic inspires further research and innovation in respiratory pharmacology. We invite you to explore these articles and engage with the groundbreaking work presented in this Research Topic.

Author contributions

NM: Writing–original draft, Writing–review and editing. GC: Writing–original draft, Writing–review and editing. MC: Writing–original draft, Writing–review and editing.

Funding

The author(s) declare that no financial support was received for the research, authorship, and/or publication of this article.

Conflict of interest

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.

Generative AI statement

The author(s) declare that no Generative AI was used in the creation of this manuscript.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Keywords: respiratory disease, methodology, pharmacology, therapeutics, editorial

Citation: Milad N, Cabrini G and Cordina M (2025) Editorial: Methods in respiratory pharmacology 2023. Front. Pharmacol. 16:1527053. doi: 10.3389/fphar.2025.1527053

Received: 12 November 2024; Accepted: 06 January 2025;
Published: 14 January 2025.

Edited and reviewed by:

Paolo Montuschi, Catholic University of the Sacred Heart, Italy

Copyright © 2025 Milad, Cabrini and Cordina. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Nadia Milad, bWlsYWRuMUBtY21hc3Rlci5jYQ==

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.