@article{fa8422c7c6544d618ac5adc2a092fac9,
title = "Targeting eosinophils in respiratory diseases: Biological axis, emerging therapeutics and treatment modalities",
abstract = "Eosinophils are bi-lobed, multi-functional innate immune cells with diverse cell surface receptors that regulate local immune and inflammatory responses. Several inflammatory and infectious diseases are triggered with their build up in the blood and tissues. The mobilization of eosinophils into the lungs is regulated by a cascade of processes guided by Th2 cytokine generating T-cells. Recruitment of eosinophils essentially leads to a characteristic immune response followed by airway hyperresponsiveness and remodeling, which are hallmarks of chronic respiratory diseases. By analysing the dynamic interactions of eosinophils with their extracellular environment, which also involve signaling molecules and tissues, various therapies have been invented and developed to target respiratory diseases. Having entered clinical testing, several eosinophil targeting therapeutic agents have shown much promise and have further bridged the gap between theory and practice. Moreover, researchers now have a clearer understanding of the roles and mechanisms of eosinophils. These factors have successfully assisted molecular biologists to block specific pathways in the growth, migration and activation of eosinophils. The primary purpose of this review is to provide an overview of the eosinophil biology with a special emphasis on potential pharmacotherapeutic targets. The review also summarizes promising eosinophil-targeting agents, along with their mechanisms and rationale for use, including those in developmental pipeline, in clinical trials, or approved for other respiratory disorders.",
keywords = "Respiratory diseases, Pulmonary, Eosinophils, Targeted therapies, Immunity, Lung, Lung/metabolism, Eosinophils/drug effects, Humans, Cytokines/immunology, Th2 Cells/immunology, Animals, Respiration Disorders/immunology, Respiratory Tract Diseases/immunology",
author = "Li-yen Lee and Hew, \{Geena Suet Yin\} and Meenu Mehta and Shukla, \{Shakti D.\} and Saurabh Satija and Navneet Khurana and Krishnan Anand and Harish Dureja and Singh, \{Sachin Kumar\} and Vijay Mishra and Singh, \{Pankaj Kumar\} and Monica Gulati and Parteek Prasher and Aljabali, \{Alaa A.a.\} and Tambuwala, \{Murtaza M.\} and Lakshmi Thangavelu and Jithendra Panneerselvam and Gaurav Gupta and Zacconi, \{Flavia C.\} and Madhur Shastri and Jha, \{Niraj Kumar\} and Dikaia Xenaki and Ronan Macloughlin and Oliver, \{Brian G.\} and Chellappan, \{Dinesh Kumar\} and Kamal Dua",
note = "Funding Information: The authors would like to thank the School of Pharmacy , International Medical University , Kuala Lumpur, Malaysia and the Graduate School of Health , University of Technology Sydney , Australia. Kamal Dua is supported by a project grant from Rebecca L. Cooper Medical Research Foundation and Sydney Partnership for Health, Education, Research and Enterprise. Publisher Copyright: {\textcopyright} 2021 Elsevier Inc. Copyright: Copyright 2021 Elsevier B.V., All rights reserved.",
year = "2021",
month = feb,
day = "15",
doi = "10.1016/j.lfs.2020.118973",
language = "English",
volume = "267",
journal = "Life Sciences",
issn = "0024-3205",
publisher = "Elsevier Inc.",
}