Unraveling the Complexities of Toll-like Receptors: From Molecular Mechanisms to Clinical Applications

Author:

Chen Yi-Hsin123ORCID,Wu Kang-Hsi45,Wu Han-Ping67ORCID

Affiliation:

1. Department of Nephrology, Taichung Tzu Chi Hospital, Taichung 427, Taiwan

2. School of Medicine, Tzu Chi University, Hualien 97004, Taiwan

3. Department of Artificial Intelligence and Data Science, National Chung Hsing University, Taichung 40227, Taiwan

4. Department of Pediatrics, Chung Shan Medical University Hospital, Taichung 402, Taiwan

5. School of Medicine, Chung Shan Medical University, Taichung 402, Taiwan

6. College of Medicine, Chang Gung University, Taoyuan 33302, Taiwan

7. Department of Pediatrics, Chiayi Chang Gung Memorial Hospital, Chiayi 613016, Taiwan

Abstract

Toll-like receptors (TLRs) are vital components of the innate immune system, serving as the first line of defense against pathogens by recognizing a wide array of molecular patterns. This review summarizes the critical roles of TLRs in immune surveillance and disease pathogenesis, focusing on their structure, signaling pathways, and implications in various disorders. We discuss the molecular intricacies of TLRs, including their ligand specificity, signaling cascades, and the functional consequences of their activation. The involvement of TLRs in infectious diseases, autoimmunity, chronic inflammation, and cancer is explored, highlighting their potential as therapeutic targets. We also examine recent advancements in TLR research, such as the development of specific agonists and antagonists, and their application in immunotherapy and vaccine development. Furthermore, we address the challenges and controversies surrounding TLR research and outline future directions, including the integration of computational modeling and personalized medicine approaches. In conclusion, TLRs represent a promising frontier in medical research, with the potential to significantly impact the development of novel therapeutic strategies for a wide range of diseases.

Publisher

MDPI AG

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