The Role of Toll-Like Receptors (TLR) in Infection and Inflammation

Toll-like receptors (TLRs) represent a powerful system for the recognition and elimination of pathogen-associated molecular patterns (PAMPs) from bacteria, viruses, and other pathogens and damage-associated molecular patterns (DAMPs) released from dying cells. Typical PAMPs include bacterial cell wa...

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Bibliographic Details
Other Authors: Kircheis, Ralf (Editor), Planz, Oliver (Editor)
Format: Electronic Book Chapter
Language:English
Published: Basel MDPI - Multidisciplinary Digital Publishing Institute 2023
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Online Access:DOAB: download the publication
DOAB: description of the publication
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520 |a Toll-like receptors (TLRs) represent a powerful system for the recognition and elimination of pathogen-associated molecular patterns (PAMPs) from bacteria, viruses, and other pathogens and damage-associated molecular patterns (DAMPs) released from dying cells. Typical PAMPs include bacterial cell wall components, viral pathogens, or pathogenic nucleic acids, including viral RNA and DNA. Activation of TLRs leads to the production of proinflammatory cytokines and type I interferons which are important for the induction of the host immune response against bacterial and viral infections. However, dysregulation and overstimulation can be detrimental, leading to hyper-inflammation, sepsis, and loss of tissue integrity. The involvement of TLRs in inflammation and bacterial infection has been recognized for a long time. There is an increasing number of reports demonstrating the involvement of TLR activation in a variety of viral infections, associated with protective immunity, but also immune hyper activation and even viral replication. Recent data show the involvement of TLR activation in various acute respiratory viral infections, including SARS-CoV-2 and indicate an essential role in COVID-19 pathology. It aimed to gather newest data and hypotheses regarding molecular and cellular mechanisms of TLR triggering and activation and their downstream signaling pathways by viral infections, and their correlation to immunology and pathophysiology of the associated diseases, to facilitate translational research resulting in new targets for the treatment of viral infectious diseases including COVID-19. 
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653 |a COVID-19 
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653 |a compression force 
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653 |a AKT 
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653 |a TLR 
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653 |a sepsis 
653 |a septic shock 
653 |a TLR7 
653 |a TLR8 
653 |a 2'-O-ribose-methylation 
653 |a RNase T2 
653 |a immune activation 
653 |a CD14 
653 |a LPS 
653 |a hop 
653 |a TLR4 
653 |a oligonucleotide 
653 |a sncRNA 
653 |a endocytosis 
653 |a broad-spectrum 
653 |a antiviral agent 
653 |a nucleolin 
653 |a virus entry 
653 |a immunoregulation 
653 |a RNA therapeutics 
653 |a TLR7 (Toll-like receptor 7) 
653 |a MUC1 (Mucin 1) 
653 |a aluminum adjuvant 
653 |a tumor vaccine 
653 |a immunotherapy 
653 |a toll-like receptor-2 (TLR2) 
653 |a advanced glycation end products (AGEs) 
653 |a aquaporin-3 (AQP3) 
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653 |a n/a 
653 |a TLR4-RAGE crosstalk 
653 |a glucose 
653 |a lipopolysaccharide (LPS) 
653 |a inflammatory 
653 |a alveolar macrophages 
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