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Inhibition of Toll-Like Receptor Signaling as a Promising Therapy for Inflammatory Diseases: A Journey from Molecular to Nano Therapeutics

2017· review· en· 351 citations· W2737868829 on OpenAlex· 10.3389/fphys.2017.00508

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Opus teacher head0.034
GPT teacher head0.313
Teacher spread
0.280 · how far apart the two teachers sit on this one work
Validation status
score_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Abstract

The recognition of invading pathogens and endogenous molecules from damaged tissues by toll-like receptors (TLRs) triggers protective self-defense mechanisms. However, excessive TLR activation disrupts the immune homeostasis by sustained pro-inflammatory cytokines and chemokines production and consequently contributes to the development of many inflammatory and autoimmune diseases, such as systemic lupus erythematosus (SLE), infection-associated sepsis, atherosclerosis, and asthma. Therefore, inhibitors/antagonists targeting TLR signals may be beneficial to treat these disorders. In this article, we first briefly summarize the pathophysiological role of TLRs in the inflammatory diseases. We then focus on reviewing the current knowledge in both preclinical and clinical studies of various TLR antagonists/inhibitors for the prevention and treatment of inflammatory diseases. These compounds range from conventional small molecules to therapeutic biologics and nanodevices. In particular, nanodevices are emerging as a new class of potent TLR inhibitors for their unique properties in desired bio-distribution, sustained circulation, and preferred pharmacodynamic and pharmacokinetic profiles. More interestingly, the inhibitory activity of these nanodevices can be regulated through precise nano-functionalization, making them the next generation therapeutics or "nano-drugs." Although, significant efforts have been made in developing different kinds of new TLR inhibitors/antagonists, only limited numbers of them have undergone clinical trials, and none have been approved for clinical uses to date. Nevertheless, these findings and continuous studies of TLR inhibition highlight the pharmacological regulation of TLR signaling, especially on multiple TLR pathways, as future promising therapeutic strategy for various inflammatory and autoimmune diseases.

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The record

Venue
Frontiers in Physiology
Topic
Immune Response and Inflammation
Field
Immunology and Microbiology
Canadian institutions
Funders
Shanghai General HospitalCrohn's and Colitis Foundation of CanadaProgram for Professor of Special Appointment (Eastern Scholar) at Shanghai Institutions of Higher LearningNational Natural Science Foundation of ChinaCrohn's and Colitis Foundation
Keywords
Toll-like receptorReceptorMedicineInflammationSignal transductionBioinformaticsPharmacologyComputational biologyImmunologyBiologyCell biologyInternal medicineInnate immune system
Has abstract in OpenAlex
yes