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Toll-like Receptor Mediation in SARS-CoV-2: A Therapeutic Approach.
Manan, Abdul; Pirzada, Rameez Hassan; Haseeb, Muhammad; Choi, Sangdun.
  • Manan A; Department of Molecular Science and Technology, Ajou University, Suwon 16499, Korea.
  • Pirzada RH; Department of Molecular Science and Technology, Ajou University, Suwon 16499, Korea.
  • Haseeb M; Department of Molecular Science and Technology, Ajou University, Suwon 16499, Korea.
  • Choi S; S&K Therapeutics, Ajou University Campus Plaza 418, 199 Worldcup-ro, Yeongtong-gu, Suwon 16502, Korea.
Int J Mol Sci ; 23(18)2022 Sep 14.
Article in English | MEDLINE | ID: covidwho-2032990
ABSTRACT
The innate immune system facilitates defense mechanisms against pathogen invasion and cell damage. Toll-like receptors (TLRs) assist in the activation of the innate immune system by binding to pathogenic ligands. This leads to the generation of intracellular signaling cascades including the biosynthesis of molecular mediators. TLRs on cell membranes are adept at recognizing viral components. Viruses can modulate the innate immune response with the help of proteins and RNAs that downregulate or upregulate the expression of various TLRs. In the case of COVID-19, molecular modulators such as type 1 interferons interfere with signaling pathways in the host cells, leading to an inflammatory response. Coronaviruses are responsible for an enhanced immune signature of inflammatory chemokines and cytokines. TLRs have been employed as therapeutic agents in viral infections as numerous antiviral Food and Drug Administration-approved drugs are TLR agonists. This review highlights the therapeutic approaches associated with SARS-CoV-2 and the TLRs involved in COVID-19 infection.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Interferon Type I / COVID-19 Drug Treatment Limits: Humans Language: English Year: 2022 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Interferon Type I / COVID-19 Drug Treatment Limits: Humans Language: English Year: 2022 Document Type: Article