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Therapeutic Targeting of Innate Immune Receptors Against SARS-CoV-2 Infectionoa mark
  • Farooq, Mariya ;
  • Khan, Abdul Waheed ;
  • Ahmad, Bilal ;
  • Kim, Moon Suk ;
  • Choi, Sangdun
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Publication Year
2022-06-30
Publisher
Frontiers Media S.A.
Citation
Frontiers in Pharmacology, Vol.13
Keyword
antiviral responseinnate immune receptorRIG-like receptorSARS-CoV-2toll-like receptor
All Science Classification Codes (ASJC)
PharmacologyPharmacology (medical)
Abstract
The innate immune system is the first line of host’s defense against invading pathogens. Multiple cellular sensors that detect viral components can induce innate antiviral immune responses. As a result, interferons and pro-inflammatory cytokines are produced which help in the elimination of invading viruses. Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) belongs to Coronaviridae family, and has a single-stranded, positive-sense RNA genome. It can infect multiple hosts; in humans, it is responsible for the novel coronavirus disease 2019 (COVID-19). Successful, timely, and appropriate detection of SARS-CoV-2 can be very important for the early generation of the immune response. Several drugs that target the innate immune receptors as well as other signaling molecules generated during the innate immune response are currently being investigated in clinical trials. In this review, we summarized the current knowledge of the mechanisms underlying host sensing and innate immune responses against SARS-CoV-2 infection, as well as the role of innate immune receptors in terms of their therapeutic potential against SARS-CoV-2. Moreover, we discussed the drugs undergoing clinical trials and the FDA approved drugs against SARS-CoV-2. This review will help in understanding the interactions between SARS-CoV-2 and innate immune receptors and thus will point towards new dimensions for the development of new therapeutics, which can be beneficial in the current pandemic.
ISSN
1663-9812
Language
eng
URI
https://dspace.ajou.ac.kr/dev/handle/2018.oak/32809
DOI
https://doi.org/10.3389/fphar.2022.915565
Fulltext

Type
Review
Funding
This research was supported by South Korea Drug Development Fund funded by Ministry of Science and ICT, Ministry of Trade, Industry, and Energy, and Ministry of Health and Welfare (HN21C1058). This work was also supported by the National Research Foundation of Korea (NRF-2022M3A9G1014520, 2019M3D1A1078940 and 2019R1A6A1A11051471).
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