| Literature DB >> 33912161 |
Jintao Zhang1,2, Chunyuan Zhao1,2,3, Wei Zhao1,2.
Abstract
The global expansion of coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has emerged as one of the greatest public health challenges and imposes a great threat to human health. Innate immunity plays vital roles in eliminating viruses through initiating type I interferons (IFNs)-dependent antiviral responses and inducing inflammation. Therefore, optimal activation of innate immunity and balanced type I IFN responses and inflammation are beneficial for efficient elimination of invading viruses. However, SARS-CoV-2 manipulates the host's innate immune system by multiple mechanisms, leading to aberrant type I IFN responses and excessive inflammation. In this review, we will emphasize the recent advances in the understanding of the crosstalk between host innate immunity and SARS-CoV-2 to explain the imbalance between inflammation and type I IFN responses caused by viral infection, and explore potential therapeutic targets for COVID-19.Entities:
Keywords: COVID-19; SARS-CoV-2; inflammation; innate immunity; type I interferons
Year: 2021 PMID: 33912161 PMCID: PMC8071932 DOI: 10.3389/fimmu.2021.633769
Source DB: PubMed Journal: Front Immunol ISSN: 1664-3224 Impact factor: 7.561