| Literature DB >> 34160586 |
Milankumar Patel1, Farah Shahjin1, Jacob D Cohen1, Mahmudul Hasan2, Jatin Machhi1, Heerak Chugh3, Snigdha Singh3, Srijanee Das4, Tanmay A Kulkarni2, Jonathan Herskovitz1,4, Douglas D Meigs1, Ramesh Chandra3,5, Kenneth S Hettie6, R Lee Mosley1, Bhavesh D Kevadiya1, Howard E Gendelman1,2,4.
Abstract
Infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) can lead to coronavirus disease 2019 (COVID-19). Virus-specific immunity controls infection, transmission and disease severity. With respect to disease severity, a spectrum of clinical outcomes occur associated with age, genetics, comorbidities and immune responses in an infected person. Dysfunctions in innate and adaptive immunity commonly follow viral infection. These are heralded by altered innate mononuclear phagocyte differentiation, activation, intracellular killing and adaptive memory, effector, and regulatory T cell responses. All of such affect viral clearance and the progression of end-organ disease. Failures to produce effective controlled antiviral immunity leads to life-threatening end-organ disease that is typified by the acute respiratory distress syndrome. The most effective means to contain SARS-CoV-2 infection is by vaccination. While an arsenal of immunomodulators were developed for control of viral infection and subsequent COVID-19 disease, further research is required to enable therapeutic implementation.Entities:
Keywords: ACE2; COVID-19 vaccines; SARS-CoV-2; cytokine storm; immunity; mutant viral variants
Mesh:
Year: 2021 PMID: 34160586 PMCID: PMC8632753 DOI: 10.1093/femsre/fuab035
Source DB: PubMed Journal: FEMS Microbiol Rev ISSN: 0168-6445 Impact factor: 16.408