4.6 Article

N-Acetylcysteine as Adjuvant Therapy for COVID-19-A Perspective on the Current State of the Evidence

Journal

JOURNAL OF INFLAMMATION RESEARCH
Volume 14, Issue -, Pages 2993-3013

Publisher

DOVE MEDICAL PRESS LTD
DOI: 10.2147/JIR.S306849

Keywords

N-acetylcysteine; SARS-CoV-2; COVID-19; coronavirus; repurposing approved drugs; engineering nanoparticles; virus infected cells; respiratory viral diseases; antioxidant; glutathione; T lymphocytes; immune modulating activity; anti-inflammatory response; antiviral effect; clinical translation

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N-acetylcysteine, as a precursor of the important antioxidant glutathione, has shown potential as an adjunctive therapy in respiratory viral infections, including COVID-19. In vitro and in vivo studies have demonstrated its ability to increase antioxidant capacity, interfere with virus replication, and modulate the immune response, suggesting it may be a promising treatment option for severe cases of COVID-19.
The looming severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has caused a long-lasting pandemic of coronavirus disease 2019 (COVID-19) around the globe with substantial morbidity and mortality. N-acetylcysteine, being a nutraceutical precursor of an important antioxidant glutathione, can perform several biological functions in mammals and microbes. It has consequently garnered a growing interest as a potential adjunctive therapy for coronavirus disease. Here, we review evidence concerning the effects of N-acetylcysteine in respiratory viral infections based on currently available in vitro, in vivo, and human clinical investigations. The repurposing of a known drug such as N-acetylcysteine may significantly hasten the deployment of a novel approach for COVID19. Since the drug candidate has already been translated into the clinic for several decades, its established pharmacological properties and safety and side-effect profiles expedite pre clinical and clinical assessment for the treatment of COVID-19. In vitro data have depicted that N-acetylcysteine increases antioxidant capacity, interferes with virus replication, and suppresses expression of pro-inflammatory cytokines in cells infected with influenza viruses or respiratory syncytial virus. Furthermore, findings from in vivo studies have displayed that, by virtue of immune modulation and anti-inflammatory mechanism, N-acetylcysteine reduces the mortality rate in influenza-infected mice animal models. The promising in vitro and in vivo results have prompted the initiation of human subject research for the treatment of COVID-19, including severe pneumonia and acute respiratory distress syndrome. Albeit some evidence of benefits has been observed in clinical outcomes of patients, precision nanoparticle design of N-acetylcysteine may allow for greater therapeutic efficacy.

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