N-acetylcysteine in Severe COVID-19: The Possible Mechanism

AUTHORS

Md Jahidul Hasan ORCID 1 , *

1 Clinical Pharmacy Services, Department of Pharmacy, Square Hospitals Ltd., 18/F Bir Uttam Qazi Nuruzzaman Sarak, West Panthapath, Dhaka-1205, Bangladesh

How to Cite: Hasan M J. N-acetylcysteine in Severe COVID-19: The Possible Mechanism, Int J Infect. Online ahead of Print ; 7(4):e106361. doi: 10.5812/iji.106361.

ARTICLE INFORMATION

International Journal of Infection: 7 (4); e106361
Published Online: August 31, 2020
Article Type: Letter
Received: June 12, 2020
Revised: August 5, 2020
Accepted: August 23, 2020
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Copyright © 2020, International Journal of Infection. This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/) which permits copy and redistribute the material just in noncommercial usages, provided the original work is properly cited.

Dear Editor,

Coronavirus Disease 2019 (COVID-19) caused by Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2), a new beta coronavirus, was officially declared a global pandemic by the World Health Organization (WHO) on March 11, 2020, after coming under the spotlight through a pneumonia outbreak in Wuhan, China, first reported on December 30, 2019. As of June 2, 2020, 6,194,533 confirmed COVID-19 cases, and 376,320 associated deaths were reported worldwide (1). The clinical investigation of COVID-19 cases shows that patients with COVID-19 are admitted to hospitals with common viral pneumonia symptoms, mostly including fever, dry cough, fatigue, sore throat, and shortness of breath (2). Hyperinflammation-associated Acute Lung Injury (ALI) is the leading cause of death among patients with severe COVID-19, and highly expressed inflammatory cytokines, including interleukin (IL)-6, IL-10, IL-1β, and Tumour Necrosis Factor-α (TNF-α) play a pivotal role in aggravating the inflammatory responses (3, 4).

SARS-CoV-2 binds to the Angiotensin-Converting Enzyme-2 (ACE-2) receptor in human alveolar epithelial cells to enter the host cell; in response, the activated innate and adaptive immune systems of the host release a variety of pro-inflammatory cytokines, including IL-6, IL-10, TNF-α, and MIP-1-α, leading to a cytokine storm. In addition, the released chemokines activate the secretion of other inflammatory mediators from peripheral blood into the site of inflammation and potentiate the cytokine storm (Figure 1). Increased vascular permeability and fluid accumulation in alveoli is due to the activities of these pro-inflammatory cytokines, resulting in respiratory failure (3, 5).

Figure 1. Anti-inflammatory role N-acetylcysteine in patients with severe COVID-19; (a) Release of pro-inflammatory cytokines in direct response to SARS-CoV-2-host cell interaction; (b) Proliferation of intracellular oxidative stress due to the release of pro-inflammatory cytokines; (c) Inhibitory role of NAC in the extensive release of pro-inflammatory cytokines and chemokines; (d) Inhibitory role of NAC in the exacerbation of intracellular oxidative stress

The WHO declares N-acetylcysteine (NAC), a relevant medication intended to use in the basic health system, and it is generally used as a mucolytic, anti-inflammatory, and antioxidant agent (6). As an anti-inflammatory agent, NAC prevents the release of pro-inflammatory cytokines in the initial state of immune proliferation in disease progression, and this mechanism is based on the inhibition of the activities of lipopolysaccharides. Nuclear Factor-kappa B (NF-κB) plays a pivotal role in inflammation cascades, and the bonding between I-κB kinase (I-κB) and NF-κB prevents its nuclear translocation. IκB kinase β (IKKβ) regulates the separation of I-κB from NF-κB by phosphorylation (lipopolysaccharide-induced) and its degradation by the proteasome and allows NF-κB to enter into the nucleus where this transcription factor (NF-κB) activates the release of pro-inflammatory cytokines, mostly including IL-6, IL-1β, and TNF-α (6), which are also found in high levels in patients with severe COVID-19 (3, 4). NAC exhibits its sole anti-inflammatory characteristic by inhibiting the activation of NF-κB activities through the suppression of the activities of lipopolysaccharides (Figure 1). Multiple studies found high serum IL-6 levels in COVID-19 patients (3-5), and its release is significantly enhanced by the action of both IL-1β and TNF-α in early inflammation state. In effect, NAC inhibits the expression of IL-6 by significantly reducing the levels of IL-1β and TNF-α (3, 7, 8). Furthermore, in severe COVID-19 patients, high levels of IL-10 are detected (3, 5), which significantly contributes to immune proliferation. An in-vitro study showed that IL-10 mRNA expression was highly downregulated by NAC, resulting in the suppression of the proliferation of inflammation cascades (7, 8).

In its primary role, NAC is a precursor of glutathione (GSH) synthesis, which is the principal antioxidant that the body produces to protect its cells from serious injury or death due to high levels of Reactive Oxygen Species (ROS), resulting in intracellular oxidative stress (6). In addition, inflammation extensively accelerates the production of ROS, leading to massive oxidative stress at the site of inflammation (Figure 1). An increased level of TNF-α allows more ROS to generate in mitochondria, which significantly potentiates NF-κB to exacerbate the cytokine storm, leading to cell death (9) (Figure 1). In addition, in response to oxidative stress, lung epithelial cells predominantly release pro-inflammatory cytokines, including IL-6, IL-10, IL-1β, and TNF-α (Figure 1). NAC improves the cellular total antioxidant capacity through improving GSH concentration and directly interacts with ROS, including hydroxyl radicals, nitrogen dioxide, and carbon trioxide ion using its free thiol side-chain (8). Even at a low intracellular concentration, NAC replenishes the GSH level, resulting in a healthy intracellular environment (8, 9). The lower the level of intracellular oxidative stress, the higher the chance of overcoming pulmonary damage in severe COVID-19 infection (9). Thus, NAC inhibits the expression of pro-inflammatory cytokines, which may potentially suppress the progression of ALI in patients with severe COVID-19.

An extensive release of pro-inflammatory cytokines and excessive intracellular oxidative stress in a severe stage of COVID-19 causes massive cytokine storm that develops severe ALI, leading to respiratory failure (2-5). The multi-dimensional target-specific anti-inflammatory roles of NAC significantly suppress the release of IL-6, IL-10, IL-1β, and TNF-α, which are the most robust components of inflammation cascades, and the primary antioxidant property of NAC reduces the intensity of intracellular oxidative stress in severe COVID-19 (7-9). Therefore, NAC may be effective in the management of severe pulmonary inflammation in viral pneumonia, including COVID-19, and may reduce the risk of acute respiratory failure-associated mortality in patients with severe COVID-19.

Footnotes

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