The novel coronavirus (CoV) disease 2019 (COVID-19), which first appeared in Wuhan,
China, in December 2019, spreads efficiently from person to person. After it had reached
over 100 countries, on 11 March 2020 the WHO declared it a pandemic . COVID-19
is caused by SARS-CoV-2, and by 9 June 2020 had been responsible for 7,039,918 confirmed
cases and 404,396 deaths worldwide . At the time of writing, the five countries
with the highest number of cases are the USA (1,933,560 cases), Brazil (691,758 cases),
the Russian Federation (485,253 cases), the UK (287,403 cases) and India (266,598
The scientific community’s rapid response has allowed description of the complete
SARS-CoV-2 genome, which is currently available on bioinformatics platforms. Analysis
of the genome has found an 88% identity with two bat-derived SARS-like CoVs, bat-SL-CoVZC45
and bat-SL-CoVZXC21, both collected in 2018 in Zhoushan, Eastern China; it also has
approximately 79% identity with 2002 SARS-CoV . It is no surprise therefore that
SARS-CoV-2 shares host cell infection mechanisms with SARS-CoV. Angiotensin-converting
enzyme 2 (ACE2) has been shown to be the receptor in which the SARS-CoV-2 spike (S)
glycoprotein allows membrane fusion and internalization . The SARS-CoV-2 S glycoprotein
bonds to ACE2 resulting in reduced expression of the enzyme; this generates angiotensin
II accumulation generated by ACE. The depleted ACE2 is unable to convert angiotensin
I into the vasodilator heptapeptide angiotensin 1–7, thus generating pulmonary injury;
also, angiotensin II type-1 receptor overstimulation results in increased lung vascularity
which contributes to the overall pathology. Human ACE2 and the SARS-CoV-2 S glycoprotein
have consequently been identified as the therapeutic targets for development of new
treatments such as antivirals and monoclonal antibodies, or for identification of
existing drugs capable of blocking interaction between the virus and the host cell.
The SARS-CoV-2 S glycoprotein consists of two subunits, S1, which facilitates viral
bond to the host cell, and S2, which assists viral membrane fusion . The fusion
process depends on S glycoprotein cleavage at the S1/S2 multibasic site, mainly by
the human protease furin . In vitro results demonstrate the essential role of this
cleavage site to promote viral entrance into lung cells . Thus, direct inhibition
of furin or disruption of the interactions between the S1/S2 complex and this protease
are potential therapeutic approaches.
We propose N-acetylcysteine (NAC) as a potential treatment, preventive and/or adjuvant
against SARS-CoV-2. It has two principal activities: NAC exhibits a mucolytic effect
due to its free sulfhydryl group which reduces disulfide bonds in the cross-linked
mucus glycoproteins matrix, thereby lowering mucus viscosity ; and NAC is a potent
antioxidant with a direct effect on certain oxidant species, an indirect effect because
it acts as a precursor to cysteine (required for glutathione synthesis), and the ability
to restore thiol pools which in turn regulate redox state .
Considering these properties, we hypothesize that NAC could negatively affect SARS-CoV-2
activity for the following reasons:
The E protein of SARS-CoV (genetically related to SARS-CoV-2) consists of 76–109 amino
acids, ranging in size from 8.4 to 12 kDa. Its primary and secondary structures have
a short, hydrophilic amine terminus group of 7–12 amino acids followed by a hydrophobic
25 amino acid transmembrane domain which ends in a hydrophilic carboxyl group terminus
. The SARS-CoV-2 E protein includes a triple cysteine motif (NH2- … L-Cys-A-Y-Cys-Cys-N
… -COOH) after the transmembrane domain which interacts with a similar motif from
S protein terminal C- (NH2- … S-Cys-G-S-Cys-Cys-K … -COOH) . Both motifs interact
through disulfide bonds , and NAC may cleave them. This would decrease SARS-CoV-2
In vitro studies have shown NAC to decrease angiotensin II bonds to angiotensin II
type 1 receptor in a dose-dependent manner . In the COVID-19 context, NAC could
block excessive production of angiotensin II, which cannot be cleaved to angiotensin
1–7 by ACE2. This may decrease pulmonary disease severity.
In vitro and clinical studies have shown NAC to block ACE. In one experiment isosorbide
dinitrate (vasodilator activity) was administered to six male participants for 48 h,
but at 24 h NAC was added (2 g intravenously [iv.] followed by 5 mg/kg/h). Angiotensin
II plasma concentrations increased during the first 24 h of isosorbide dinitrate administration
but just 2 h after NAC initiation they had decreased from 28 ± 4 to 14 ± 2 ng/l (p
< 0.05) . This suggests that, by blocking ACE, NAC may provide protection from
the deleterious effects of angiotensin II, a potentially useful activity in a SARS-CoV-2
The oxidative stress environment created by cytokine storm syndrome and production
of reactive oxygen species (ROS) may be attenuated by NAC’s antioxidant effect .
Also, the SARS-CoV-2 immunopathology may be similar to that of SARS-CoV, which generates
an immune response involving diverse pro-inflammatory cytokines (IL-1, IL-2, IL-4,
TNF and IFNs). The IFNs are classified in type-I (IFN-α and β), -II (IFN-γ) and -III.
Type-I IFNs are suppressed during SARS-CoV infection due to impairment of signal transducer
and activator of transcription 1, which ultimately antagonizes IFN. This complex mechanism
may also generate delayed IFN response due to cytokine storm syndrome during SARS-CoV-2
infection, possibly explaining COVID-19 pathology. NAC may amplify the signaling functions
of toll-like receptor 7 and mitochondrial antiviral signaling protein in restoring
type-I IFN production during SARS-CoV-2 infection .
NAC has been shown to restore platelet GSH reserves (in a murine model) which in turn
can prevent protein glycosylation by methylglyoxal, a pathologic mechanism in diabetic
patients . The SARS-CoV-2 S glycoprotein differs from that of SARS-CoV in that
it gains new glycosylation sites (NGTK, NFTI, NLTT and NTSN), allowing SARS-CoV-2
to enter the host cell . Administration of NAC could prevent additional glycosylation
events in SARS-CoV-2, thus inhibiting its infectivity and any associated pathologies.
In a recent study the NF-κB was described as a mediator of SARS-CoV-2 pulmonary pathology
since it triggers the production of numerous pro-inflammatory cytokines. This process
generates macrophage and neutrophil infiltration, both of which cause irreparable
damage to pulmonary epithelium cells. NAC was shown to inhibit NF-κB activation in
an in vitro influenza (A and B) model ; the proposed mechanism is restauration
of thiol pools which may allow ROS scavenging. This is relevant because recent clinical
experience has shown that severity of COVID-19 clinical manifestations might be associated
with decreased GSH levels and the consequent increased ROS production. Severe COVID-19
cases would therefore probably manifest lower GSH levels, higher ROS levels and greater
redox status (ROS/GSH ratio) than milder cases .
In the context of influenza virus infection, NAC administration (100 mg/kg continuous
iv. infusion daily for 3 days) was reported to promote clinical improvement in a woman
with H1N1 influenza pneumonia; oseltamivir was also employed during treatment .
However, other studies have found no beneficial in vitro or vivo effects with NAC
administration . NAC (600 mg twice daily) has also been reported to attenuate
influenza symptoms in patients ≥65-years old with chronic-degenerative diseases .
Given this pandemic’s immense health risk, several drugs have been employed with and
without clinical evidence for the treatment of COVID-19, NAC among them . Administration
of NAC (oral, iv. or inhaled) as an adjuvant treatment in patients with mild–severe
COVID-19 symptoms is worth considering as a cost–effective clinical strategy. Currently,
there are some clinical trials assessing the potential use of NAC against COVID-19;
for example, the ‘Efficacy and Safety of Nebulized Heparin-N-acetylcysteine in COVID-19
Patients by Evaluation of Pulmonary Function Improvement (HOPE)’ clinical trial is
aimed at determining the efficacy of nebulized NAC and heparin in ventilated COVID-19
patients . The aim is to increase ventilator-free days in hospitalized patients
with moderate–severe COVID-19 symptoms. Another recent study is ‘A Study of N-acetylcysteine
in Patients With COVID-19 Infection’, a clinical trial aimed at quantifying: the number
of patients successfully extubated and/or transferred from critical care unit due
to clinical improvement; and the number of patients discharged due to clinical improvement.
Patients are receiving NAC iv. 6 g/day in addition to other treatments prescribed
for COVID-19 .
Oral administration of NAC (600 mg/day) could function as a preventive measure, particularly
in those repeatedly exposed to possible SARS-CoV-2 carriers (e.g., health workers).
This application could be a particularly urgent approach since, despite the use of
personal protective equipment, healthcare workers in the USA, Italy, China, Mexico,
etc., have become infected while caring for hospitalized patient. Other workers who,
due to their job requirements, cannot work at home and/or ensure self-isolation might
also benefit from preventive use of NAC administration. If deemed effective, this
latter use could potentially help to flatten the exponential contagion curve in several
countries. More clinical trials would clearly be needed to validate this application.
Basic laboratory and clinical studies are required to confirm possible use of NAC
as an element in combating the disease caused by SARS-CoV-2. This would need to be
one of myriad efforts to identify additional treatments (novel or not) aimed at halting
the current COVID-19 pandemic, or at the very least slowing person-to-person contagion.