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      Nitric oxide (NO) and nanoparticles – potential small tools for the war against COVID-19 and other human coronavirus infections

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          Highlights

          • Nitric oxide has shown antiviral potential against respiratory viral infections.

          • Protocols of inhaled nitric oxide against COVID-19 are in current trial.

          • Current trials might indicate suitable parameters for nitric oxide treatment against COVID-19.

          • Nitric oxide allied to nanoparticles may improve the antiviral potential.

          Abstract

          The endogenous free radical nitric oxide (NO) plays a pivotal role in the immunological system. NO has already been reported as a potential candidate for use in the treatment of human coronavirus infections, including COVID-19. In fact, inhaled NO has been used in clinical settings for its antiviral respiratory action, and in the regulation of blood pressure to avoid clot formation. In this mini-review, we discuss recent progress concerning the antivirus activity of NO in clinical, pre-clinical and research settings, and its beneficial effects in the treatment of clinical complications in patients infected with coronaviruses and other respiratory viral diseases, including COVID-19. We also highlight promising therapeutic effects of NO donors allied to nanomaterials to combat COVID-19 and other human coronavirus infections. Nanomaterials can be designed to deliver sustained, localized NO release directly at the desired application site, enhancing the beneficial effects of NO and minimizing the side effects. Challenges and perspectives are presented to open new fields of research.

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          Most cited references64

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          Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and coronavirus disease-2019 (COVID-19): The epidemic and the challenges

          Highlights • Emergence of 2019 novel coronavirus (2019-nCoV) in China has caused a large global outbreak and major public health issue. • At 9 February 2020, data from the WHO has shown >37 000 confirmed cases in 28 countries (>99% of cases detected in China). • 2019-nCoV is spread by human-to-human transmission via droplets or direct contact. • Infection estimated to have an incubation period of 2–14 days and a basic reproduction number of 2.24–3.58. • Controlling infection to prevent spread of the 2019-nCoV is the primary intervention being used.
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            IDO expression by dendritic cells: tolerance and tryptophan catabolism.

            Indoleamine 2,3-dioxygenase (IDO) is an enzyme that degrades the essential amino acid tryptophan. The concept that cells expressing IDO can suppress T-cell responses and promote tolerance is a relatively new paradigm in immunology. Considerable evidence now supports this hypothesis, including studies of mammalian pregnancy, tumour resistance, chronic infections and autoimmune diseases. In this review, we summarize key recent developments and propose a unifying model for the role of IDO in tolerance induction.
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              Compounds with Therapeutic Potential against Novel Respiratory 2019 Coronavirus

              Currently, the expansion of the novel human respiratory coronavirus (known as SARS-CoV-2 [severe acute respiratory syndrome coronavirus 2], COVID-2019 [coronavirus disease 2019], or 2019-nCoV [2019 novel coronavirus]) has stressed the need for therapeutic alternatives to alleviate and stop this new epidemic. The previous epidemics of infections by high-morbidity human coronaviruses, such as SARS-CoV in 2003 and the Middle East respiratory syndrome coronavirus (MERS-CoV) in 2012, prompted the characterization of compounds that could be potentially active against the currently emerging novel coronavirus, SARS-CoV-2.
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                Author and article information

                Journal
                Virus Res
                Virus Res
                Virus Research
                Elsevier B.V.
                0168-1702
                1872-7492
                18 October 2020
                18 October 2020
                : 198202
                Affiliations
                [a ]Center for Natural and Human Sciences (CCNH), Federal University of ABC (UFABC), Santo André, SP, Brazil
                [b ]Department of Chemical Engineering, Universidad de La Frontera, Temuco, Chile
                [c ]Centro de Excelencia en Investigación Biotecnologica Aplicada al Medio Ambiente (CIBAMA-BIOREN), Universidad de La Frontera, Temuco, Chile
                [d ]Centre for Inflammation Research, University of Edinburgh, 47 Little France Crescent, Edinburgh, EH16 4TJ, UK
                Author notes
                [* ]Corresponding author at: Center for Natural and Human Sciences (CCNH), Federal University of ABC (UFABC), Av. dos Estados 5001, CEP 09210-580, Santo André, SP, Brazil.
                Article
                S0168-1702(20)31109-6 198202
                10.1016/j.virusres.2020.198202
                7568847
                33086123
                29ebdd2e-c866-4a79-aa8f-fc32dac42949
                © 2020 Elsevier B.V. All rights reserved.

                Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.

                History
                : 18 July 2020
                : 11 October 2020
                : 14 October 2020
                Categories
                Review

                Microbiology & Virology
                cunps, copper nanoparticles,ido, indoleamine 2,3–dioxygenase,inos, inducible no synthase,no, nitric oxide,nox, nitrogen reactive species,onoo-, peroxynitrite,rna, ribonucleic acid,sars-cov-2, severe acute respiratory syndrome corona virus 2,agnps, silver nanoparticles,snap, s-nitroso-n-acetylpenicillamine,o2•-, superoxide,uva, ultraviolet radiation a,fda, us food and drug administration,who, world health organization,inhaled nitric oxide,covid-19,sars-cov,nanoparticles,antiviral

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