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      Hydroxychloroquine in rheumatic autoimmune disorders and beyond

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          Abstract

          Initially used as antimalarial drugs, hydroxychloroquine ( HCQ) and, to a lesser extent, chloroquine ( CQ) are currently being used to treat several diseases. Due to its cost‐effectiveness, safety and efficacy, HCQ is especially used in rheumatic autoimmune disorders ( RADs), such as systemic lupus erythematosus, primary Sjögren's syndrome and rheumatoid arthritis. Despite this widespread use in the clinic, HCQ molecular modes of action are still not completely understood. By influencing several cellular pathways through different mechanisms, CQ and HCQ inhibit multiple endolysosomal functions, including autophagy, as well as endosomal Toll‐like receptor activation and calcium signalling. These effects alter several aspects of the immune system with the synergistic consequence of reducing pro‐inflammatory cytokine production and release, one of the most marked symptoms of RADs. Here, we review the current knowledge on the molecular modes of action of these drugs and the circumstances under which they trigger side effects. This is of particular importance as the therapeutic use of HCQ is expanding beyond the treatment of malaria and RADs.

          Abstract

          Hydroxychloroquine has been heavily discussed in the context of COVID19, but this anti‐malarial drug is primarily used in rheumatic autoimmune disorders ( RADs). This comprehensive review recapitulates our knowledge on the mode of action of this drug in RADs, and on its potential applications and side effects.

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          In Vitro Antiviral Activity and Projection of Optimized Dosing Design of Hydroxychloroquine for the Treatment of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2)

          Abstract Background The Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) first broke out in Wuhan (China) and subsequently spread worldwide. Chloroquine has been sporadically used in treating SARS-CoV-2 infection. Hydroxychloroquine shares the same mechanism of action as chloroquine, but its more tolerable safety profile makes it the preferred drug to treat malaria and autoimmune conditions. We propose that the immunomodulatory effect of hydroxychloroquine also may be useful in controlling the cytokine storm that occurs late-phase in critically ill SARS-CoV-2 infected patients. Currently, there is no evidence to support the use of hydroxychloroquine in SARS-CoV-2 infection. Methods The pharmacological activity of chloroquine and hydroxychloroquine was tested using SARS-CoV-2 infected Vero cells. Physiologically-based pharmacokinetic models (PBPK) were implemented for both drugs separately by integrating their in vitro data. Using the PBPK models, hydroxychloroquine concentrations in lung fluid were simulated under 5 different dosing regimens to explore the most effective regimen whilst considering the drug’s safety profile. Results Hydroxychloroquine (EC50=0.72 μM) was found to be more potent than chloroquine (EC50=5.47 μM) in vitro. Based on PBPK models results, a loading dose of 400 mg twice daily of hydroxychloroquine sulfate given orally, followed by a maintenance dose of 200 mg given twice daily for 4 days is recommended for SARS-CoV-2 infection, as it reached three times the potency of chloroquine phosphate when given 500 mg twice daily 5 days in advance. Conclusions Hydroxychloroquine was found to be more potent than chloroquine to inhibit SARS-CoV-2 in vitro.
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            Cytokine release syndrome in severe COVID-19

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              A Randomized Trial of Hydroxychloroquine as Postexposure Prophylaxis for Covid-19

              Abstract Background Coronavirus disease 2019 (Covid-19) occurs after exposure to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). For persons who are exposed, the standard of care is observation and quarantine. Whether hydroxychloroquine can prevent symptomatic infection after SARS-CoV-2 exposure is unknown. Methods We conducted a randomized, double-blind, placebo-controlled trial across the United States and parts of Canada testing hydroxychloroquine as postexposure prophylaxis. We enrolled adults who had household or occupational exposure to someone with confirmed Covid-19 at a distance of less than 6 ft for more than 10 minutes while wearing neither a face mask nor an eye shield (high-risk exposure) or while wearing a face mask but no eye shield (moderate-risk exposure). Within 4 days after exposure, we randomly assigned participants to receive either placebo or hydroxychloroquine (800 mg once, followed by 600 mg in 6 to 8 hours, then 600 mg daily for 4 additional days). The primary outcome was the incidence of either laboratory-confirmed Covid-19 or illness compatible with Covid-19 within 14 days. Results We enrolled 821 asymptomatic participants. Overall, 87.6% of the participants (719 of 821) reported a high-risk exposure to a confirmed Covid-19 contact. The incidence of new illness compatible with Covid-19 did not differ significantly between participants receiving hydroxychloroquine (49 of 414 [11.8%]) and those receiving placebo (58 of 407 [14.3%]); the absolute difference was −2.4 percentage points (95% confidence interval, −7.0 to 2.2; P=0.35). Side effects were more common with hydroxychloroquine than with placebo (40.1% vs. 16.8%), but no serious adverse reactions were reported. Conclusions After high-risk or moderate-risk exposure to Covid-19, hydroxychloroquine did not prevent illness compatible with Covid-19 or confirmed infection when used as postexposure prophylaxis within 4 days after exposure. (Funded by David Baszucki and Jan Ellison Baszucki and others; ClinicalTrials.gov number, NCT04308668.)
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                Author and article information

                Contributors
                m.mauthe@umcg.nl
                Journal
                EMBO Mol Med
                EMBO Mol Med
                10.1002/(ISSN)1757-4684
                EMMM
                embomm
                EMBO Molecular Medicine
                John Wiley and Sons Inc. (Hoboken )
                1757-4676
                1757-4684
                26 July 2020
                07 August 2020
                : 12
                : 8 ( doiID: 10.1002/emmm.v12.8 )
                : e12476
                Affiliations
                [ 1 ] Department of Biomedical Sciences of Cells and Systems University of Groningen University Medical Center Groningen Groningen The Netherlands
                Author notes
                [*] [* ]Corresponding author. Tel: +31 6 25646762; E‐mail: m.mauthe@ 123456umcg.nl
                Author information
                https://orcid.org/0000-0003-2652-2686
                https://orcid.org/0000-0003-0049-7961
                Article
                EMMM202012476
                10.15252/emmm.202012476
                7411564
                32715647
                d922cbdf-8514-4bd1-98e9-8708d60925b8
                © 2020 The Authors. Published under the terms of the CC BY 4.0 license

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 08 April 2020
                : 02 July 2020
                : 03 July 2020
                Page count
                Figures: 3, Tables: 0, Pages: 17, Words: 15649
                Funding
                Funded by: ZonMw (Netherlands Organisation for Health Research and Development) , open-funder-registry 10.13039/501100001826;
                Award ID: 91217002
                Funded by: Nederlandse Organisatie voor Wetenschappelijk Onderzoek (NWO) , open-funder-registry 10.13039/501100003246;
                Award ID: ALWOP.310
                Funded by: EC|H2020|H2020 Priority Excellent Science|H2020 Marie Skłodowska-Curie Actions (MSCA) , open-funder-registry 10.13039/100010665;
                Award ID: 713660
                Award ID: 765912
                Categories
                Review
                Reviews
                Custom metadata
                2.0
                07 August 2020
                Converter:WILEY_ML3GV2_TO_JATSPMC version:5.8.6 mode:remove_FC converted:07.08.2020

                Molecular medicine
                calcium,chloroquine,cytokines,lysosome,toll‐like receptors,immunology,chemical biology

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