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      Nrf2-interacting nutrients and COVID-19: time for research to develop adaptation strategies

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          Abstract

          There are large between- and within-country variations in COVID-19 death rates. Some very low death rate settings such as Eastern Asia, Central Europe, the Balkans and Africa have a common feature of eating large quantities of fermented foods whose intake is associated with the activation of the Nrf2 (Nuclear factor (erythroid-derived 2)-like 2) anti-oxidant transcription factor. There are many Nrf2-interacting nutrients (berberine, curcumin, epigallocatechin gallate, genistein, quercetin, resveratrol, sulforaphane) that all act similarly to reduce insulin resistance, endothelial damage, lung injury and cytokine storm. They also act on the same mechanisms (mTOR: Mammalian target of rapamycin, PPARγ:Peroxisome proliferator-activated receptor, NFκB: Nuclear factor kappa B, ERK: Extracellular signal-regulated kinases and eIF2α:Elongation initiation factor 2α). They may as a result be important in mitigating the severity of COVID-19, acting through the endoplasmic reticulum stress or ACE-Angiotensin-II-AT 1R axis (AT 1R) pathway. Many Nrf2-interacting nutrients are also interacting with TRPA1 and/or TRPV1. Interestingly, geographical areas with very low COVID-19 mortality are those with the lowest prevalence of obesity (Sub-Saharan Africa and Asia). It is tempting to propose that Nrf2-interacting foods and nutrients can re-balance insulin resistance and have a significant effect on COVID-19 severity. It is therefore possible that the intake of these foods may restore an optimal natural balance for the Nrf2 pathway and may be of interest in the mitigation of COVID-19 severity.

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          Projecting the transmission dynamics of SARS-CoV-2 through the postpandemic period

          It is urgent to understand the future of severe acute respiratory syndrome–coronavirus 2 (SARS-CoV-2) transmission. We used estimates of seasonality, immunity, and cross-immunity for betacoronaviruses OC43 and HKU1 from time series data from the USA to inform a model of SARS-CoV-2 transmission. We projected that recurrent wintertime outbreaks of SARS-CoV-2 will probably occur after the initial, most severe pandemic wave. Absent other interventions, a key metric for the success of social distancing is whether critical care capacities are exceeded. To avoid this, prolonged or intermittent social distancing may be necessary into 2022. Additional interventions, including expanded critical care capacity and an effective therapeutic, would improve the success of intermittent distancing and hasten the acquisition of herd immunity. Longitudinal serological studies are urgently needed to determine the extent and duration of immunity to SARS-CoV-2. Even in the event of apparent elimination, SARS-CoV-2 surveillance should be maintained since a resurgence in contagion could be possible as late as 2024.
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            Transcriptional Regulation by Nrf2

            Abstract Significance: Nuclear factor E2-related factor 2 (Nrf2) is a transcription factor that coordinates the basal and stress-inducible activation of a vast array of cytoprotective genes. Understanding the regulation of Nrf2 activity and downstream pathways has major implications for human health. Recent Advances: Nrf2 regulates the transcription of components of the glutathione and thioredoxin antioxidant systems, as well as enzymes involved in phase I and phase II detoxification of exogenous and endogenous products, NADPH regeneration, and heme metabolism. It therefore represents a crucial regulator of the cellular defense mechanisms against xenobiotic and oxidative stress. In addition to antioxidant responses, Nrf2 is involved in other cellular processes, such as autophagy, intermediary metabolism, stem cell quiescence, and unfolded protein response. Given the wide range of processes that Nrf2 controls, its activity is tightly regulated at multiple levels. Here, we review the different modes of regulation of Nrf2 activity and the current knowledge of Nrf2-mediated transcriptional control. Critical Issues: It is now clear that Nrf2 lies at the center of a complex regulatory network. A full comprehension of the Nrf2 program will require an integrated consideration of all the different factors determining Nrf2 activity. Future Directions: Additional computational and experimental studies are needed to obtain a more dynamic global view of Nrf2-mediated gene regulation. In particular, studies comparing how the Nrf2-dependent network changes from a physiological to a pathological condition can provide insight into mechanisms of disease and instruct new treatment strategies.
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              Itaconate is an anti-inflammatory metabolite that activates Nrf2 via alkylation of KEAP1

              The endogenous metabolite itaconate has recently emerged as a regulator of macrophage function, but its precise mechanism of action remains poorly understood. Here we show that itaconate is required for the activation of the anti-inflammatory transcription factor Nrf2 (also known as NFE2L2) by lipopolysaccharide in mouse and human macrophages. We find that itaconate directly modifies proteins via alkylation of cysteine residues. Itaconate alkylates cysteine residues 151, 257, 288, 273 and 297 on the protein KEAP1, enabling Nrf2 to increase the expression of downstream genes with anti-oxidant and anti-inflammatory capacities. The activation of Nrf2 is required for the anti-inflammatory action of itaconate. We describe the use of a new cell-permeable itaconate derivative, 4-octyl itaconate, which is protective against lipopolysaccharide-induced lethality in vivo and decreases cytokine production. We show that type I interferons boost the expression of Irg1 (also known as Acod1) and itaconate production. Furthermore, we find that itaconate production limits the type I interferon response, indicating a negative feedback loop that involves interferons and itaconate. Our findings demonstrate that itaconate is a crucial anti-inflammatory metabolite that acts via Nrf2 to limit inflammation and modulate type I interferons.
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                Author and article information

                Contributors
                jean.bousquet@orange.fr
                Journal
                Clin Transl Allergy
                Clin Transl Allergy
                Clinical and Translational Allergy
                BioMed Central (London )
                2045-7022
                3 December 2020
                3 December 2020
                2020
                : 10
                : 58
                Affiliations
                [1 ]Department of Dermatology and Allergy, Charité, Universitätsmedizin Berlin, Humboldt-Universität Zu Berlin, Berlin Institute of Health, Comprehensive Allergy Center, Berlin, Germany
                [2 ]GRID grid.157868.5, ISNI 0000 0000 9961 060X, University Hospital Montpellier, ; 273 avenue d’Occitanie, 34090 Montpellier, France
                [3 ]MACVIA-France, Montpellier, France
                [4 ]Laboratoire de Biochimie et Hormonologie, PhyMedExp, Université de Montpellier, INSERM, CNRS, CHU, Montpellier, France
                [5 ]Medical Consulting Czarlewski, Levallois, France
                [6 ]MASK-Air, Montpellier, France
                [7 ]GRID grid.411142.3, ISNI 0000 0004 1767 8811, IMIM (Hospital del Mar Research Institute), ; Barcelona, Spain
                [8 ]GRID grid.5612.0, ISNI 0000 0001 2172 2676, Universitat Pompeu Fabra (UPF), ; Barcelona, Spain
                [9 ]GRID grid.413448.e, ISNI 0000 0000 9314 1427, CIBER Epidemiología y Salud Pública (CIBERESP), ; Barcelona, Spain
                [10 ]GRID grid.434607.2, ISNI 0000 0004 1763 3517, ISGlobAL, Barcelona, Centre for Research in Environmental Epidemiology (CREAL), ; Barcelona, Spain
                [11 ]GRID grid.4868.2, ISNI 0000 0001 2171 1133, Institute for Population Health Sciences, Barts and The London School of Medicine and Dentistry, , Queen Mary University of London, ; London, UK
                [12 ]Skin and Allergy Hospital, Helsinki University Hospital, and University of Helsinki, Helsinki, Finland
                [13 ]GRID grid.5808.5, ISNI 0000 0001 1503 7226, GreenUPorto - Sustainable Agrifood Production Research Centre, DGAOT, Faculty of Sciences, , University of Porto, ; Campus de Vairão, Vila do Conde, Portugal
                [14 ]GRID grid.4691.a, ISNI 0000 0001 0790 385X, Department of Advanced Biomedical Sciences, , Federico II University, ; Napoli, Italy
                [15 ]GRID grid.157868.5, ISNI 0000 0000 9961 060X, Department of Geriatrics, , Montpellier University Hospital, ; Montpellier, France
                [16 ]GRID grid.414125.7, ISNI 0000 0001 0727 6809, Division of Allergy, Department of Pediatric Medicine, , The Bambino Gesu Children’s Research Hospital Holy See, ; Rome, Italy
                [17 ]GRID grid.414603.4, Personalized Medicine Asthma and Allergy Clinic-Humanitas University & Research Hospital, IRCCS, ; Milano, Italy
                [18 ]GRID grid.5808.5, ISNI 0000 0001 1503 7226, CINTESIS, Center for Research in Health Technology and Information Systems, , Faculdade de Medicina da Universidade do Porto; and Medida,, ; Lda Porto, Porto, Portugal
                [19 ]World Business Council for Sustainable Development (WBCSD) Maison de la Paix, Geneva, Switzerland
                [20 ]GRID grid.417885.7, ISNI 0000 0001 2185 8223, AgroParisTech-Paris Institute of Technology for Life, Food and Environmental Sciences, ; Paris, France
                [21 ]Microbiology and Functionality Research Group, Research and Development Division, World Institute of Kimchi, Gwangju, Korea
                [22 ]SME Service Department, Strategy and Planning Division, World Institute of Kimchi, Gwangju, Korea
                [23 ]GRID grid.157868.5, ISNI 0000 0000 9961 060X, Maladies Infectieuses et Tropicales, CHU, ; Montpellier, France
                [24 ]GRID grid.4305.2, ISNI 0000 0004 1936 7988, The Usher Institute of Population Health Sciences and Informatics, , The University of Edinburgh, ; Edinburgh, UK
                [25 ]GRID grid.7400.3, ISNI 0000 0004 1937 0650, Swiss Institute of Allergy and Asthma Research (SIAF), , University of Zurich, ; Davos, Switzerland
                Author information
                http://orcid.org/0000-0001-9226-7762
                Article
                362
                10.1186/s13601-020-00362-7
                7711617
                33292691
                5ddc894c-9cac-41ce-b0da-91cc386467d5
                © The Author(s) 2020

                Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

                History
                : 30 September 2020
                : 12 November 2020
                Funding
                Funded by: MASK-Air
                Funded by: Aria
                Categories
                Review
                Custom metadata
                © The Author(s) 2020

                Immunology
                covid-19,nrf2,foods,nutrients,insulin resistance,obesity,trpa1
                Immunology
                covid-19, nrf2, foods, nutrients, insulin resistance, obesity, trpa1

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