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      Acute severe hepatitis outbreak in children: A perfect storm. What do we know, and what questions remain?

      review-article
      1 , 2 , 3 , 4 , 5 , 6 , 7 , 8 , 9 , 10 , 11 , 12 , 13 , 14 , 15 , 16 , 17 , 18 , 19 , 20 , 21 , 22 , 23 , 24 , 25 , 26 , 27 , 28 , * , , and ESCMID Study Group for Viral Hepatitis (ESGVH)
      Frontiers in Pharmacology
      Frontiers Media S.A.
      paediatric, hepatitis, outbreak, adenovirus, adeno-associated virus, epidemiology, aetiology, liver

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          Abstract

          During the first half of 2022, the World Health Organization reported an outbreak of acute severe hepatitis of unknown aetiology (AS-Hep-UA) in children, following initial alerts from the United Kingdom (UK) where a cluster of cases was first observed in previously well children aged <6 years. Sporadic cases were then reported across Europe and worldwide, although in most countries incidence did not increase above the expected baseline. There were no consistent epidemiological links between cases, and microbiological investigations ruled out known infectious causes of hepatitis. In this review, we explore the evidence for the role of viral infection, superimposed on a specific host genetic background, as a trigger for liver pathology. This hypothesis is based on a high prevalence of Human Adenovirus (HAdV) 41F in affected children, together with metagenomic evidence of adeno-associated virus (Adeno-associated viruses)-2, which is a putative trigger for an immune-mediated liver injury. Roles for superantigen-mediated pathology have also been explored, with a focus on the potential contribution of SARS-CoV-2 infection. Affected children also had a high frequency of the MHC allele HLA-DRB1*04:01, supporting an immunological predisposition, and may have been vulnerable to viral coinfections due to disruption in normal patterns of exposure and immunity as a result of population lockdowns during the COVID-19 pandemic. We discuss areas of ongoing uncertainty, and highlight the need for ongoing scrutiny to inform clinical and public health interventions for this outbreak and for others that may evolve in future.

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          Most cited references104

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          Clinical course and risk factors for mortality of adult inpatients with COVID-19 in Wuhan, China: a retrospective cohort study

          Summary Background Since December, 2019, Wuhan, China, has experienced an outbreak of coronavirus disease 2019 (COVID-19), caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Epidemiological and clinical characteristics of patients with COVID-19 have been reported but risk factors for mortality and a detailed clinical course of illness, including viral shedding, have not been well described. Methods In this retrospective, multicentre cohort study, we included all adult inpatients (≥18 years old) with laboratory-confirmed COVID-19 from Jinyintan Hospital and Wuhan Pulmonary Hospital (Wuhan, China) who had been discharged or had died by Jan 31, 2020. Demographic, clinical, treatment, and laboratory data, including serial samples for viral RNA detection, were extracted from electronic medical records and compared between survivors and non-survivors. We used univariable and multivariable logistic regression methods to explore the risk factors associated with in-hospital death. Findings 191 patients (135 from Jinyintan Hospital and 56 from Wuhan Pulmonary Hospital) were included in this study, of whom 137 were discharged and 54 died in hospital. 91 (48%) patients had a comorbidity, with hypertension being the most common (58 [30%] patients), followed by diabetes (36 [19%] patients) and coronary heart disease (15 [8%] patients). Multivariable regression showed increasing odds of in-hospital death associated with older age (odds ratio 1·10, 95% CI 1·03–1·17, per year increase; p=0·0043), higher Sequential Organ Failure Assessment (SOFA) score (5·65, 2·61–12·23; p<0·0001), and d-dimer greater than 1 μg/mL (18·42, 2·64–128·55; p=0·0033) on admission. Median duration of viral shedding was 20·0 days (IQR 17·0–24·0) in survivors, but SARS-CoV-2 was detectable until death in non-survivors. The longest observed duration of viral shedding in survivors was 37 days. Interpretation The potential risk factors of older age, high SOFA score, and d-dimer greater than 1 μg/mL could help clinicians to identify patients with poor prognosis at an early stage. Prolonged viral shedding provides the rationale for a strategy of isolation of infected patients and optimal antiviral interventions in the future. Funding Chinese Academy of Medical Sciences Innovation Fund for Medical Sciences; National Science Grant for Distinguished Young Scholars; National Key Research and Development Program of China; The Beijing Science and Technology Project; and Major Projects of National Science and Technology on New Drug Creation and Development.
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            SARS-CoV-2 Cell Entry Depends on ACE2 and TMPRSS2 and Is Blocked by a Clinically Proven Protease Inhibitor

            Summary The recent emergence of the novel, pathogenic SARS-coronavirus 2 (SARS-CoV-2) in China and its rapid national and international spread pose a global health emergency. Cell entry of coronaviruses depends on binding of the viral spike (S) proteins to cellular receptors and on S protein priming by host cell proteases. Unravelling which cellular factors are used by SARS-CoV-2 for entry might provide insights into viral transmission and reveal therapeutic targets. Here, we demonstrate that SARS-CoV-2 uses the SARS-CoV receptor ACE2 for entry and the serine protease TMPRSS2 for S protein priming. A TMPRSS2 inhibitor approved for clinical use blocked entry and might constitute a treatment option. Finally, we show that the sera from convalescent SARS patients cross-neutralized SARS-2-S-driven entry. Our results reveal important commonalities between SARS-CoV-2 and SARS-CoV infection and identify a potential target for antiviral intervention.
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              Epidemiological and clinical characteristics of 99 cases of 2019 novel coronavirus pneumonia in Wuhan, China: a descriptive study

              Summary Background In December, 2019, a pneumonia associated with the 2019 novel coronavirus (2019-nCoV) emerged in Wuhan, China. We aimed to further clarify the epidemiological and clinical characteristics of 2019-nCoV pneumonia. Methods In this retrospective, single-centre study, we included all confirmed cases of 2019-nCoV in Wuhan Jinyintan Hospital from Jan 1 to Jan 20, 2020. Cases were confirmed by real-time RT-PCR and were analysed for epidemiological, demographic, clinical, and radiological features and laboratory data. Outcomes were followed up until Jan 25, 2020. Findings Of the 99 patients with 2019-nCoV pneumonia, 49 (49%) had a history of exposure to the Huanan seafood market. The average age of the patients was 55·5 years (SD 13·1), including 67 men and 32 women. 2019-nCoV was detected in all patients by real-time RT-PCR. 50 (51%) patients had chronic diseases. Patients had clinical manifestations of fever (82 [83%] patients), cough (81 [82%] patients), shortness of breath (31 [31%] patients), muscle ache (11 [11%] patients), confusion (nine [9%] patients), headache (eight [8%] patients), sore throat (five [5%] patients), rhinorrhoea (four [4%] patients), chest pain (two [2%] patients), diarrhoea (two [2%] patients), and nausea and vomiting (one [1%] patient). According to imaging examination, 74 (75%) patients showed bilateral pneumonia, 14 (14%) patients showed multiple mottling and ground-glass opacity, and one (1%) patient had pneumothorax. 17 (17%) patients developed acute respiratory distress syndrome and, among them, 11 (11%) patients worsened in a short period of time and died of multiple organ failure. Interpretation The 2019-nCoV infection was of clustering onset, is more likely to affect older males with comorbidities, and can result in severe and even fatal respiratory diseases such as acute respiratory distress syndrome. In general, characteristics of patients who died were in line with the MuLBSTA score, an early warning model for predicting mortality in viral pneumonia. Further investigation is needed to explore the applicability of the MuLBSTA score in predicting the risk of mortality in 2019-nCoV infection. Funding National Key R&D Program of China.
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                Author and article information

                Contributors
                Journal
                Front Pharmacol
                Front Pharmacol
                Front. Pharmacol.
                Frontiers in Pharmacology
                Frontiers Media S.A.
                1663-9812
                25 November 2022
                2022
                : 13
                : 1062408
                Affiliations
                [1] 1 The Francis Crick Institute , London, United Kingdom
                [2] 2 Division of Infection and Immunity , University College London , London, United Kingdom
                [3] 3 Department of Infection , University College London Hospitals , London, United Kingdom
                [4] 4 Nuffield Department of Medicine , University of Oxford , Oxford, England
                [5] 5 Department of Infectious Diseases , National Institute for Infectious Diseases-Prof. Dr. Matei Balş , Carol Davila University of Medicine and Pharmacy , Bucharest, Romania
                [6] 6 Faculty of Medicine , Clinic for Infectious Diseases and Febrile Illnesses , University Medical Centre Ljubljana , University of Ljubljana , Ljubljana, Slovenia
                [7] 7 Virology Department , Stefan S. Nicolau Institute of Virology , “Carol Davila” University of Medicine and Pharmacy , Bucharest, Romania
                [8] 8 Hospital Universitario Reina Sofía , Instituto Maimónides de Investigación Biomédica de Córdoba , Universidad de Córdoba , Córdoba, Spain
                [9] 9 Department of Internal Medicine and Infectious Diseases , University Medical Centre Utrecht , Utrecht, Netherlands
                [10] 10 INSERM U1052 , Department of Intensive Care Unit , Hôpital Lyon Sud , Hospices Civils de Lyon , Université Claude Bernard Lyon 1 , Lyon, France
                [11] 11 Microbiology Department , Instituto de Investigacion Ibs.Granada and Ciber de Enfermedades Infecciosas (CIBERINFEC) , University Hospital San Cecilio , Granada, Spain
                [12] 12 Department of Infectious Diseases , “Dr. Victor Babes” Clinical Hospital of Infectious and Tropical Diseases , Bucharest, Romania
                [13] 13 Department of Infectious Diseases and Clinical Microbiology , Ankara University Faculty of Medicine , Ankara, Turkey
                [14] 14 Department of Infectious Disease and Clinical Microbiology , Ankara City Hospital , Ankara Yıldırım Beyazıt University , Ankara, Turkey
                [15] 15 Clinic for Infectious and Tropical Diseases , University Clinical Center of Serbia , Belgrade, Serbia
                [16] 16 Division of Infectious Diseases , Ospedale Policlinico San Martino , Genova, Italy
                [17] 17 Nephrology and Infectious Diseases R&D , Infectious Diseases Intensive Care Unit , Faculty of Medicine of University of Porto , Centro Hospitalar Universitário São João , I3S - Instituto de Investigação e Inovaçãoem Saúde , University of Porto , Porto, Portugal
                [18] 18 Ministry of Health , National Centre for Infectious Diseases , National Institute of Health , Yerevan, Armenia
                [19] 19 Infectious Diseases Hospital Prof. Ivan Kirov and Department of Infectious Diseases , Parasitology and Tropical Medicine , Medical University of Sofia , Sofia, Bulgaria
                [20] 20 Department of Microbiology , Public Health Institute Novi Pazar , Novi Pazar, Serbia
                [21] 21 Department of Virology , INSERM , Henri Mondor Hospital , Assistance Publique-Hôpitaux de Paris , Institut Mondor de Recherche Biomédicale , Université Paris-Est , Créteil, France
                [22] 22 Department of Immunological and Molecular Diagnostics , University Hospital for Infectious Diseases “Dr Fran Mihaljevic” , Zagreb, Croatia
                [23] 23 Medical Research Council-University of Glasgow Centre for Virus Research , University of Glasgow , Glasgow, United Kingdom
                [24] 24 Department of Microbiology , Oslo University Hospital , Institute of Clinical Medicine , University of Oslo , Oslo, Norway
                [25] 25 National Institute for Mother and Child Health “Alessandrescu-Rusescu” , Carol Davila University of Medicine and Pharmacy , Bucharest, Romania
                [26] 26 NIHR Biomedical Research Centre , Nottingham University Hospitals NHS Trust and the University of Nottingham , Nottingham, United Kingdom
                [27] 27 Department of Laboratory Medicine , Section of Clinical Microbiology , Region Skåne , Lund, Sweden
                [28] 28 Department of Translational Medicine , Lund University , Malmö, Sweden
                Author notes

                Edited by: Talha Bin Emran, Begum Gulchemonara Trust University, Bangladesh

                Reviewed by: Mohsina Patwekar, Mohsina Patwekar, India

                Mohammed Mahbubul Matin, University of Chittagong, Bangladesh

                *Correspondence: Gülşen Özkaya Şahin, gulsen.ozkaya_sahin@ 123456med.lu.se
                [ † ]

                These authors have contributed equally to this work and share first authorship

                [ ‡ ]

                These authors have contributed equally to this work and share last authorship

                This article was submitted to Gastrointestinal and Hepatic Pharmacology, a section of the journal Frontiers in Pharmacology

                Article
                1062408
                10.3389/fphar.2022.1062408
                9732095
                36506522
                5c6bf3f7-61bb-498e-b445-dc1e2072ee77
                Copyright © 2022 Matthews, Campbell, Săndulescu, Matičič, Ruta, Rivero-Juárez, van Welzen, Tan, Garcia, Gherlan, Çınar, Hasanoğlu, Gmizić, Nicolini, Santos, Sargsyants, Velikov, Habibović, Fourati, Židovec-Lepej, Herder, Dudman, Miron, Irving and Şahin.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 05 October 2022
                : 04 November 2022
                Categories
                Pharmacology
                Review

                Pharmacology & Pharmaceutical medicine
                paediatric,hepatitis,outbreak,adenovirus,adeno-associated virus,epidemiology,aetiology,liver

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