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      The effect of allergy and asthma as a comorbidity on the susceptibility and outcomes of COVID-19

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          Abstract

          The coronavirus disease 2019 (COVID-19) pandemic causes an overwhelming number of hospitalization and deaths with a significant socioeconomic impact. The vast majority of studies indicate that asthma and allergic diseases do not represent a risk factor for COVID-19 susceptibility nor cause a more severe course of disease. This raises the opportunity to investigate the underlying mechanisms of the interaction between an allergic background and severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection. The majority of patients with asthma, atopic dermatitis, allergic rhinitis, chronic rhinosinusitis, food allergies and drug allergies exhibit an over-expression of type 2 immune and inflammatory pathways with the contribution of epithelial cells, innate lymphoid cells, dendritic cells, T cells, eosinophils, mast cells, basophils, and the type 2 cytokines interleukin (IL)-4, IL-5, IL-9, IL-13, and IL-31. The potential impact of type 2 inflammation-related allergic diseases on susceptibility to COVID-19 and severity of its course have been reported. In this review, the prevalence of asthma and other common allergic diseases in COVID-19 patients is addressed. Moreover, the impact of allergic and non-allergic asthma with different severity and control status, currently available asthma treatments such as inhaled and oral corticosteroids, short- and long-acting β2 agonists, leukotriene receptor antagonists and biologicals on the outcome of COVID-19 patients is reviewed. In addition, possible protective mechanisms of asthma and type 2 inflammation on COVID-19 infection, such as the expression of SARS-CoV-2 entry receptors, antiviral activity of eosinophils and cross-reactive T-cell epitopes, are discussed. Potential interactions of other allergic diseases with COVID-19 are postulated, including recommendations for their management.

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          OpenSAFELY: factors associated with COVID-19 death in 17 million patients

          COVID-19 has rapidly impacted on mortality worldwide. 1 There is unprecedented urgency to understand who is most at risk of severe outcomes, requiring new approaches for timely analysis of large datasets. Working on behalf of NHS England we created OpenSAFELY: a secure health analytics platform covering 40% of all patients in England, holding patient data within the existing data centre of a major primary care electronic health records vendor. Primary care records of 17,278,392 adults were pseudonymously linked to 10,926 COVID-19 related deaths. COVID-19 related death was associated with: being male (hazard ratio 1.59, 95%CI 1.53-1.65); older age and deprivation (both with a strong gradient); diabetes; severe asthma; and various other medical conditions. Compared to people with white ethnicity, black and South Asian people were at higher risk even after adjustment for other factors (HR 1.48, 1.29-1.69 and 1.45, 1.32-1.58 respectively). We have quantified a range of clinical risk factors for COVID-19 related death in the largest cohort study conducted by any country to date. OpenSAFELY is rapidly adding further patients’ records; we will update and extend results regularly.
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            Cell entry mechanisms of SARS-CoV-2

            Significance A key to curbing SARS-CoV-2 is to understand how it enters cells. SARS-CoV-2 and SARS-CoV both use human ACE2 as entry receptor and human proteases as entry activators. Using biochemical and pseudovirus entry assays and SARS-CoV as a comparison, we have identified key cell entry mechanisms of SARS-CoV-2 that potentially contribute to the immune evasion, cell infectivity, and wide spread of the virus. This study also clarifies conflicting reports from recent studies on cell entry of SARS-CoV-2. Finally, by highlighting the potency and the evasiveness of SARS-CoV-2, the study provides insight into intervention strategies that target its cell entry mechanisms.
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              Clinical characteristics of 140 patients infected by SARS‐CoV‐2 in Wuhan, China

              Coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection has been widely spread. We aim to investigate the clinical characteristic and allergy status of patients infected with SARS-CoV-2.
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                Author and article information

                Journal
                Int Immunol
                Int Immunol
                intimm
                International Immunology
                Oxford University Press (UK )
                0953-8178
                1460-2377
                12 November 2021
                12 November 2021
                : dxab107
                Affiliations
                [1 ] Department of Allergology, Zhongnan Hospital of Wuhan University , Wuhan, Hubei, China
                [2 ] Hubei Province Key Laboratory of Allergy and Immunology, Wuhan University , Wuhan, Hubei, China
                [3 ] Faculty of Medicine, Transylvania University , Brasov, Romania
                [4 ] Swiss Institute of Allergy and Asthma Research (SIAF), University of Zurich , Herman-Burchard Strasse, Davos, Switzerland
                [5 ] Sean N. Parker Center for Allergy and Asthma Research, Department of Medicine, Stanford University , Palo Alto, CA, USA
                [6 ] Center for Rhinology and Allergology , An den Quellen, Wiesbaden, Germany
                [7 ] Department of Clinical Immunology, Wrocław Medical University , Wrocław, Poland
                [8 ] All-MED Medical Research Institute , Wrocław, Poland
                Author notes
                Correspondence to: C. A. Akdis; E-mail: akdisac@ 123456siaf.uzh.ch
                Author information
                https://orcid.org/0000-0003-1251-7608
                Article
                dxab107
                10.1093/intimm/dxab107
                8689956
                34788827
                3f98f0bf-c1e5-42e9-aad2-779dd28d6ab5
                © The Japanese Society for Immunology. 2021. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com

                This article is published and distributed under the terms of the Oxford University Press, Standard Journals Publication Model ( https://academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model)

                This article is made available via the PMC Open Access Subset for unrestricted re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the COVID-19 pandemic or until permissions are revoked in writing. Upon expiration of these permissions, PMC is granted a perpetual license to make this article available via PMC and Europe PMC, consistent with existing copyright protections.

                History
                : 04 October 2021
                : 09 November 2021
                : 10 November 2021
                : 11 December 2021
                Page count
                Pages: 12
                Categories
                Invited Review
                AcademicSubjects/MED00730
                Custom metadata
                PAP
                corrected-proof

                Immunology
                angiotensin-converting enzyme 2,mortality,sars-cov-2,susceptibility,severity
                Immunology
                angiotensin-converting enzyme 2, mortality, sars-cov-2, susceptibility, severity

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