Cyclosporine and COVID-19: Risk or favorable?

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

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Cyclosporine and COVID-19 : Risk or favorable? / Poulsen, Nadia Nicholine; von Brunn, Albrecht; Hornum, Mads; Blomberg Jensen, Martin.

I: American Journal of Transplantation, Bind 20, Nr. 11, 2020, s. 2975-2982.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Poulsen, NN, von Brunn, A, Hornum, M & Blomberg Jensen, M 2020, 'Cyclosporine and COVID-19: Risk or favorable?', American Journal of Transplantation, bind 20, nr. 11, s. 2975-2982. https://doi.org/10.1111/ajt.16250

APA

Poulsen, N. N., von Brunn, A., Hornum, M., & Blomberg Jensen, M. (2020). Cyclosporine and COVID-19: Risk or favorable? American Journal of Transplantation, 20(11), 2975-2982. https://doi.org/10.1111/ajt.16250

Vancouver

Poulsen NN, von Brunn A, Hornum M, Blomberg Jensen M. Cyclosporine and COVID-19: Risk or favorable? American Journal of Transplantation. 2020;20(11):2975-2982. https://doi.org/10.1111/ajt.16250

Author

Poulsen, Nadia Nicholine ; von Brunn, Albrecht ; Hornum, Mads ; Blomberg Jensen, Martin. / Cyclosporine and COVID-19 : Risk or favorable?. I: American Journal of Transplantation. 2020 ; Bind 20, Nr. 11. s. 2975-2982.

Bibtex

@article{47bb9680fd92470ab1fe2ddab8781747,
title = "Cyclosporine and COVID-19: Risk or favorable?",
abstract = "The coronavirus disease 2019 (COVID-19) pandemic is declared a global health emergency. COVID-19 is triggered by a novel coronavirus: severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Baseline characteristics of admitted patients with COVID-19 show that adiposity, diabetes, and hypertension are risk factors for developing severe disease, but so far immunosuppressed patients who are listed as high-risk patients have not been more susceptible to severe COVID-19 than the rest of the population. Multiple clinical trials are currently being conducted, which may identify more drugs that can lower mortality, morbidity, and burden on the society. Several independent studies have convincingly shown that cyclosporine inhibit replication of several different coronaviruses in vitro. The cyclosporine-analog alisporivir has recently been shown to inhibit SARS-CoV-2 in vitro. These findings are intriguing, although there is no clinical evidence for a protective effect to reduce the likelihood of severe COVID-19 or to treat the immune storm or acute respiratory distress syndrome (ARDS) that often causes severe morbidity. Here, we review the putative link between COVID-19 and cyclosporine, while we await more robust clinical data.",
keywords = "clinical research/practice, immunosuppressant - calcineurin inhibitor (CNI), immunosuppression/immune modulation, infection and infectious agents - viral, infectious disease, organ transplantation in general",
author = "Poulsen, {Nadia Nicholine} and {von Brunn}, Albrecht and Mads Hornum and {Blomberg Jensen}, Martin",
year = "2020",
doi = "10.1111/ajt.16250",
language = "English",
volume = "20",
pages = "2975--2982",
journal = "American Journal of Transplantation",
issn = "1600-6135",
publisher = "Wiley-Blackwell",
number = "11",

}

RIS

TY - JOUR

T1 - Cyclosporine and COVID-19

T2 - Risk or favorable?

AU - Poulsen, Nadia Nicholine

AU - von Brunn, Albrecht

AU - Hornum, Mads

AU - Blomberg Jensen, Martin

PY - 2020

Y1 - 2020

N2 - The coronavirus disease 2019 (COVID-19) pandemic is declared a global health emergency. COVID-19 is triggered by a novel coronavirus: severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Baseline characteristics of admitted patients with COVID-19 show that adiposity, diabetes, and hypertension are risk factors for developing severe disease, but so far immunosuppressed patients who are listed as high-risk patients have not been more susceptible to severe COVID-19 than the rest of the population. Multiple clinical trials are currently being conducted, which may identify more drugs that can lower mortality, morbidity, and burden on the society. Several independent studies have convincingly shown that cyclosporine inhibit replication of several different coronaviruses in vitro. The cyclosporine-analog alisporivir has recently been shown to inhibit SARS-CoV-2 in vitro. These findings are intriguing, although there is no clinical evidence for a protective effect to reduce the likelihood of severe COVID-19 or to treat the immune storm or acute respiratory distress syndrome (ARDS) that often causes severe morbidity. Here, we review the putative link between COVID-19 and cyclosporine, while we await more robust clinical data.

AB - The coronavirus disease 2019 (COVID-19) pandemic is declared a global health emergency. COVID-19 is triggered by a novel coronavirus: severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Baseline characteristics of admitted patients with COVID-19 show that adiposity, diabetes, and hypertension are risk factors for developing severe disease, but so far immunosuppressed patients who are listed as high-risk patients have not been more susceptible to severe COVID-19 than the rest of the population. Multiple clinical trials are currently being conducted, which may identify more drugs that can lower mortality, morbidity, and burden on the society. Several independent studies have convincingly shown that cyclosporine inhibit replication of several different coronaviruses in vitro. The cyclosporine-analog alisporivir has recently been shown to inhibit SARS-CoV-2 in vitro. These findings are intriguing, although there is no clinical evidence for a protective effect to reduce the likelihood of severe COVID-19 or to treat the immune storm or acute respiratory distress syndrome (ARDS) that often causes severe morbidity. Here, we review the putative link between COVID-19 and cyclosporine, while we await more robust clinical data.

KW - clinical research/practice

KW - immunosuppressant - calcineurin inhibitor (CNI)

KW - immunosuppression/immune modulation

KW - infection and infectious agents - viral

KW - infectious disease

KW - organ transplantation in general

U2 - 10.1111/ajt.16250

DO - 10.1111/ajt.16250

M3 - Journal article

C2 - 32777170

AN - SCOPUS:85090310757

VL - 20

SP - 2975

EP - 2982

JO - American Journal of Transplantation

JF - American Journal of Transplantation

SN - 1600-6135

IS - 11

ER -

ID: 251412237