Anakinra as a potential treatment for COVID-19
Copyright 2023 Clarivate..
On November 8, 2022, the United States Food and Drug Administration (FDA) issued an emergency use authorization for the interleukin-1 (IL-1) inhibitor anakinra for the treatment of patients with COVID-19 pneumonia. The authorization was specifically intended for patients requiring supplemental oxygen who are at risk of progression to respiratory failure and are likely to have an elevated plasma soluble urokinase plasminogen activator receptor. Anakinra is a modified, recombinant human IL-1 receptor antagonist used to treat rheumatoid arthritis, neonatal-onset multisystem inflammatory disease and other inflammatory diseases. This manuscript examines what is known about the role of IL-1 receptor antagonism in the treatment of patients with COVID-19 and examines how anakinra may be used in the future to address the SARS-CoV-2 infection pandemic.
Medienart: |
E-Artikel |
---|
Erscheinungsjahr: |
2023 |
---|---|
Erschienen: |
2023 |
Enthalten in: |
Zur Gesamtaufnahme - volume:59 |
---|---|
Enthalten in: |
Drugs of today (Barcelona, Spain : 1998) - 59(2023), 3 vom: 05. März, Seite 107-112 |
Sprache: |
Englisch |
---|
Beteiligte Personen: |
McCarthy, Matthew W [VerfasserIn] |
---|
Links: |
---|
Themen: |
Anakinra |
---|
Anmerkungen: |
Date Completed 02.03.2023 Date Revised 02.03.2023 published: Print Citation Status MEDLINE |
---|
doi: |
10.1358/dot.2023.59.3.3542446 |
---|
funding: |
|
---|---|
Förderinstitution / Projekttitel: |
|
PPN (Katalog-ID): |
NLM353537373 |
---|
LEADER | 01000naa a22002652 4500 | ||
---|---|---|---|
001 | NLM353537373 | ||
003 | DE-627 | ||
005 | 20231226060229.0 | ||
007 | cr uuu---uuuuu | ||
008 | 231226s2023 xx |||||o 00| ||eng c | ||
024 | 7 | |a 10.1358/dot.2023.59.3.3542446 |2 doi | |
028 | 5 | 2 | |a pubmed24n1178.xml |
035 | |a (DE-627)NLM353537373 | ||
035 | |a (NLM)36847621 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
100 | 1 | |a McCarthy, Matthew W |e verfasserin |4 aut | |
245 | 1 | 0 | |a Anakinra as a potential treatment for COVID-19 |
264 | 1 | |c 2023 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a ƒaComputermedien |b c |2 rdamedia | ||
338 | |a ƒa Online-Ressource |b cr |2 rdacarrier | ||
500 | |a Date Completed 02.03.2023 | ||
500 | |a Date Revised 02.03.2023 | ||
500 | |a published: Print | ||
500 | |a Citation Status MEDLINE | ||
520 | |a Copyright 2023 Clarivate. | ||
520 | |a On November 8, 2022, the United States Food and Drug Administration (FDA) issued an emergency use authorization for the interleukin-1 (IL-1) inhibitor anakinra for the treatment of patients with COVID-19 pneumonia. The authorization was specifically intended for patients requiring supplemental oxygen who are at risk of progression to respiratory failure and are likely to have an elevated plasma soluble urokinase plasminogen activator receptor. Anakinra is a modified, recombinant human IL-1 receptor antagonist used to treat rheumatoid arthritis, neonatal-onset multisystem inflammatory disease and other inflammatory diseases. This manuscript examines what is known about the role of IL-1 receptor antagonism in the treatment of patients with COVID-19 and examines how anakinra may be used in the future to address the SARS-CoV-2 infection pandemic | ||
650 | 4 | |a Journal Article | |
650 | 4 | |a Anakinra | |
650 | 4 | |a COVID-19 | |
650 | 4 | |a Immunomodulators | |
650 | 4 | |a Interleukin-1 (IL-1) receptor antagonists | |
650 | 4 | |a SARS-CoV-2 infection | |
650 | 7 | |a Interleukin 1 Receptor Antagonist Protein |2 NLM | |
650 | 7 | |a Receptors, Interleukin-1 |2 NLM | |
773 | 0 | 8 | |i Enthalten in |t Drugs of today (Barcelona, Spain : 1998) |d 1998 |g 59(2023), 3 vom: 05. März, Seite 107-112 |w (DE-627)NLM123139600 |x 1699-3993 |7 nnns |
773 | 1 | 8 | |g volume:59 |g year:2023 |g number:3 |g day:05 |g month:03 |g pages:107-112 |
856 | 4 | 0 | |u http://dx.doi.org/10.1358/dot.2023.59.3.3542446 |3 Volltext |
912 | |a GBV_USEFLAG_A | ||
912 | |a GBV_NLM | ||
951 | |a AR | ||
952 | |d 59 |j 2023 |e 3 |b 05 |c 03 |h 107-112 |