Does methotrexate influence COVID-19 infection? Case series and mechanistic data.


Journal

Arthritis research & therapy
ISSN: 1478-6362
Titre abrégé: Arthritis Res Ther
Pays: England
ID NLM: 101154438

Informations de publication

Date de publication:
10 06 2021
Historique:
received: 07 10 2020
accepted: 22 02 2021
entrez: 11 6 2021
pubmed: 12 6 2021
medline: 22 6 2021
Statut: epublish

Résumé

To investigate whether methotrexate treatment may affect the susceptibility to infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Clinical assessment of symptoms, SARS-CoV-2 RNA, and anti-SARS-CoV-2 IgG in an initial case series of four families and confirmatory case series of seven families, within which one family member developed coronavirus disease 19 (COVID-19) and exposed another family member receiving methotrexate treatment; experimental part with methotrexate treatment of mice and organoids followed by the assessment of mRNA and protein expression of the SARS-CoV-2 receptor angiotensin-converting enzyme (ACE)-2. In the initial case series, three of four women on a joint ski trip developed COVID-19, while the fourth woman, under treatment with methotrexate, remained virus-free. Two of the three diseased women infected their husbands, while the third husband treated with methotrexate remained virus-free. In addition, 7 other families were identified in a follow-up case series, in which one member developed COVID-19, while the other, receiving methotrexate, remained healthy. Experimentally, when mice were treated with methotrexate, ACE2 expression significantly decreased in the lung, in the intestinal epithelium, and in intestinal organoids. These clinical and experimental data indicate that methotrexate has certain protective effects on SARS-CoV-2 infection via downregulating ACE2.

Sections du résumé

BACKGROUND
To investigate whether methotrexate treatment may affect the susceptibility to infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2).
METHODS
Clinical assessment of symptoms, SARS-CoV-2 RNA, and anti-SARS-CoV-2 IgG in an initial case series of four families and confirmatory case series of seven families, within which one family member developed coronavirus disease 19 (COVID-19) and exposed another family member receiving methotrexate treatment; experimental part with methotrexate treatment of mice and organoids followed by the assessment of mRNA and protein expression of the SARS-CoV-2 receptor angiotensin-converting enzyme (ACE)-2.
RESULTS
In the initial case series, three of four women on a joint ski trip developed COVID-19, while the fourth woman, under treatment with methotrexate, remained virus-free. Two of the three diseased women infected their husbands, while the third husband treated with methotrexate remained virus-free. In addition, 7 other families were identified in a follow-up case series, in which one member developed COVID-19, while the other, receiving methotrexate, remained healthy. Experimentally, when mice were treated with methotrexate, ACE2 expression significantly decreased in the lung, in the intestinal epithelium, and in intestinal organoids.
CONCLUSION
These clinical and experimental data indicate that methotrexate has certain protective effects on SARS-CoV-2 infection via downregulating ACE2.

Identifiants

pubmed: 34112217
doi: 10.1186/s13075-021-02464-4
pii: 10.1186/s13075-021-02464-4
pmc: PMC8190723
doi:

Substances chimiques

RNA, Viral 0
Methotrexate YL5FZ2Y5U1

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

166

Références

Nat Commun. 2019 Apr 23;10(1):1916
pubmed: 31015489
Arthritis Rheumatol. 2020 Dec;72(12):1981-1989
pubmed: 32725762
Reprod Sci. 2016 Feb;23(2):200-10
pubmed: 26243544
Nat Rev Immunol. 2020 May;20(5):271-272
pubmed: 32296135
Nephrol Dial Transplant. 2012 May;27(5):1793-800
pubmed: 22036945
Circ Res. 2016 Apr 15;118(8):1313-26
pubmed: 27081112
Nat Commun. 2020 Apr 24;11(1):1995
pubmed: 32332732
EBioMedicine. 2020 Aug;58:102925
pubmed: 32745993
Cell. 2020 Apr 16;181(2):271-280.e8
pubmed: 32142651
Cell. 2020 May 14;181(4):905-913.e7
pubmed: 32333836
Arthritis Res Ther. 2018 May 30;20(1):103
pubmed: 29848356
PLoS One. 2014 Apr 18;9(4):e95382
pubmed: 24748324
Arthritis Rheum. 2004 May;50(5):1370-82
pubmed: 15146406
Lancet. 2020 Feb 15;395(10223):497-506
pubmed: 31986264
Nat Rev Rheumatol. 2020 Mar;16(3):145-154
pubmed: 32066940
Ann Rheum Dis. 2020 Jul;79(7):859-866
pubmed: 32471903
N Engl J Med. 2020 Jul 2;383(1):85-88
pubmed: 32348641
Nat Commun. 2020 Jul 24;11(1):3774
pubmed: 32709909
Int J Clin Pharmacol Res. 1989;9(3):209-15
pubmed: 2545638
J Virol. 2004 Oct;78(20):11429-33
pubmed: 15452268

Auteurs

Fabian Schälter (F)

Department of Internal Medicine 3, Friedrich-Alexander University (FAU) Erlangen-Nürnberg and Universitätsklinikum Erlangen, Erlangen, Germany.
Deutsches Zentrum fuer Immuntherapie (DZI), Friedrich-Alexander University (FAU) Erlangen-Nürnberg and Universitätsklinikum Erlangen, Erlangen, Germany.

Kerstin Dürholz (K)

Department of Internal Medicine 3, Friedrich-Alexander University (FAU) Erlangen-Nürnberg and Universitätsklinikum Erlangen, Erlangen, Germany.
Deutsches Zentrum fuer Immuntherapie (DZI), Friedrich-Alexander University (FAU) Erlangen-Nürnberg and Universitätsklinikum Erlangen, Erlangen, Germany.

Laura Bucci (L)

Department of Internal Medicine 3, Friedrich-Alexander University (FAU) Erlangen-Nürnberg and Universitätsklinikum Erlangen, Erlangen, Germany.
Deutsches Zentrum fuer Immuntherapie (DZI), Friedrich-Alexander University (FAU) Erlangen-Nürnberg and Universitätsklinikum Erlangen, Erlangen, Germany.

Gerd Burmester (G)

Department of Rheumatology and Clinical Immunology, Charité, Berlin, Germany.

Roberto Caporali (R)

Department of Clinical Sciences and Community Health, Research Center for Adult and Pediatric Rheumatic Diseases, University of Milan, G. Pini Hospital, Milan, Italy.

Camille Figuereido (C)

Cobra Clinic of Rheumatology and Research Center, São Paulo, Brazil.
Department of Rheumatology, University of Sao Paulo, São Paulo, Brazil.

Jaime Fogagnolo Cobra (JF)

Cobra Clinic of Rheumatology and Research Center, São Paulo, Brazil.
Department of Rheumatology, University of Sao Paulo, São Paulo, Brazil.

Bernhard Manger (B)

Department of Internal Medicine 3, Friedrich-Alexander University (FAU) Erlangen-Nürnberg and Universitätsklinikum Erlangen, Erlangen, Germany.
Deutsches Zentrum fuer Immuntherapie (DZI), Friedrich-Alexander University (FAU) Erlangen-Nürnberg and Universitätsklinikum Erlangen, Erlangen, Germany.

Mario M Zaiss (MM)

Department of Internal Medicine 3, Friedrich-Alexander University (FAU) Erlangen-Nürnberg and Universitätsklinikum Erlangen, Erlangen, Germany.
Deutsches Zentrum fuer Immuntherapie (DZI), Friedrich-Alexander University (FAU) Erlangen-Nürnberg and Universitätsklinikum Erlangen, Erlangen, Germany.

Georg Schett (G)

Department of Internal Medicine 3, Friedrich-Alexander University (FAU) Erlangen-Nürnberg and Universitätsklinikum Erlangen, Erlangen, Germany. georg.schett@uk-erlangen.de.
Deutsches Zentrum fuer Immuntherapie (DZI), Friedrich-Alexander University (FAU) Erlangen-Nürnberg and Universitätsklinikum Erlangen, Erlangen, Germany. georg.schett@uk-erlangen.de.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH