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Association between anti-interferon-alpha autoantibodies and COVID-19 in systemic lupus erythematosus
OBJECTIVES: Anti-type I interferon (IFN) autoantibodies have been reported in patients with systemic lupus erythematosus (SLE). Recently, an association of these autoantibodies with severe COVID-19 was reported in the general population. We assessed whether having pre-existing anti-IFNα autoantibodi...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7658959/ https://www.ncbi.nlm.nih.gov/pubmed/33184616 http://dx.doi.org/10.1101/2020.10.29.20222000 |
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author | Gupta, Sarthak Nakabo, Shuichiro Chu, Jun Hasni, Sarfaraz Kaplan, Mariana J. |
author_facet | Gupta, Sarthak Nakabo, Shuichiro Chu, Jun Hasni, Sarfaraz Kaplan, Mariana J. |
author_sort | Gupta, Sarthak |
collection | PubMed |
description | OBJECTIVES: Anti-type I interferon (IFN) autoantibodies have been reported in patients with systemic lupus erythematosus (SLE). Recently, an association of these autoantibodies with severe COVID-19 was reported in the general population. We assessed whether having pre-existing anti-IFNα autoantibodies was associated with COVID-19 infection in SLE patients. METHODS: Patients with SLE who developed COVID-19 between April 1(st) to October 1(st), 2020 were studied. Biobanked pre-COVID-19 plasma from these SLE subjects and healthy controls were tested for anti-IFNα IgG autoantibodies by ELISA. The ability of plasma anti-IFNα autoantibodies to block signal transducer and activator of transcription 1 (STAT1) phosphorylation by recombinant human IFNα in vitro was assessed by flow cytometry. RESULTS: Ten SLE subjects with COVID-19 were identified. A 40% of these subjects had stable autoantibodies against IFNα for up to three years preceding COVID-19 diagnosis. A 50% of the subjects with these autoantibodies neutralized IFNα induced STAT1 phosphorylation. None of the other SLE samples blocked IFNα signaling. CONCLUSIONS: We noted an increased prevalence of pre-existing anti-IFNα autoantibodies in SLE patients with COVID-19 compared to the reported prevalence in lupus patients and the general population with severe COVID-19. Autoantibodies against IFNα in SLE patients may be pathogenic and patients with them maybe at-risk of developing COVID-19. |
format | Online Article Text |
id | pubmed-7658959 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-76589592020-11-13 Association between anti-interferon-alpha autoantibodies and COVID-19 in systemic lupus erythematosus Gupta, Sarthak Nakabo, Shuichiro Chu, Jun Hasni, Sarfaraz Kaplan, Mariana J. medRxiv Article OBJECTIVES: Anti-type I interferon (IFN) autoantibodies have been reported in patients with systemic lupus erythematosus (SLE). Recently, an association of these autoantibodies with severe COVID-19 was reported in the general population. We assessed whether having pre-existing anti-IFNα autoantibodies was associated with COVID-19 infection in SLE patients. METHODS: Patients with SLE who developed COVID-19 between April 1(st) to October 1(st), 2020 were studied. Biobanked pre-COVID-19 plasma from these SLE subjects and healthy controls were tested for anti-IFNα IgG autoantibodies by ELISA. The ability of plasma anti-IFNα autoantibodies to block signal transducer and activator of transcription 1 (STAT1) phosphorylation by recombinant human IFNα in vitro was assessed by flow cytometry. RESULTS: Ten SLE subjects with COVID-19 were identified. A 40% of these subjects had stable autoantibodies against IFNα for up to three years preceding COVID-19 diagnosis. A 50% of the subjects with these autoantibodies neutralized IFNα induced STAT1 phosphorylation. None of the other SLE samples blocked IFNα signaling. CONCLUSIONS: We noted an increased prevalence of pre-existing anti-IFNα autoantibodies in SLE patients with COVID-19 compared to the reported prevalence in lupus patients and the general population with severe COVID-19. Autoantibodies against IFNα in SLE patients may be pathogenic and patients with them maybe at-risk of developing COVID-19. Cold Spring Harbor Laboratory 2020-11-03 /pmc/articles/PMC7658959/ /pubmed/33184616 http://dx.doi.org/10.1101/2020.10.29.20222000 Text en https://creativecommons.org/publicdomain/zero/1.0/This article is a US Government work. It is not subject to copyright under 17 USC 105 and is also made available for use under a CC0 license (https://creativecommons.org/publicdomain/zero/1.0/) . |
spellingShingle | Article Gupta, Sarthak Nakabo, Shuichiro Chu, Jun Hasni, Sarfaraz Kaplan, Mariana J. Association between anti-interferon-alpha autoantibodies and COVID-19 in systemic lupus erythematosus |
title | Association between anti-interferon-alpha autoantibodies and COVID-19 in systemic lupus erythematosus |
title_full | Association between anti-interferon-alpha autoantibodies and COVID-19 in systemic lupus erythematosus |
title_fullStr | Association between anti-interferon-alpha autoantibodies and COVID-19 in systemic lupus erythematosus |
title_full_unstemmed | Association between anti-interferon-alpha autoantibodies and COVID-19 in systemic lupus erythematosus |
title_short | Association between anti-interferon-alpha autoantibodies and COVID-19 in systemic lupus erythematosus |
title_sort | association between anti-interferon-alpha autoantibodies and covid-19 in systemic lupus erythematosus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7658959/ https://www.ncbi.nlm.nih.gov/pubmed/33184616 http://dx.doi.org/10.1101/2020.10.29.20222000 |
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