Interferon-α2 Auto-antibodies in Convalescent Plasma Therapy for COVID-19
Purpose To study the effect of interferon-α2 auto-antibodies (IFN-α2 Abs) on clinical and virological outcomes in critically ill COVID-19 patients and the risk of IFN-α2 Abs transfer during convalescent plasma treatment. Methods Sera from healthy controls, cases of COVID-19, and other respiratory il...
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| Veröffentlicht in: | Journal of clinical immunology Jg. 42; H. 2; S. 232 - 239 |
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| Sprache: | Englisch |
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New York
Springer US
01.02.2022
Springer Nature B.V |
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| ISSN: | 0271-9142, 1573-2592, 1573-2592 |
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| Abstract | Purpose
To study the effect of interferon-α2 auto-antibodies (IFN-α2 Abs) on clinical and virological outcomes in critically ill COVID-19 patients and the risk of IFN-α2 Abs transfer during convalescent plasma treatment.
Methods
Sera from healthy controls, cases of COVID-19, and other respiratory illness were tested for IFN-α2 Abs by ELISA and a pseudo virus–based neutralization assay. The effects of disease severity, sex, and age on the risk of having neutralizing IFN-α2 Abs were determined. Longitudinal analyses were performed to determine association between IFN-α2 Abs and survival and viral load and whether serum IFN-α2 Abs appeared after convalescent plasma transfusion.
Results
IFN-α2 neutralizing sera were found only in COVID-19 patients, with proportions increasing with disease severity and age. In the acute stage of COVID-19, all sera from patients with ELISA-detected IFN-α2 Abs (13/164, 7.9%) neutralized levels of IFN-α2 exceeding physiological concentrations found in human plasma and this was associated with delayed viral clearance. Convalescent plasma donors that were anti-IFN-α2 ELISA positive (3/118, 2.5%) did not neutralize the same levels of IFN-α2. Neutralizing serum IFN-α2 Abs were associated with delayed viral clearance from the respiratory tract.
Conclusions
IFN-α2 Abs were detected by ELISA and neutralization assay in COVID-19 patients, but not in ICU patients with other respiratory illnesses. The presence of neutralizing IFN-α2 Abs in critically ill COVID-19 is associated with delayed viral clearance. IFN-α2 Abs in COVID-19 convalescent plasma donors were not neutralizing in the conditions tested. |
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| AbstractList | To study the effect of interferon-α2 auto-antibodies (IFN-α2 Abs) on clinical and virological outcomes in critically ill COVID-19 patients and the risk of IFN-α2 Abs transfer during convalescent plasma treatment.
Sera from healthy controls, cases of COVID-19, and other respiratory illness were tested for IFN-α2 Abs by ELISA and a pseudo virus-based neutralization assay. The effects of disease severity, sex, and age on the risk of having neutralizing IFN-α2 Abs were determined. Longitudinal analyses were performed to determine association between IFN-α2 Abs and survival and viral load and whether serum IFN-α2 Abs appeared after convalescent plasma transfusion.
IFN-α2 neutralizing sera were found only in COVID-19 patients, with proportions increasing with disease severity and age. In the acute stage of COVID-19, all sera from patients with ELISA-detected IFN-α2 Abs (13/164, 7.9%) neutralized levels of IFN-α2 exceeding physiological concentrations found in human plasma and this was associated with delayed viral clearance. Convalescent plasma donors that were anti-IFN-α2 ELISA positive (3/118, 2.5%) did not neutralize the same levels of IFN-α2. Neutralizing serum IFN-α2 Abs were associated with delayed viral clearance from the respiratory tract.
IFN-α2 Abs were detected by ELISA and neutralization assay in COVID-19 patients, but not in ICU patients with other respiratory illnesses. The presence of neutralizing IFN-α2 Abs in critically ill COVID-19 is associated with delayed viral clearance. IFN-α2 Abs in COVID-19 convalescent plasma donors were not neutralizing in the conditions tested. Abstract PurposeTo study the effect of interferon-α2 auto-antibodies (IFN-α2 Abs) on clinical and virological outcomes in critically ill COVID-19 patients and the risk of IFN-α2 Abs transfer during convalescent plasma treatment.MethodsSera from healthy controls, cases of COVID-19, and other respiratory illness were tested for IFN-α2 Abs by ELISA and a pseudo virus–based neutralization assay. The effects of disease severity, sex, and age on the risk of having neutralizing IFN-α2 Abs were determined. Longitudinal analyses were performed to determine association between IFN-α2 Abs and survival and viral load and whether serum IFN-α2 Abs appeared after convalescent plasma transfusion.ResultsIFN-α2 neutralizing sera were found only in COVID-19 patients, with proportions increasing with disease severity and age. In the acute stage of COVID-19, all sera from patients with ELISA-detected IFN-α2 Abs (13/164, 7.9%) neutralized levels of IFN-α2 exceeding physiological concentrations found in human plasma and this was associated with delayed viral clearance. Convalescent plasma donors that were anti-IFN-α2 ELISA positive (3/118, 2.5%) did not neutralize the same levels of IFN-α2. Neutralizing serum IFN-α2 Abs were associated with delayed viral clearance from the respiratory tract.ConclusionsIFN-α2 Abs were detected by ELISA and neutralization assay in COVID-19 patients, but not in ICU patients with other respiratory illnesses. The presence of neutralizing IFN-α2 Abs in critically ill COVID-19 is associated with delayed viral clearance. IFN-α2 Abs in COVID-19 convalescent plasma donors were not neutralizing in the conditions tested. To study the effect of interferon-α2 auto-antibodies (IFN-α2 Abs) on clinical and virological outcomes in critically ill COVID-19 patients and the risk of IFN-α2 Abs transfer during convalescent plasma treatment.PURPOSETo study the effect of interferon-α2 auto-antibodies (IFN-α2 Abs) on clinical and virological outcomes in critically ill COVID-19 patients and the risk of IFN-α2 Abs transfer during convalescent plasma treatment.Sera from healthy controls, cases of COVID-19, and other respiratory illness were tested for IFN-α2 Abs by ELISA and a pseudo virus-based neutralization assay. The effects of disease severity, sex, and age on the risk of having neutralizing IFN-α2 Abs were determined. Longitudinal analyses were performed to determine association between IFN-α2 Abs and survival and viral load and whether serum IFN-α2 Abs appeared after convalescent plasma transfusion.METHODSSera from healthy controls, cases of COVID-19, and other respiratory illness were tested for IFN-α2 Abs by ELISA and a pseudo virus-based neutralization assay. The effects of disease severity, sex, and age on the risk of having neutralizing IFN-α2 Abs were determined. Longitudinal analyses were performed to determine association between IFN-α2 Abs and survival and viral load and whether serum IFN-α2 Abs appeared after convalescent plasma transfusion.IFN-α2 neutralizing sera were found only in COVID-19 patients, with proportions increasing with disease severity and age. In the acute stage of COVID-19, all sera from patients with ELISA-detected IFN-α2 Abs (13/164, 7.9%) neutralized levels of IFN-α2 exceeding physiological concentrations found in human plasma and this was associated with delayed viral clearance. Convalescent plasma donors that were anti-IFN-α2 ELISA positive (3/118, 2.5%) did not neutralize the same levels of IFN-α2. Neutralizing serum IFN-α2 Abs were associated with delayed viral clearance from the respiratory tract.RESULTSIFN-α2 neutralizing sera were found only in COVID-19 patients, with proportions increasing with disease severity and age. In the acute stage of COVID-19, all sera from patients with ELISA-detected IFN-α2 Abs (13/164, 7.9%) neutralized levels of IFN-α2 exceeding physiological concentrations found in human plasma and this was associated with delayed viral clearance. Convalescent plasma donors that were anti-IFN-α2 ELISA positive (3/118, 2.5%) did not neutralize the same levels of IFN-α2. Neutralizing serum IFN-α2 Abs were associated with delayed viral clearance from the respiratory tract.IFN-α2 Abs were detected by ELISA and neutralization assay in COVID-19 patients, but not in ICU patients with other respiratory illnesses. The presence of neutralizing IFN-α2 Abs in critically ill COVID-19 is associated with delayed viral clearance. IFN-α2 Abs in COVID-19 convalescent plasma donors were not neutralizing in the conditions tested.CONCLUSIONSIFN-α2 Abs were detected by ELISA and neutralization assay in COVID-19 patients, but not in ICU patients with other respiratory illnesses. The presence of neutralizing IFN-α2 Abs in critically ill COVID-19 is associated with delayed viral clearance. IFN-α2 Abs in COVID-19 convalescent plasma donors were not neutralizing in the conditions tested. Purpose To study the effect of interferon-α2 auto-antibodies (IFN-α2 Abs) on clinical and virological outcomes in critically ill COVID-19 patients and the risk of IFN-α2 Abs transfer during convalescent plasma treatment. Methods Sera from healthy controls, cases of COVID-19, and other respiratory illness were tested for IFN-α2 Abs by ELISA and a pseudo virus–based neutralization assay. The effects of disease severity, sex, and age on the risk of having neutralizing IFN-α2 Abs were determined. Longitudinal analyses were performed to determine association between IFN-α2 Abs and survival and viral load and whether serum IFN-α2 Abs appeared after convalescent plasma transfusion. Results IFN-α2 neutralizing sera were found only in COVID-19 patients, with proportions increasing with disease severity and age. In the acute stage of COVID-19, all sera from patients with ELISA-detected IFN-α2 Abs (13/164, 7.9%) neutralized levels of IFN-α2 exceeding physiological concentrations found in human plasma and this was associated with delayed viral clearance. Convalescent plasma donors that were anti-IFN-α2 ELISA positive (3/118, 2.5%) did not neutralize the same levels of IFN-α2. Neutralizing serum IFN-α2 Abs were associated with delayed viral clearance from the respiratory tract. Conclusions IFN-α2 Abs were detected by ELISA and neutralization assay in COVID-19 patients, but not in ICU patients with other respiratory illnesses. The presence of neutralizing IFN-α2 Abs in critically ill COVID-19 is associated with delayed viral clearance. IFN-α2 Abs in COVID-19 convalescent plasma donors were not neutralizing in the conditions tested. |
| Author | Lamers, Mart M. GeurtsvanKessel, Corine H. Endeman, Henrik Raadsen, Matthijs P. Jordans, Carlijn C. E. van den Doel, Petra B. van den Akker, Johannes P. C. Rokx, Casper Goeijenbier, Marco Koopmans, Marion P. G. Mykytyn, Anna Z. Haagmans, Bart L. Rijnders, Bart J. A. van Gorp, Eric C. M. Gharbharan, Arvind |
| Author_xml | – sequence: 1 givenname: Matthijs P. orcidid: 0000-0002-3774-8165 surname: Raadsen fullname: Raadsen, Matthijs P. organization: Viroscience Department, Erasmus MC – sequence: 2 givenname: Arvind surname: Gharbharan fullname: Gharbharan, Arvind organization: Department of Medical Microbiology and Infectious Diseases, Erasmus MC – sequence: 3 givenname: Carlijn C. E. surname: Jordans fullname: Jordans, Carlijn C. E. organization: Department of Medical Microbiology and Infectious Diseases, Erasmus MC – sequence: 4 givenname: Anna Z. surname: Mykytyn fullname: Mykytyn, Anna Z. organization: Viroscience Department, Erasmus MC – sequence: 5 givenname: Mart M. surname: Lamers fullname: Lamers, Mart M. organization: Viroscience Department, Erasmus MC – sequence: 6 givenname: Petra B. surname: van den Doel fullname: van den Doel, Petra B. organization: Viroscience Department, Erasmus MC – sequence: 7 givenname: Henrik surname: Endeman fullname: Endeman, Henrik organization: Intensive Care Department, Erasmus MC – sequence: 8 givenname: Johannes P. C. surname: van den Akker fullname: van den Akker, Johannes P. C. organization: Intensive Care Department, Erasmus MC – sequence: 9 givenname: Corine H. surname: GeurtsvanKessel fullname: GeurtsvanKessel, Corine H. organization: Viroscience Department, Erasmus MC – sequence: 10 givenname: Marion P. G. surname: Koopmans fullname: Koopmans, Marion P. G. organization: Viroscience Department, Erasmus MC – sequence: 11 givenname: Casper surname: Rokx fullname: Rokx, Casper organization: Department of Medical Microbiology and Infectious Diseases, Erasmus MC – sequence: 12 givenname: Marco surname: Goeijenbier fullname: Goeijenbier, Marco organization: Viroscience Department, Erasmus MC, Intensive Care Department, Erasmus MC – sequence: 13 givenname: Eric C. M. surname: van Gorp fullname: van Gorp, Eric C. M. organization: Viroscience Department, Erasmus MC – sequence: 14 givenname: Bart J. A. surname: Rijnders fullname: Rijnders, Bart J. A. organization: Department of Medical Microbiology and Infectious Diseases, Erasmus MC – sequence: 15 givenname: Bart L. surname: Haagmans fullname: Haagmans, Bart L. email: b.haagmans@erasmusmc.nl organization: Viroscience Department, Erasmus MC |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/34767118$$D View this record in MEDLINE/PubMed |
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| Keywords | COVID-19 SARS-CoV-2 Convalescent plasma Auto-antibodies Interferon alpha |
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To study the effect of interferon-α2 auto-antibodies (IFN-α2 Abs) on clinical and virological outcomes in critically ill COVID-19 patients and the risk... To study the effect of interferon-α2 auto-antibodies (IFN-α2 Abs) on clinical and virological outcomes in critically ill COVID-19 patients and the risk of... Abstract PurposeTo study the effect of interferon-α2 auto-antibodies (IFN-α2 Abs) on clinical and virological outcomes in critically ill COVID-19 patients and... |
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| SubjectTerms | Adult Aged Antibodies, Neutralizing - immunology Antibodies, Viral - immunology Antiviral Agents - immunology Autoantibodies Autoantibodies - immunology Biomedical and Life Sciences Biomedicine Blood Component Transfusion - methods Coronaviruses COVID-19 COVID-19 - immunology COVID-19 - therapy COVID-19 Serotherapy Critical Illness Enzyme-linked immunosorbent assay Female Humans Immunization, Passive - methods Immunoglobulin G - immunology Immunology Infectious Diseases Interferon Interferon alpha-2 - immunology Internal Medicine Male Medical Microbiology Middle Aged Original Original Article Patients Plasma Plasma - immunology Respiratory diseases Respiratory tract SARS-CoV-2 - immunology |
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| Title | Interferon-α2 Auto-antibodies in Convalescent Plasma Therapy for COVID-19 |
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