Retrospective analysis of 426 donors of a convalescent collective after mild COVID-19.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2021
Historique:
received: 27 11 2020
accepted: 11 02 2021
entrez: 23 2 2021
pubmed: 24 2 2021
medline: 4 3 2021
Statut: epublish

Résumé

The novel coronavirus disease 2019 (COVID-19), caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has spread across the world. The aim of our study was to characterize mild courses and to determine the antibody status for these patients. We initiated an appeal for convalescent plasma donations. 615 people contacted us, and we ultimately included 426 in our analyses, in whom it was possible to assume COVID-19 based on detection of specific SARS-CoV-2 antibodies or virus detection during the disease using RT-PCR. The median duration of the disease was 12 days and the most common symptoms were fatigue, cough and olfactory and gustatory dysfunction. Anti-SARS-CoV-2 IgG was detected in 82.4% of the persons and IgA antibodies were found in 73.9%. In 10.8%, no antibodies were detectable despite a positive RT-PCR result during the disease. Nevertheless, of 24 persons with asymptomatic courses of COVID-19, antibodies against SARS-CoV-2 could be detected in 23 (96%). Furthermore, there was a correlation between the duration of the disease and the detection of IgG antibodies. In addition, a correlation between the determined IgG antibodies and neutralizing antibodies was shown. In this study, we were able to describe mild COVID-19 courses and determine antibody statuses for them. It could be shown that, despite SARS-CoV-2 detection during the disease, not all individuals developed antibodies or their level of antibodies had dropped below the detection limit shortly after the end of the disease. The extent to which immunity to re-infection is given in persons with undetectable antibodies (IgG, IgA) needs to be investigated in future studies.

Sections du résumé

BACKGROUND
The novel coronavirus disease 2019 (COVID-19), caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has spread across the world. The aim of our study was to characterize mild courses and to determine the antibody status for these patients.
METHODS
We initiated an appeal for convalescent plasma donations. 615 people contacted us, and we ultimately included 426 in our analyses, in whom it was possible to assume COVID-19 based on detection of specific SARS-CoV-2 antibodies or virus detection during the disease using RT-PCR.
RESULTS
The median duration of the disease was 12 days and the most common symptoms were fatigue, cough and olfactory and gustatory dysfunction. Anti-SARS-CoV-2 IgG was detected in 82.4% of the persons and IgA antibodies were found in 73.9%. In 10.8%, no antibodies were detectable despite a positive RT-PCR result during the disease. Nevertheless, of 24 persons with asymptomatic courses of COVID-19, antibodies against SARS-CoV-2 could be detected in 23 (96%). Furthermore, there was a correlation between the duration of the disease and the detection of IgG antibodies. In addition, a correlation between the determined IgG antibodies and neutralizing antibodies was shown.
CONCLUSION
In this study, we were able to describe mild COVID-19 courses and determine antibody statuses for them. It could be shown that, despite SARS-CoV-2 detection during the disease, not all individuals developed antibodies or their level of antibodies had dropped below the detection limit shortly after the end of the disease. The extent to which immunity to re-infection is given in persons with undetectable antibodies (IgG, IgA) needs to be investigated in future studies.

Identifiants

pubmed: 33621254
doi: 10.1371/journal.pone.0247665
pii: PONE-D-20-37378
pmc: PMC7901786
doi:

Substances chimiques

Antibodies, Neutralizing 0
Antibodies, Viral 0
Immunoglobulin A 0
Immunoglobulin G 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0247665

Déclaration de conflit d'intérêts

I have read the journal’s policy and the authors of this manuscript have the following competing interests: Ingvild Birschmann received speaker’s honoraria from Aspen Germany GmbH, Bristol-Myers Squibb/Pfizer, Siemens Healthcare and CSL Behring and reimbursement for congress traveling and accommodation from aspen and performed contract research for Siemens Healthcare. Ingvild Birschmann is a member of the advisory board of LFB biomedicaments, Siemens Healthcare and CSL Behring. Tobias Flieder, Tanja Vollmer, Benjamin Müller, Jens Dreier, Bastian Fischer and Cornelius Knabbe have nothing to disclose. This does not alter our adherence to PLOS ONE policies on sharing data and materials.

Références

J Virol Methods. 2021 Feb;288:114031
pubmed: 33275926
Eur J Clin Microbiol Infect Dis. 2005 Jan;24(1):44-6
pubmed: 15616839
MMWR Morb Mortal Wkly Rep. 2020 Dec 18;69(50):1922-1924
pubmed: 33332292
Eur Arch Otorhinolaryngol. 2020 Aug;277(8):2251-2261
pubmed: 32253535
Lancet. 2020 May 16;395(10236):1569-1578
pubmed: 32423584
JAMA. 2020 Apr 28;323(16):1582-1589
pubmed: 32219428
J Med Virol. 2021 Jan;93(1):448-455
pubmed: 32603515
N Engl J Med. 2021 Feb 4;384(5):403-416
pubmed: 33378609
J Korean Med Sci. 2020 Apr 13;35(14):e149
pubmed: 32281317
Br J Haematol. 2020 Aug;190(4):e204-e208
pubmed: 32609874
Emerg Microbes Infect. 2020 Dec;9(1):1546-1553
pubmed: 32608325
Proc Natl Acad Sci U S A. 2020 Apr 28;117(17):9490-9496
pubmed: 32253318
Am J Gastroenterol. 2020 May;115(5):766-773
pubmed: 32287140
N Engl J Med. 2021 Feb 18;384(7):610-618
pubmed: 33406353
Int J Infect Dis. 2020 Jun;95:421-428
pubmed: 32289565
N Engl J Med. 2021 Feb 25;384(8):693-704
pubmed: 32678530
J Clin Invest. 2020 Jun 1;130(6):2757-2765
pubmed: 32254064
Ear Nose Throat J. 2020 Nov;99(9):569-576
pubmed: 32283980
Clin Infect Dis. 2021 Jan 27;72(2):301-308
pubmed: 33501951
BMC Infect Dis. 2020 Jul 20;20(1):526
pubmed: 32689956
JCI Insight. 2020 Aug 6;5(15):
pubmed: 32554923
J Allergy Clin Immunol. 2021 Feb;147(2):545-557.e9
pubmed: 33221383
Nat Med. 2020 Aug;26(8):1200-1204
pubmed: 32555424
Cell. 2020 Jun 25;181(7):1489-1501.e15
pubmed: 32473127
Cell Mol Immunol. 2020 Jul;17(7):773-775
pubmed: 32467617
Nat Commun. 2020 Nov 13;11(1):5761
pubmed: 33188185
Clin Chim Acta. 2020 Oct;509:220-223
pubmed: 32562665
Antivir Ther. 2018;23(7):617-622
pubmed: 29923831
N Engl J Med. 2020 Nov 5;383(19):1813-1826
pubmed: 32445440
N Engl J Med. 2021 Feb 18;384(7):619-629
pubmed: 33232588

Auteurs

Tobias Flieder (T)

Herz- und Diabeteszentrum Nordrhein-Westfalen, Universitätsklinik der Ruhr-Universität Bochum, Institut für Laboratoriums- und Transfusionsmedizin, Bad Oeynhausen, Germany.

Tanja Vollmer (T)

Herz- und Diabeteszentrum Nordrhein-Westfalen, Universitätsklinik der Ruhr-Universität Bochum, Institut für Laboratoriums- und Transfusionsmedizin, Bad Oeynhausen, Germany.

Benjamin Müller (B)

Herz- und Diabeteszentrum Nordrhein-Westfalen, Universitätsklinik der Ruhr-Universität Bochum, Institut für Laboratoriums- und Transfusionsmedizin, Bad Oeynhausen, Germany.

Jens Dreier (J)

Herz- und Diabeteszentrum Nordrhein-Westfalen, Universitätsklinik der Ruhr-Universität Bochum, Institut für Laboratoriums- und Transfusionsmedizin, Bad Oeynhausen, Germany.

Bastian Fischer (B)

Herz- und Diabeteszentrum Nordrhein-Westfalen, Universitätsklinik der Ruhr-Universität Bochum, Institut für Laboratoriums- und Transfusionsmedizin, Bad Oeynhausen, Germany.

Cornelius Knabbe (C)

Herz- und Diabeteszentrum Nordrhein-Westfalen, Universitätsklinik der Ruhr-Universität Bochum, Institut für Laboratoriums- und Transfusionsmedizin, Bad Oeynhausen, Germany.

Ingvild Birschmann (I)

Herz- und Diabeteszentrum Nordrhein-Westfalen, Universitätsklinik der Ruhr-Universität Bochum, Institut für Laboratoriums- und Transfusionsmedizin, Bad Oeynhausen, Germany.

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