COVID-19 survival associates with the immunoglobulin response to the SARS-CoV-2 spike receptor binding domain.
Adaptive immunity
COVID-19
Immunoglobulins
Immunology
Influenza
Journal
The Journal of clinical investigation
ISSN: 1558-8238
Titre abrégé: J Clin Invest
Pays: United States
ID NLM: 7802877
Informations de publication
Date de publication:
01 12 2020
01 12 2020
Historique:
received:
29
07
2020
accepted:
02
09
2020
pubmed:
30
9
2020
medline:
15
12
2020
entrez:
29
9
2020
Statut:
ppublish
Résumé
BACKGROUNDSerological assays are of critical importance to investigate correlates of response and protection in coronavirus disease 2019 (COVID-19), to define previous exposure to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in populations, and to verify the development of an adaptive immune response in infected individuals.METHODSWe studied 509 patients confirmed to have COVID-19 from the San Raffaele Hospital of Milan and 480 samples of prepandemic organ donor sera collected in 2010-2012. Using fluid-phase luciferase immune precipitation (LIPS) assays, we characterized IgG, IgM, and IgA antibodies to the spike receptor binding domain (RBD), S1+S2, nucleocapsid, and ORF6 to ORF10 of SARS-CoV-2, to the HCoV-OC43 and HCoV-HKU1 betacoronaviruses spike S2, and the H1N1Ca2009 flu virus hemagglutinin. Sequential samples at 1 and 3 months after hospital discharge were also tested for SARS-CoV-2 RBD antibodies in 95 patients.RESULTSAntibodies developed rapidly against multiple SARS-CoV-2 antigens in 95% of patients by 4 weeks after symptom onset and IgG to the RBD increased until the third month of follow-up. We observed a major synchronous expansion of antibodies to the HCoV-OC43 and HCoV-HKU1 spike S2. A likely coinfection with influenza was neither linked to a more severe presentation of the disease nor to a worse outcome. Of the measured antibody responses, positivity for IgG against the SARS-CoV-2 spike RBD was predictive of survival.CONCLUSIONThe measurement of antibodies to selected epitopes of SARS-CoV-2 antigens can offer a more accurate assessment of the humoral response in patients and its impact on survival. The presence of partially cross-reactive antibodies with other betacoronaviruses is likely to impact on serological assay specificity and interpretation.TRIAL REGISTRATIONCOVID-19 Patients Characterization, Biobank, Treatment Response and Outcome Predictor (COVID-BioB). ClinicalTrials.gov identifier: NCT04318366.FUNDINGIRCCS Ospedale San Raffaele and Università Vita Salute San Raffaele.
Identifiants
pubmed: 32991329
pii: 142804
doi: 10.1172/JCI142804
pmc: PMC7685720
doi:
pii:
Substances chimiques
Antibodies, Viral
0
Antigens, Viral
0
Epitopes
0
Spike Glycoprotein, Coronavirus
0
spike protein, SARS-CoV-2
0
Banques de données
ClinicalTrials.gov
['NCT04318366']
Types de publication
Clinical Trial
Journal Article
Multicenter Study
Langues
eng
Sous-ensembles de citation
IM
Pagination
6366-6378Commentaires et corrections
Type : CommentIn
Références
N Engl J Med. 2020 Feb 20;382(8):727-733
pubmed: 31978945
Clin Chem. 2019 Sep;65(9):1141-1152
pubmed: 31409598
Nat Med. 2020 Jun;26(6):845-848
pubmed: 32350462
Clin Infect Dis. 2020 Jul 28;71(15):778-785
pubmed: 32198501
Diabetes. 2016 Jun;65(6):1690-8
pubmed: 26953162
Nature. 2020 May;581(7807):221-224
pubmed: 32225175
Immunotherapy. 2020 Dec;12(17):1247-1255
pubmed: 32900263
Diabetologia. 2017 Sep;60(9):1834-1835
pubmed: 28725911
Acta Diabetol. 2018 Mar;55(3):263-270
pubmed: 29305766
Front Immunol. 2020 May 15;11:1049
pubmed: 32574261
Eur J Immunol. 2020 Aug;50(8):1234-1236
pubmed: 32584420
Clin Infect Dis. 2020 Nov 19;71(16):2027-2034
pubmed: 32221519
Can J Infect Dis Med Microbiol. 2006 Nov;17(6):330-6
pubmed: 18382647
Lancet Respir Med. 2020 Jul;8(7):687-695
pubmed: 32386571
J Clin Microbiol. 2020 Jul 23;58(8):
pubmed: 32513859
Int J Infect Dis. 2020 May;94:49-52
pubmed: 32251798
J Infect Dis. 2020 Jun 29;222(2):206-213
pubmed: 32427334
Biom J. 2015 Mar;57(2):304-20
pubmed: 25537143
Clin Vaccine Immunol. 2009 Mar;16(3):366-71
pubmed: 19129469
Cochrane Database Syst Rev. 2020 Jun 25;6:CD013652
pubmed: 32584464
Emerg Infect Dis. 2019 Oct;25(10):1868-1877
pubmed: 31423970
PLoS One. 2011;6(8):e22576
pubmed: 21829634
Nat Med. 2020 Jul;26(7):1033-1036
pubmed: 32398876
J Infect. 2020 Jul;81(1):147-178
pubmed: 32209385
Nat Med. 2020 Aug;26(8):1200-1204
pubmed: 32555424
Cell. 2020 Jun 25;181(7):1489-1501.e15
pubmed: 32473127
Biomed Microdevices. 2011 Dec;13(6):1053-62
pubmed: 21826483
Front Immunol. 2017 Aug 16;8:976
pubmed: 28861084
J Autoimmun. 2017 Sep;83:12-21
pubmed: 28479213
Transbound Emerg Dis. 2021 Mar;68(2):253-257
pubmed: 32536002
J Infect. 2013 Aug;67(2):130-40
pubmed: 23583636
J Virol. 2020 Mar 17;94(7):
pubmed: 31996437
J Clin Microbiol. 2004 Dec;42(12):5885-8
pubmed: 15583332
Nature. 2020 Nov;587(7833):270-274
pubmed: 32726801
Eur Respir J. 2020 Aug 27;56(2):
pubmed: 32430429
Crit Care Resusc. 2020 Apr 01;22(2):91-94
pubmed: 32227819
J Immunol Methods. 2006 Jul 31;314(1-2):170-3
pubmed: 16843481
Sci Transl Med. 2020 Sep 2;12(559):
pubmed: 32817357
J Clin Immunol. 2021 Jul;41(5):906-913
pubmed: 33725211
PLoS One. 2013 Nov 08;8(11):e78664
pubmed: 24250806
J Infect Dis. 2005 Jun 15;191(12):2033-7
pubmed: 15897988
J Clin Virol. 2020 Aug;129:104480
pubmed: 32505777
Lancet Infect Dis. 2020 Jul;20(7):758-759
pubmed: 32330441
J Clin Microbiol. 2020 May 26;58(6):
pubmed: 32229605
Lancet Infect Dis. 2020 May;20(5):565-574
pubmed: 32213337
Emerg Infect Dis. 2020 Jul;26(7):1478-1488
pubmed: 32267220
Clin Diagn Lab Immunol. 2005 Nov;12(11):1317-21
pubmed: 16275947
Clin Transl Gastroenterol. 2017 Jan 19;8(1):e215
pubmed: 28102858
Science. 2020 Aug 7;369(6504):643-650
pubmed: 32540902
Clin Immunol. 2020 Aug;217:108509
pubmed: 32535188
mBio. 2020 Sep 25;11(5):
pubmed: 32978311