SARS-CoV-2 Antibody Responses Correlate with Resolution of RNAemia But Are Short-Lived in Patients with Mild Illness.
Journal
medRxiv : the preprint server for health sciences
Titre abrégé: medRxiv
Pays: United States
ID NLM: 101767986
Informations de publication
Date de publication:
17 Aug 2020
17 Aug 2020
Historique:
pubmed:
26
8
2020
medline:
26
8
2020
entrez:
26
8
2020
Statut:
epublish
Résumé
SARS-CoV-2-specific antibodies, particularly those preventing viral spike receptor binding domain (RBD) interaction with host angiotensin-converting enzyme 2 (ACE2) receptor, could offer protective immunity, and may affect clinical outcomes of COVID-19 patients. We analyzed 625 serial plasma samples from 40 hospitalized COVID-19 patients and 170 SARS-CoV-2-infected outpatients and asymptomatic individuals. Severely ill patients developed significantly higher SARS-CoV-2-specific antibody responses than outpatients and asymptomatic individuals. The development of plasma antibodies was correlated with decreases in viral RNAemia, consistent with potential humoral immune clearance of virus. Using a novel competition ELISA, we detected antibodies blocking RBD-ACE2 interactions in 68% of inpatients and 40% of outpatients tested. Cross-reactive antibodies recognizing SARS-CoV RBD were found almost exclusively in hospitalized patients. Outpatient and asymptomatic individuals' serological responses to SARS-CoV-2 decreased within 2 months, suggesting that humoral protection may be short-lived.
Identifiants
pubmed: 32839786
doi: 10.1101/2020.08.15.20175794
pmc: PMC7444305
pii:
doi:
Types de publication
Preprint
Langues
eng
Déclaration de conflit d'intérêts
Competing interests: The authors declare no competing interests.
Références
Emerg Infect Dis. 2019 Oct;25(10):1868-1877
pubmed: 31423970
J Allergy Clin Immunol. 2021 Feb;147(2):545-557.e9
pubmed: 33221383
Annu Rev Virol. 2016 Sep 29;3(1):237-261
pubmed: 27578435
Nat Med. 2020 Jun;26(6):845-848
pubmed: 32350462
Cell Rep. 2020 Jun 2;31(9):107725
pubmed: 32426212
Clin Infect Dis. 2021 May 4;72(9):e291-e295
pubmed: 32965474
Nat Microbiol. 2020 Apr;5(4):536-544
pubmed: 32123347
Lancet. 2020 Feb 15;395(10223):497-506
pubmed: 31986264
Emerg Infect Dis. 2020 Jul;26(7):1478-1488
pubmed: 32267220
Lancet. 2020 Feb 15;395(10223):507-513
pubmed: 32007143
Clin Infect Dis. 2020 Nov 19;71(16):2027-2034
pubmed: 32221519
Clin Infect Dis. 2020 Nov 19;71(16):2255-2258
pubmed: 32337590
JAMA. 2020 Apr 7;323(13):1239-1242
pubmed: 32091533
Nature. 2020 Mar;579(7798):270-273
pubmed: 32015507
Science. 2020 Mar 13;367(6483):1260-1263
pubmed: 32075877
Emerg Microbes Infect. 2020 Dec;9(1):382-385
pubmed: 32065055
Nature. 2020 Aug;584(7821):437-442
pubmed: 32555388
Emerg Infect Dis. 2016 Jun;22(6):
pubmed: 27192543
Euro Surveill. 2020 Jan;25(3):
pubmed: 31992387
JAMA. 2020 May 26;323(20):2052-2059
pubmed: 32320003
JAMA. 2020 May 19;323(19):1967-1969
pubmed: 32250394
Lancet. 2020 Mar 28;395(10229):1054-1062
pubmed: 32171076
N Engl J Med. 2014 Aug 28;371(9):828-35
pubmed: 25162889
mBio. 2020 Mar 26;11(2):
pubmed: 32217609
Curr Protoc Microbiol. 2020 Jun;57(1):e100
pubmed: 32302069
Cell Mol Immunol. 2020 Jun;17(6):613-620
pubmed: 32203189
BMJ. 2020 Mar 26;368:m1091
pubmed: 32217556
J Clin Invest. 2020 Apr 1;130(4):1545-1548
pubmed: 32167489