SARS-CoV-2 antibody dynamics and B-cell memory response over time in COVID-19 convalescent subjects.


Journal

Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases
ISSN: 1469-0691
Titre abrégé: Clin Microbiol Infect
Pays: England
ID NLM: 9516420

Informations de publication

Date de publication:
Sep 2021
Historique:
received: 23 02 2021
revised: 24 04 2021
accepted: 01 05 2021
pubmed: 12 5 2021
medline: 14 9 2021
entrez: 11 5 2021
Statut: ppublish

Résumé

The worldwide spread of coronavirus disease 2019 (COVID-19) highlights the need for assessment of long-term humoral immunity in convalescent subjects. Our objectives were to evaluate long-term IgG antibody response to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and B-cell memory response in COVID-19 convalescent subjects. Blood samples were collected from a cohort of subjects recovering from COVID-19 and from healthy subjects who donated blood. SARS-CoV-2 IgG antibodies were quantitatively detected by ELISA using anti-S1 spike IgG. SARS-CoV-2 spike-specific IgG memory B cells were evaluated by reversed B-cell FluroSpot based on human IgG SARS-CoV-2 receptor-binding domain in a randomly selected group of subjects recovering from COVID-19. Statistical analysis was performed with clinical variables and time post COVID-19 infection. Antibody response was not detected in 26 of 392 COVID-19 convalescent subjects (6.6%). Over a period of 9 months, the level of antibodies decreased by 50% but stabilized at 6 months, and a protective level prevailed for up to 9 months. No differences were found regarding IgG SARS-CoV-2 antibody levels for age, gender, and major blood types over time. Over time, asymptomatic COVID-19 subjects did not differ in antibody level from subjects with mild to severe disease. Repeated paired IgG SARS-CoV-2 antibody level analyses disclosed that, over 6 and 9 months, 15.3% (nine of 59) and 15.8% (three of 19) of subjects became SARS-CoV-2 IgG-seronegative, respectively, all with a low antibody level at 3 months. Rate of antibody decline was not affected by age, gender, or clinical symptomatology. In a subgroup of recovering subjects, memory B-cell response up to 9 months post-COVID-19 infection was undetectable in 31.8% of subjects (14/44), and there was no correlation with age, SARS-CoV-2 antibody level, or time post infection. The majority of convalescent COVID-19 subjects develop an IgG SARS-CoV-2 antibody response and a protective level prevails over a period of up to 9 months, regardless of age, gender, major blood types or clinical symptomatology.

Identifiants

pubmed: 33975009
pii: S1198-743X(21)00229-9
doi: 10.1016/j.cmi.2021.05.008
pmc: PMC8106530
pii:
doi:

Substances chimiques

Antibodies, Viral 0
Immunoglobulin G 0
Spike Glycoprotein, Coronavirus 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1349.e1-1349.e6

Informations de copyright

Copyright © 2021 European Society of Clinical Microbiology and Infectious Diseases. Published by Elsevier Ltd. All rights reserved.

Auteurs

Anat Achiron (A)

Laura Schwarz-Kipp Research of Autoimmune Diseases, Sackler School of Medicine Tel-Aviv University, Neuroimmunology Laboratory at the Multiple Sclerosis Centre, Blood Bank, Sheba Medical Centre, Ramat-Gann, Israel. Electronic address: anat.achiron@sheba.health.gov.il.

Michael Gurevich (M)

Laura Schwarz-Kipp Research of Autoimmune Diseases, Sackler School of Medicine Tel-Aviv University, Neuroimmunology Laboratory at the Multiple Sclerosis Centre, Blood Bank, Sheba Medical Centre, Ramat-Gann, Israel.

Rina Falb (R)

Laura Schwarz-Kipp Research of Autoimmune Diseases, Sackler School of Medicine Tel-Aviv University, Neuroimmunology Laboratory at the Multiple Sclerosis Centre, Blood Bank, Sheba Medical Centre, Ramat-Gann, Israel.

Sapir Dreyer-Alster (S)

Laura Schwarz-Kipp Research of Autoimmune Diseases, Sackler School of Medicine Tel-Aviv University, Neuroimmunology Laboratory at the Multiple Sclerosis Centre, Blood Bank, Sheba Medical Centre, Ramat-Gann, Israel.

Polina Sonis (P)

Laura Schwarz-Kipp Research of Autoimmune Diseases, Sackler School of Medicine Tel-Aviv University, Neuroimmunology Laboratory at the Multiple Sclerosis Centre, Blood Bank, Sheba Medical Centre, Ramat-Gann, Israel.

Mathilda Mandel (M)

Laura Schwarz-Kipp Research of Autoimmune Diseases, Sackler School of Medicine Tel-Aviv University, Neuroimmunology Laboratory at the Multiple Sclerosis Centre, Blood Bank, Sheba Medical Centre, Ramat-Gann, Israel.

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Classifications MeSH