SARS-CoV-2-specific humoral and cellular immunity in two renal transplants and two hemodialysis patients treated with convalescent plasma.
Aged
Aged, 80 and over
Antibodies, Neutralizing
/ blood
Antibodies, Viral
/ blood
Antiviral Agents
/ therapeutic use
C-Reactive Protein
COVID-19
/ immunology
Enzyme-Linked Immunospot Assay
/ methods
Female
Humans
Immunity, Cellular
/ immunology
Immunity, Humoral
/ immunology
Immunization, Passive
/ methods
Immunoglobulin G
/ blood
Kidney Transplantation
Middle Aged
Renal Dialysis
SARS-CoV-2
/ immunology
Spike Glycoprotein, Coronavirus
/ immunology
COVID-19 Serotherapy
COVID-19 Drug Treatment
COVID-19
ELISpot
cellular immunity
convalescent plasma
hemodialysis
kidney transplantation
Journal
Journal of medical virology
ISSN: 1096-9071
Titre abrégé: J Med Virol
Pays: United States
ID NLM: 7705876
Informations de publication
Date de publication:
05 2021
05 2021
Historique:
revised:
22
01
2021
received:
08
12
2020
accepted:
29
01
2021
pubmed:
3
2
2021
medline:
4
5
2021
entrez:
2
2
2021
Statut:
ppublish
Résumé
When patients with chronic kidney disease are infected with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) they can face two specific problems: virus-specific immune responses may be impaired and remdesivir, an antiviral drug described to shorten recovery, is contraindicated. Antiviral treatment with convalescent plasma (CP) could be an alternative treatment option. In this case report, we present two kidney transplant recipients and two hemodialysis patients who were infected with SARS-CoV-2 and received CP. Antibodies against the receptor-binding domain in the S1 subunit of the SARS-CoV-2 spike protein were determined sequentially by immunoglobulin G (IgG) enzyme-linked immunosorbent assay (ELISA) and neutralization assay and specific cellular responses by interferon-gamma ELISpot. Before treatment, in both kidney transplant recipients and one hemodialysis patient antibodies were undetectable by ELISA (ratio < 1.1), corresponding to low neutralizing antibody titers (≤1:40). ELISpot responses in the four patients were either weak or absent. After CP treatment, we observed an increase of SARS-CoV-2-specific antibodies (IgG ratio and neutralization titer) and of specific cellular responses. After intermittent clinical improvement, one kidney transplant recipient again developed typical symptoms on Day 12 after treatment and received a second cycle of CP treatment. Altogether, three patients clinically improved and could be discharged from the hospital. However, one 83-year-old multimorbid patient deceased. Our data suggest that the success of CP therapy may only be temporary in patients with chronic kidney disease; which requires close monitoring of viral load and antiviral immunity and possibly an adaptation of the treatment regimen.
Identifiants
pubmed: 33527424
doi: 10.1002/jmv.26840
pmc: PMC8014298
doi:
Substances chimiques
Antibodies, Neutralizing
0
Antibodies, Viral
0
Antiviral Agents
0
Immunoglobulin G
0
Spike Glycoprotein, Coronavirus
0
spike protein, SARS-CoV-2
0
C-Reactive Protein
9007-41-4
Types de publication
Case Reports
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
3047-3054Subventions
Organisme : Rudolf Ackermann Foundation
ID : Grant to O.W.
Organisme : Stiftung Universitätsmedizin Essen
ID : Grant to A.K.
Informations de copyright
© 2021 The Authors. Journal of Medical Virology published by Wiley Periodicals LLC.
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