Improved SARS-CoV-2 Neutralization of Delta and Omicron BA.1 Variants of Concern after Fourth Vaccination in Hemodialysis Patients.
COVID-19 vaccination
SARS-CoV-2
hemodialysis
in-vitro viral neutralization
Journal
Vaccines
ISSN: 2076-393X
Titre abrégé: Vaccines (Basel)
Pays: Switzerland
ID NLM: 101629355
Informations de publication
Date de publication:
16 Aug 2022
16 Aug 2022
Historique:
received:
20
07
2022
revised:
11
08
2022
accepted:
13
08
2022
entrez:
26
8
2022
pubmed:
27
8
2022
medline:
27
8
2022
Statut:
epublish
Résumé
Hemodialysis patients are exposed to a markedly increased risk when infected with SARS-CoV-2. To date, it is unclear if hemodialysis patients benefit from four vaccinations. A total of 142 hemodialysis patients received four COVID-19 vaccinations until March 2022. RDB binding antibody titers were determined in a competitive surrogate neutralization assay. Vero-E6 cells were infected with SARS-CoV-2 variants of concern (VoC), Delta (B.1.617.2), or Omicron (B.1.1.529, sub-lineage BA.1) to determine serum infection neutralization capacity. Four weeks after the fourth vaccination, serum infection neutralization capacity significantly increased from a 50% inhibitory concentration (IC50, serum dilution factor 1:x) of 247.0 (46.3−1560.8) to 2560.0 (1174.0−2560.0) for the Delta VoC, and from 37.5 (20.0−198.8) to 668.5 (182.2−2560.0) for the Omicron VoC (each p < 0.001) compared to four months after the third vaccination. A significant increase in the neutralization capacity was even observed for patients with high antibody titers after three vaccinations (p < 0.001). Ten patients with SARS-CoV-2 breakthrough infection after the first blood sampling had by trend lower prior neutralization capacity for Omicron (p = 0.051). Our findings suggest that hemodialysis patients benefit from a fourth vaccination in particular in the light of the highly infectious SARS-CoV-2 Omicron-variants. A routinely applied four-time vaccination seems to broaden immunity against variants and would be recommended in hemodialysis patients.
Identifiants
pubmed: 36016216
pii: vaccines10081328
doi: 10.3390/vaccines10081328
pmc: PMC9415993
pii:
doi:
Types de publication
Journal Article
Langues
eng
Déclaration de conflit d'intérêts
The authors declare no conflict of interest. UP is receiving grants from Hoehnle AG, SCG Cell Therapy and VirBio and personal fees from Abbott, Abbvie, Arbutus, Gilead, GSK, J&J, Roche, Sanofi, Sobi and Vaccitech. UP is co-founder and share-holder of SCG Cell Therapy.
Références
J Nephrol. 2022 Jun;35(5):1479-1487
pubmed: 35175577
Lancet Rheumatol. 2022 May;4(5):e338-e350
pubmed: 35317410
Clin J Am Soc Nephrol. 2022 Jun;17(6):872-876
pubmed: 35551070
Kidney Int. 2022 Jul;102(1):207-208
pubmed: 35580654
Toxins (Basel). 2020 May 06;12(5):
pubmed: 32384617
Kidney Int. 2022 Jun;101(6):1287-1289
pubmed: 35301007
Cell. 2022 Feb 3;185(3):457-466.e4
pubmed: 34995482
Clin J Am Soc Nephrol. 2022 Mar;17(3):395-402
pubmed: 35144970
Lancet. 2022 Feb 26;399(10327):800-802
pubmed: 35065703
Nat Commun. 2022 Jan 10;13(1):153
pubmed: 35013191
Nat Med. 2022 Mar;28(3):496-503
pubmed: 35090165
Ann Med. 2022 Dec;54(1):1511-1519
pubmed: 35594312
BMC Nephrol. 2022 May 18;23(1):189
pubmed: 35585512
Nephrol Dial Transplant. 2020 Nov 1;35(11):1973-1983
pubmed: 33151337
Emerg Infect Dis. 2022 Mar;28(3):572-581
pubmed: 35195515
Kidney Int. 2022 Jun;101(6):1289-1290
pubmed: 35421509
Nat Med. 2021 Jul;27(7):1205-1211
pubmed: 34002089
Diagnostics (Basel). 2021 Sep 24;11(10):
pubmed: 34679455
Nephrol Dial Transplant. 2021 Nov 12;:
pubmed: 34788858
Kidney Int. 2022 Feb;101(2):390-402
pubmed: 34856313