Safety and Immunogenicity of SARS-CoV-2 mRNA Vaccine Booster Doses in Kidney Transplant Recipients: Results of a 12-mo Follow-up From a Prospective Observational Study.


Journal

Transplantation direct
ISSN: 2373-8731
Titre abrégé: Transplant Direct
Pays: United States
ID NLM: 101651609

Informations de publication

Date de publication:
Jun 2024
Historique:
received: 18 11 2023
revised: 20 02 2024
accepted: 10 03 2024
medline: 21 5 2024
pubmed: 21 5 2024
entrez: 21 5 2024
Statut: epublish

Résumé

Booster doses of SARS-CoV-2 mRNA vaccines are commonly used in kidney transplant recipients (KTRs). However, there is uncertainty regarding the waning of vaccination responses and immunological safety in KTRs. A total of 123 KTRs were included in the final analysis of this prospective observational cohort study. The aim was to evaluate the immunogenicity and immunological safety. SARS-CoV-2 antispike IgG antibodies and anti-HLA antibodies were measured at baseline and then at months 3, 6, and 12 after vaccination with the first booster dose (ie, the third vaccine dose). Antibodies against S1 and S2 subunits of SARS-CoV-2 were evaluated using an immunochemiluminescent assay (cutoff 9.5 AU/mL, sensitivity 91.2%, and specificity 90.2%). Anti-HLA antibodies were analyzed using single-antigen bead technology. Seroconversion was reached in 65% of KTRs previously nonresponding to 2-dose mRNA vaccination; the overall seroconversion rate 3 mo after the first booster dose was 83%. Vaccination induced a durable humoral response, and the antibody levels were stable during the 12-mo study follow-up. Higher age (exponentiated beta coefficient [e Additional booster doses of SARS-CoV-2 mRNA vaccines induce durable antibody response even in a large subset of previous nonresponders and are not associated with the risk of allosensitization. Furthermore, a signal linking COVID-19 to the development of anti-HLA antibodies was observed, and this should be confirmed and further examined (NCT05483725).

Sections du résumé

Background UNASSIGNED
Booster doses of SARS-CoV-2 mRNA vaccines are commonly used in kidney transplant recipients (KTRs). However, there is uncertainty regarding the waning of vaccination responses and immunological safety in KTRs.
Methods UNASSIGNED
A total of 123 KTRs were included in the final analysis of this prospective observational cohort study. The aim was to evaluate the immunogenicity and immunological safety. SARS-CoV-2 antispike IgG antibodies and anti-HLA antibodies were measured at baseline and then at months 3, 6, and 12 after vaccination with the first booster dose (ie, the third vaccine dose). Antibodies against S1 and S2 subunits of SARS-CoV-2 were evaluated using an immunochemiluminescent assay (cutoff 9.5 AU/mL, sensitivity 91.2%, and specificity 90.2%). Anti-HLA antibodies were analyzed using single-antigen bead technology.
Results UNASSIGNED
Seroconversion was reached in 65% of KTRs previously nonresponding to 2-dose mRNA vaccination; the overall seroconversion rate 3 mo after the first booster dose was 83%. Vaccination induced a durable humoral response, and the antibody levels were stable during the 12-mo study follow-up. Higher age (exponentiated beta coefficient [e
Conclusions UNASSIGNED
Additional booster doses of SARS-CoV-2 mRNA vaccines induce durable antibody response even in a large subset of previous nonresponders and are not associated with the risk of allosensitization. Furthermore, a signal linking COVID-19 to the development of anti-HLA antibodies was observed, and this should be confirmed and further examined (NCT05483725).

Identifiants

pubmed: 38769974
doi: 10.1097/TXD.0000000000001645
pii: TXD-2023-0196
pmc: PMC11104726
doi:

Banques de données

ClinicalTrials.gov
['NCT05483725']

Types de publication

Journal Article

Langues

eng

Pagination

e1645

Informations de copyright

Copyright © 2024 The Author(s). Transplantation Direct. Published by Wolters Kluwer Health, Inc.

Auteurs

Vojtech Petr (V)

Department of Nephrology, Institute for Clinical and Experimental Medicine, Prague, Czech Republic.

Ivan Zahradka (I)

Department of Nephrology, Institute for Clinical and Experimental Medicine, Prague, Czech Republic.

Istvan Modos (I)

Information Technology Department, Institute for Clinical and Experimental Medicine, Prague, Czech Republic.

Matej Roder (M)

Immunogenetics Department, Institute for Clinical and Experimental Medicine, Prague, Czech Republic.

Martina Fialova (M)

Department of Clinical and Transplant Immunology, Institute for Clinical and Experimental Medicine, Prague, Czech Republic.

Jana Machkova (J)

Transplant Laboratory, Institute for Clinical and Experimental Medicine, Prague, Czech Republic.

Katerina Kabrtova (K)

Immunogenetics Department, Institute for Clinical and Experimental Medicine, Prague, Czech Republic.

Petra Hruba (P)

Transplant Laboratory, Institute for Clinical and Experimental Medicine, Prague, Czech Republic.

Maria Magicova (M)

Department of Nephrology, Institute for Clinical and Experimental Medicine, Prague, Czech Republic.

Antonij Slavcev (A)

Immunogenetics Department, Institute for Clinical and Experimental Medicine, Prague, Czech Republic.

Ilja Striz (I)

Department of Clinical and Transplant Immunology, Institute for Clinical and Experimental Medicine, Prague, Czech Republic.

Ondrej Viklicky (O)

Department of Nephrology, Institute for Clinical and Experimental Medicine, Prague, Czech Republic.
Transplant Laboratory, Institute for Clinical and Experimental Medicine, Prague, Czech Republic.

Classifications MeSH