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Neutralizing antibody response against the B.1.617.2 (delta) and the B.1.1.529 (omicron) variants after a third mRNA SARS-CoV-2 vaccine dose in kidney transplant recipients.
Benning, Louise; Morath, Christian; Bartenschlager, Marie; Kim, Heeyoung; Reineke, Marvin; Beimler, Jörg; Buylaert, Mirabel; Nusshag, Christian; Kälble, Florian; Reichel, Paula; Töllner, Maximilian; Schaier, Matthias; Klein, Katrin; Benes, Vladimir; Rausch, Tobias; Rieger, Susanne; Stich, Maximilian; Tönshoff, Burkhard; Weidner, Niklas; Schnitzler, Paul; Zeier, Martin; Süsal, Caner; Hien Tran, Thuong; Bartenschlager, Ralf; Speer, Claudius.
  • Benning L; Department of Nephrology, University of Heidelberg, Heidelberg, Germany.
  • Morath C; Department of Nephrology, University of Heidelberg, Heidelberg, Germany.
  • Bartenschlager M; Department of Infectious Diseases, Molecular Virology, University of Heidelberg, Heidelberg, Germany.
  • Kim H; Department of Infectious Diseases, Molecular Virology, University of Heidelberg, Heidelberg, Germany.
  • Reineke M; Department of Nephrology, University of Heidelberg, Heidelberg, Germany.
  • Beimler J; Department of Nephrology, University of Heidelberg, Heidelberg, Germany.
  • Buylaert M; Department of Nephrology, University of Heidelberg, Heidelberg, Germany.
  • Nusshag C; Department of Nephrology, University of Heidelberg, Heidelberg, Germany.
  • Kälble F; Department of Nephrology, University of Heidelberg, Heidelberg, Germany.
  • Reichel P; Department of Nephrology, University of Heidelberg, Heidelberg, Germany.
  • Töllner M; Department of Nephrology, University of Heidelberg, Heidelberg, Germany.
  • Schaier M; Department of Nephrology, University of Heidelberg, Heidelberg, Germany.
  • Klein K; Department of Nephrology, University of Heidelberg, Heidelberg, Germany.
  • Benes V; Genomics Core Facility, European Molecular Biology Laboratory, Heidelberg, Germany.
  • Rausch T; Genomics Core Facility, European Molecular Biology Laboratory, Heidelberg, Germany.
  • Rieger S; Department of Pediatrics I, University Children's Hospital Heidelberg, Heidelberg, Germany.
  • Stich M; Department of Pediatrics I, University Children's Hospital Heidelberg, Heidelberg, Germany.
  • Tönshoff B; Department of Pediatrics I, University Children's Hospital Heidelberg, Heidelberg, Germany.
  • Weidner N; Department of Virology, University of Heidelberg, Heidelberg, Germany.
  • Schnitzler P; Department of Virology, University of Heidelberg, Heidelberg, Germany.
  • Zeier M; Department of Nephrology, University of Heidelberg, Heidelberg, Germany.
  • Süsal C; Institute of Immunology, University of Heidelberg, Heidelberg, Germany.
  • Hien Tran T; Transplant Immunology Research Center of Excellence, Koç University Hospital, Istanbul, Turkey.
  • Bartenschlager R; Institute of Immunology, University of Heidelberg, Heidelberg, Germany.
  • Speer C; Department of Infectious Diseases, Molecular Virology, University of Heidelberg, Heidelberg, Germany.
Am J Transplant ; 22(7): 1873-1883, 2022 07.
Article en En | MEDLINE | ID: mdl-35384272
ABSTRACT
Seroconversion after COVID-19 vaccination is impaired in kidney transplant recipients. Emerging variants of concern such as the B.1.617.2 (delta) and the B.1.1.529 (omicron) variants pose an increasing threat to these patients. In this observational cohort study, we measured anti-S1 IgG, surrogate neutralizing, and anti-receptor-binding domain antibodies three weeks after a third mRNA vaccine dose in 49 kidney transplant recipients and compared results to 25 age-matched healthy controls. In addition, vaccine-induced neutralization of SARS-CoV-2 wild-type, the B.1.617.2 (delta), and the B.1.1.529 (omicron) variants was assessed using a live-virus assay. After a third vaccine dose, anti-S1 IgG, surrogate neutralizing, and anti-receptor-binding domain antibodies were significantly lower in kidney transplant recipients compared to healthy controls. Only 29/49 (59%) sera of kidney transplant recipients contained neutralizing antibodies against the SARS-CoV-2 wild-type or the B.1.617.2 (delta) variant and neutralization titers were significantly reduced compared to healthy controls (p < 0.001). Vaccine-induced cross-neutralization of the B.1.1.529 (omicron) variants was detectable in 15/35 (43%) kidney transplant recipients with seropositivity for anti-S1 IgG, surrogate neutralizing, and/or anti-RBD antibodies. Neutralization of the B.1.1.529 (omicron) variants was significantly reduced compared to neutralization of SARS-CoV-2 wild-type or the B.1.617.2 (delta) variant for both, kidney transplant recipients and healthy controls (p < .001 for all).
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Trasplante de Riñón / COVID-19 Tipo de estudio: Observational_studies / Prognostic_studies Límite: Humans Idioma: En Año: 2022 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Trasplante de Riñón / COVID-19 Tipo de estudio: Observational_studies / Prognostic_studies Límite: Humans Idioma: En Año: 2022 Tipo del documento: Article