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SARS-CoV-2 Vaccination in Kidney Transplant Recipients—Stratified Analysis of the Humoral Immune Response

Kidney transplant recipients are at increased risk of SARS-CoV-2 infection and a more severe course of COVID-19. METHODS. We conducted a quantitative serologic testing of antibodies specific for the wild type of SARS-CoV-2 and the Omicron variant of concern before and after a third-dose vaccination,...

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Detalles Bibliográficos
Autores principales: Lammert, Alexander, Schnuelle, Peter, Rabenau, Holger F., Ciesek, Sandra, Krämer, Bernhard K., Göttmann, Uwe, Drüschler, Felix, Keller, Christine, Rose, Daniela, Blume, Carsten, Thomas, Michael, Kohmer, Niko, Lammert, Anne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9575732/
https://www.ncbi.nlm.nih.gov/pubmed/36259077
http://dx.doi.org/10.1097/TXD.0000000000001384
Descripción
Sumario:Kidney transplant recipients are at increased risk of SARS-CoV-2 infection and a more severe course of COVID-19. METHODS. We conducted a quantitative serologic testing of antibodies specific for the wild type of SARS-CoV-2 and the Omicron variant of concern before and after a third-dose vaccination, either mRNA-1273 (Moderna) or BNT162b2 (Pfizer-BioNTech) in a cohort of 103 stable kidney transplant recipients (median [range] age, 58 [22–84] y, 57 men [55.3%]). RESULTS. Third-dose vaccination increased the seroconversion rate from 57.3% to 71.8%. However, despite a marked rise of the antibody concentrations after the booster, 55.4% and 11.6% only formed neutralizing antibodies against the SARS-CoV-2 wild type and Omicron, respectively. Treatment with mycophenolic acid/mycophenolate mofetil (in strata of the dose quartiles), advanced age, and‚ above all‚ impaired renal function (eGFR <60 mL/min) adversely influenced the humoral immunity regarding seroconversion and inhibition of the wild type of SARS-CoV-2. CONCLUSIONS. Apart from immunosuppressive therapy, the humoral vaccination response is largely affected by nonmodifiable factors in kidney transplant recipients. With the currently leading and clinically easier Omicron variant, this puts into perspective the strategy to significantly enhance the protective efficacy of the available vaccines by reducing or temporarily stopping proliferation inhibitors, not least considering the inherent rejection risk with a possible deterioration of graft function.