COVID-19 boosters restore virus-specific immune responses in kidney transplant recipients unresponsive to primary vaccination

Kidney transplant recipients (KTRs) often exhibit impaired immune responses to vaccination, necessitating multiple doses to obtain sufficient protection from severe disease. This study compared immunological mechanisms underlying the vaccine-induced response between KTRs who responded to primary vaccination (primary responders) and those who only responded to a booster vaccination (booster responders). Humoral immune responses, including binding and Fc-mediated functionalities, and T cell responses, were generally comparable in primary and booster responders. More in-depth analyses revealed that booster responders had an expanded memory B cell pool and stronger omicron BA.1 neutralization, while primary responders had more IL-21-producing T cells and a distinct SARS-CoV-2-specific CD4 T cell phenotype. Principal component analysis demonstrated that booster responders exhibited a more refined immune network integration. These results suggest that the delayed immune response of booster responders is not functionally impaired and that repeated vaccination is an effective strategy to achieve adequate protection in this population.

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Publication Details

Journal
npj Viruses
Published
2026-02-27
DOI
https://doi.org/10.1038/s44298-026-00178-5
Primary Topic
SARS-CoV-2 and COVID-19 Research
Type
article
Field-Weighted Citation Impact
0.00

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article

COVID-19 boosters restore virus-specific immune responses in kidney transplant recipients unresponsive to primary vaccination

Esther E.B.M Remmerswaal, Yannick van Sleen, Carla C. Baan, Daryl Geers et al.
npj Viruses
SARS-CoV-2 and COVID-19 Research
article

COVID-19 boosters restore virus-specific immune responses in kidney transplant recipients unresponsive to primary vaccination

Esther E.B.M Remmerswaal, Yannick van Sleen, Carla C. Baan, Daryl Geers, Yvette den Hartog, Luca M. Zaeck, Marcia ML Kho, Frederiek J. Bemelman, Rory D. de Vries, Jan-Stephan F. Sanders, Lennert Gommers, Alfonso Abrahams, Dimitri Diavatopoulos, Luuk H. J. Hilbrands, Jan Stephan F. Sanders, Aiko P. J. de Vries, A. Lianne Messchendorp, Debbie van Baarle, Marlies E. J. Reinders, Renate van der Molen
article en

Abstract

Kidney transplant recipients (KTRs) often exhibit impaired immune responses to vaccination, necessitating multiple doses to obtain sufficient protection from severe disease. This study compared immunological mechanisms underlying the vaccine-induced response between KTRs who responded to primary vaccination (primary responders) and those who only responded to a booster vaccination (booster responders). Humoral immune responses, including binding and Fc-mediated functionalities, and T cell responses, were generally comparable in primary and booster responders. More in-depth analyses revealed that booster responders had an expanded memory B cell pool and stronger omicron BA.1 neutralization, while primary responders had more IL-21-producing T cells and a distinct SARS-CoV-2-specific CD4 T cell phenotype. Principal component analysis demonstrated that booster responders exhibited a more refined immune network integration. These results suggest that the delayed immune response of booster responders is not functionally impaired and that repeated vaccination is an effective strategy to achieve adequate protection in this population.

npj VirusesVol. 4(1)
University Medical Center Groningen (NL), Radboud University Nijmegen (NL), University of Groningen (NL), Leiden University Medical Center (NL), Erasmus MC (NL), Radboud University Medical Center (NL), University Medical Center Utrecht (NL), Maastricht University (NL), National Institute for Public Health and the Environment (NL), Erasmus MC Cancer Institute (NL), Amsterdam University Medical Centers (NL), Erasmus University Rotterdam (NL)
ZonMw
Good health and well-being
Openalex Percentile: Top 41%
SARS-CoV-2 and COVID-19 Research
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