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Cellular immunity against cytomegalovirus and risk of infection after kidney transplantation.
Blom, Kjersti B; Kro, Grete B; Midtvedt, Karsten; Jenssen, Trond G; Reisæter, Anna Varberg; Rollag, Hallvor; Hartmann, Anders; Sagedal, Solbjørg; Sjaastad, Ivar; Tylden, Garth; Njølstad, Gro; Nilsen, Einar; Birkeland, Jon A; Åsberg, Anders.
Afiliação
  • Blom KB; Department of Nephrology, Oslo University Hospital, Ullevål, Norway.
  • Kro GB; Institute for Experimental Medical Research, Oslo University Hospital, Ullevål, Norway.
  • Midtvedt K; KG Jebsen Center for Cardiac Research, University of Oslo, Oslo, Norway.
  • Jenssen TG; Faculty of Medicine, University of Oslo, Oslo, Norway.
  • Reisæter AV; Department of Microbiology, Oslo University Hospital, Oslo, Norway.
  • Rollag H; Department of Transplantation Medicine, Oslo University Hospital, Oslo, Norway.
  • Hartmann A; Faculty of Medicine, University of Oslo, Oslo, Norway.
  • Sagedal S; Department of Transplantation Medicine, Oslo University Hospital, Oslo, Norway.
  • Sjaastad I; Department of Transplantation Medicine, Oslo University Hospital, Oslo, Norway.
  • Tylden G; Faculty of Medicine, University of Oslo, Oslo, Norway.
  • Njølstad G; Department of Transplantation Medicine, Oslo University Hospital, Oslo, Norway.
  • Nilsen E; Department of Nephrology, Oslo University Hospital, Ullevål, Norway.
  • Birkeland JA; Institute for Experimental Medical Research, Oslo University Hospital, Ullevål, Norway.
  • Åsberg A; KG Jebsen Center for Cardiac Research, University of Oslo, Oslo, Norway.
Front Immunol ; 15: 1414830, 2024.
Article em En | MEDLINE | ID: mdl-39007131
ABSTRACT

Introduction:

Cytomegalovirus (CMV) infection remains a challenge following kidney transplantation (KTx). Currently, CMV-IgG serostatus at transplantation is used to individualize CMV preventive strategies. We assessed the clinical utility of CMV-IGRA for predicting CMV infection following KTx.

Methods:

We performed a nationwide prospective cohort study from August 2016 until December 2022. Data from all adult KTx recipients in Norway, n=1,546 (R+; n=1,157, D+/R-; n=260, D-/R-; 129), were included with a total of 3,556 CMV-IGRA analyses (1,375 at KTx, 1,188 at eight weeks, 993 one-year after KTx) and 35,782 CMV DNAemia analyses.

Results:

In R+ recipients CMV-IGRA status, measured at any of the time-points, could not identify any differential risk of later CMV infection. D+/R- recipients remaining CMV-IGRA negative 1-year after transplantation (regardless of positive CMV DNAemia and/or CMV IgG status at that time) had increased risk of developing later CMV infection compared to D+/R- recipients who had become CMV-IGRA positive (14% vs. 2%, p=0.01).

Conclusion:

Knowledge of pre-transplant CMV-IGRA status did not provide additional information to CMV-IgG serostatus that could improve current post-transplant CMV treatment algorithms. However, D+/R- recipients with a persisting negative CMV-IGRA one-year after transplantation remained at increased risk of experiencing later CMV infection. Therefore we advocate post-transplant CMV-IGRA monitoring in these patients.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transplante de Rim / Infecções por Citomegalovirus / Citomegalovirus / Imunidade Celular Limite: Adult / Aged / Female / Humans / Male / Middle aged País/Região como assunto: Europa Idioma: En Revista: Front Immunol Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transplante de Rim / Infecções por Citomegalovirus / Citomegalovirus / Imunidade Celular Limite: Adult / Aged / Female / Humans / Male / Middle aged País/Região como assunto: Europa Idioma: En Revista: Front Immunol Ano de publicação: 2024 Tipo de documento: Article