Expression of killer cell immunoglobulin-like receptors (KIRs) by natural killer cells during acute CMV infection after kidney transplantation.

Détails

ID Serval
serval:BIB_82EEC95F7CB9
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Titre
Expression of killer cell immunoglobulin-like receptors (KIRs) by natural killer cells during acute CMV infection after kidney transplantation.
Périodique
Transplant Immunology
Auteur(s)
de Rham C., Hadaya K., Bandelier C., Ferrari-Lacraz S., Villard J.
ISSN
1878-5492 (Electronic)
ISSN-L
0966-3274
Statut éditorial
Publié
Date de publication
2014
Peer-reviewed
Oui
Volume
31
Numéro
3
Pages
157-164
Langue
anglais
Notes
Publication types: Publication Status: ppublish
Résumé
Human cytomegalovirus (CMV) infection may be a serious complication related to immunosuppression after solid organ transplantation. Due to their cytotoxicity, T-cells and natural killer (NK) cells target and clear the virus from CMV-infected cells. Although immunosuppressive drugs suppress T-cell proliferation and activation, they do not affect NK cells that are crucial for controlling the infection. The regulation of NK cells depends on a wide range of activating and inhibitory receptors such as the family of killer-cell immunoglobulin-like receptors (KIRs). Several human genetic studies have demonstrated the association of KIR genes with the clearance of infections. Since the respective activities of the different KIR proteins expressed by NK cells during CMV infection have not been extensively studied, we analyzed the expression of KIRs in a cohort of 22 CMV-IgG(+) renal transplant patients at the time of CMV reactivation, after antiviral therapy and 6 months later. Our data revealed a marked expression of KIR3DL1 during the acute phase of the reactivation. We set up an in vitro model in which NK cells, derived either from healthy donors or from transplanted patients, target allogeneic fibroblasts, CMV-infected or uninfected. Our results demonstrate a significant correlation between the lysis of CMV-infected fibroblasts and the expression of KIR3DL1. Blocking experiments with antibodies to MHC-I, to NKG2D and to NKG2C confirmed the importance of KIR3DL1. Consequently, our results suggest that KIR proteins and especially KIR3DL1 could play an important role during CMV-infection or CMV reactivation in immunosuppressed patients.
Pubmed
Web of science
Création de la notice
18/12/2014 19:45
Dernière modification de la notice
03/03/2018 18:51
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