A Validated LC-MS/MS Method for Performing Belatacept Drug Monitoring in Renal Transplantation

被引:3
|
作者
Chhun, Stephanie [1 ,2 ]
Trauchessec, Mathieu [3 ]
Melicine, Sophie [1 ]
Nicolas, Frederic [4 ]
Miele, Agathe [3 ]
Lukic, Srboljub [1 ]
Vilain, Estelle [4 ]
Amrouche, Lucile [4 ]
Lebert, Dorothee [3 ]
Anglicheau, Dany [2 ,4 ]
Tartour, Eric [1 ,2 ]
Zuber, Julien [2 ,4 ]
机构
[1] Georges Pompidou European Hosp, Necker Hosp, AP HP, Lab Immunol, F-75015 Paris, France
[2] Univ Paris Cite, Fac Med, F-75006 Paris, France
[3] Promise Prote, F-38040 Grenoble, France
[4] Hop Necker Enfants Malad, AP HP, Dept Kidney & Metab Dis, Transplantat & Clin Immunol, F-75015 Paris, France
关键词
belatacept; CTLA4-Ig; transplantation; kidney; pharmacokinetic; RISK;
D O I
10.3390/biomedicines11112955
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Belatacept, a CTLA4-Ig, was designed to prevent rejection and graft loss in kidney transplant recipients. This immunotherapy showed a long-term clinical benefit mainly on renal function and better glycemic control but was also associated with a higher number of severe infectious diseases, particularly CMV disease, and lymphoproliferative disease. Therapeutic drug monitoring usually guides the benefit-risk assessment of long-term immunosuppression. In this study, an analytical method by LC-MS/MS was developed in 20 microL of plasma for the belatacept quantification. Intra- and inter-assay precision and accuracy were lower than 20% for the limit of quantification, and 15% for higher concentrations. The method was implemented in our lab and provided data about the inter-variability (N = 108) and intra-variability (N = 33) of belatacept concentrations in kidney transplant recipients with a stable renal function, after conversion from a CNI- to a belatacept-based regimen.
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页数:11
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