Influence of ABCB1 genetic polymorphisms on cyclosporine intracellular concentration in transplant recipients

被引:87
作者
Crettol, Severine [1 ]
Venetz, Jean-Pierre [2 ,3 ]
Fontana, Massimiliano [2 ,3 ]
Aubert, John-David [2 ,3 ]
Ansermot, Nicolas [4 ]
Fathi, Marc [4 ]
Pascual, Manuel [2 ,3 ]
Eap, Chin B. [1 ]
机构
[1] Univ Lausanne, Hop Cer, Dept Psychiat,Unit Biochem & Clin Psychopharmacol, Ctr Psychiat Neurosci,CHUV, CH-1008 Prilly, Switzerland
[2] Univ Lausanne, Geneva, Switzerland
[3] Transplantat Ctr, CHUV, Geneva, Switzerland
[4] Univ Hosp Geneva, Lab Med Serv, Geneva, Switzerland
关键词
ABCB1; cyclosporine; genetic polymorphism; P-glycoprotein; therapeutic drug monitoring;
D O I
10.1097/FPC.0b013e3282f7046f
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Objective The expression on lymphocytes of P-glycoprotein, an efflux transporter encoded by the ABCB1 gene, might influence cyclosporine intracellular concentration. Methods ABCB1 genotypes, cyclosporine intracellular and blood concentrations were determined in 64 stable renal, liver or lung transplant recipients. Results Cyclosporine intracellular concentration correlated moderately with blood concentration (r(2) =0.30, P < 0.00005). The ABCB1 1199A carriers presented a 1.8-fold decreased cyclosporine intracellular concentration (P=0.04), whereas the 3435Tcarriers presented a 1.7-fold increase (P = 0.02) as well as a 1.2-fold increased blood concentration (P=0.04). In contrast, ABCB1 61A > G, 1236C > Tand 2677G > Tpolymorphisms did not influence cyclosporine intracellular and blood concentrations. Conclusion This is the first report demonstrating that ABCB1 polymorphisms influence cyclosporine intracellular concentration. Interestingly, its influence on intracellular concentration is significantly higher than on blood concentration (P < 0.002). This may therefore modulate cyclosporine immunosuppressive activity. Pharmacogenetics and Genomics 18:307-315 (c) 2008 Wolters Kluwer Health vertical bar Lippincott Williams & Wilkins.
引用
收藏
页码:307 / 315
页数:9
相关论文
共 38 条
[11]   A novel MDR1 G1199T variant alters drug resistance and efflux transport activity of P-glycoprotein in recombinant HEK cells [J].
Crouthamel, Matthew H. ;
Wu, Daniel ;
Yang, Ziping ;
Ho, Rodney J. Y. .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2006, 95 (12) :2767-2777
[12]  
DRACH D, 1992, BLOOD, V80, P2729
[13]   MDR1 gene polymorphisms and disposition of the P-glycoprotein substrate fexofenadine [J].
Drescher, S ;
Schaeffeler, E ;
Hitzl, M ;
Hofmann, U ;
Schwab, M ;
Brinkmann, U ;
Eichelbaum, M ;
Fromm, MF .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 2002, 53 (05) :526-534
[14]   CYP3A activity measured by the midazolam test is not related to 3435 C&gt;T polymorphism in the multiple drug resistance transporter gene [J].
Eap, CB ;
Fellay, J ;
Buclin, T ;
Bleiber, G ;
Golay, KP ;
Brocard, M ;
Baumann, P ;
Telenti, A .
PHARMACOGENETICS, 2004, 14 (04) :255-260
[15]   Cyclosporin a has low potency as a calcineurin inhibitor in cells expressing high levels of P-glycoprotein [J].
Fakata, KL ;
Elmquist, WF ;
Swanson, SA ;
Vorce, RL ;
Prince, C ;
Stemmer, PM .
LIFE SCIENCES, 1998, 62 (26) :2441-2448
[16]   P-glycoprotein-170 inhibition significantly reduces cortisol and ciclosporin efflux from human intestinal epithelial cells and T lymphocytes [J].
Farrell, RJ ;
Menconi, MJ ;
Keates, AC ;
Kelly, CP .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2002, 16 (05) :1021-1031
[17]   Response to antiretroviral treatment in HIV-1-infected individuals with allelic variants of the multidrug resistance transporter 1: a pharmacogenetics study [J].
Fellay, J ;
Marzolini, C ;
Meaden, ER ;
Back, DJ ;
Buclin, T ;
Chave, JP ;
Decosterd, LA ;
Furrer, H ;
Opravil, M ;
Pantaleo, G ;
Retelska, D ;
Ruiz, L ;
Schinkel, AH ;
Vernazza, P ;
Eap, CB ;
Telenti, A .
LANCET, 2002, 359 (9300) :30-36
[18]   MDR1 GENE-EXPRESSION IN LYMPHOCYTES OF PATIENTS WITH RENAL-TRANSPLANTS [J].
GOTZL, M ;
WALLNER, J ;
GSUR, A ;
ZOCHBAUER, S ;
KOVARIK, J ;
BALCKE, P ;
PIRKER, R .
NEPHRON, 1995, 69 (03) :277-280
[19]   The C3435T mutation in the human MDR1 gene is associated with altered efflux of the P-glycoprotein substrate rhodamine 123 from CD56+ natural killer cells [J].
Hitzl, M ;
Drescher, S ;
van der Kuip, H ;
Schäffeler, E ;
Fischer, J ;
Schwab, M ;
Eichelbaum, M ;
Fromm, MF .
PHARMACOGENETICS, 2001, 11 (04) :293-298
[20]   Functional polymorphisms of the human multidrug-resistance gene:: Multiple sequence variations and correlation of one allele with P-glycoprotein expression and activity in vivo [J].
Hoffmeyer, S ;
Burk, O ;
von Richter, O ;
Arnold, HP ;
Brockmöller, J ;
Johne, A ;
Cascorbi, I ;
Gerloff, T ;
Roots, I ;
Eichelbaum, M ;
Brinkmann, U .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (07) :3473-3478