Mycophenolate mofetil inhibits T-cell proliferation in kidney transplant recipients without lowering intracellular dGTP and GTP

被引:12
|
作者
Sankatsing, Sanjay U. C. [1 ,2 ]
Prins, Jan M. [2 ]
Yong, Si-La L. [3 ]
Roelofsen, Jeroen [4 ]
van Kuilenburg, Andre B. P. [4 ]
Kewn, Steve [5 ]
Back, David J. [5 ]
Bemelman, Frederike J. [3 ]
ten Berge, Ineke J. M. [3 ]
机构
[1] Univ Amsterdam, Acad Med Ctr, Div Infect Dis Trop Med & AIDS, Dept Internal Med, NL-1105 AZ Amsterdam, Netherlands
[2] Univ Amsterdam, Ctr Infect & Immun Amsterdam CINIMA, NL-1105 AZ Amsterdam, Netherlands
[3] Univ Amsterdam, Renal Transplant Unit, Acad Med Ctr, NL-1105 AZ Amsterdam, Netherlands
[4] Univ Amsterdam, Dept Genet Metab Dis, Acad Med Ctr, NL-1105 AZ Amsterdam, Netherlands
[5] Univ Liverpool, Dept Pharmacol & Therapeut, Liverpool L69 3BX, Merseyside, England
关键词
dGTP; GTP; mycophenolate mofetil;
D O I
10.1111/j.1432-2277.2008.00739.x
中图分类号
R61 [外科手术学];
学科分类号
摘要
To study if mycophenolic acid (MPA), the active metabolite of mycophenolate mofetil (MMF), indeed inhibits T-cell proliferation in kidney transplant recipients by lowering intracellular deoxyguanosine triphosphate (dGTP) and guanosine triphosphate (GTP) levels. Blood was drawn from 11 kidney transplant recipients. Ex vivo T-cell proliferation was measured by stimulation with phytohemagglutin (PHA) and anti-CD3 monoclonal antibody (mAb). Plasma MPA levels and intracellular dGTP and GTP in peripheral blood mononuclear cells were measured. MMF induces a significant decrease in T-lymphocyte proliferation at all time points (i.e. 24 h, 10 days and 8 weeks) after stimulation with both PHA (P = 0.001, 0.002 and 0.013 respectively) and anti-CD3 mAb (P = 0.004, 0.004 and 0.005 respectively). There was no significant change in intracellular dGTP (P = 0.31, 0.16 and 0.35) or GTP levels (P = 0.99, 0.32 and 0.49) between baseline and day 1, day 10 or week 8. All MPA levels were above the minimal required concentration for the inhibition of lymphocyte proliferation. MMF inhibits T-lymphocyte proliferation in kidney transplant recipients without lowering intracellular dGTP or GTP levels. This suggests another mechanism underlying its immunosuppressive capacity.
引用
收藏
页码:1066 / 1071
页数:6
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