Combined immunosuppression of mycophenolate mofetil and FK506 for myoblast transplantation in mdx mice

被引:25
作者
Camirand, G [1 ]
Caron, NJ [1 ]
Asselin, I [1 ]
Tremblay, JP [1 ]
机构
[1] Univ Laval, CHU Laval, Unite Rech Genet Humaine, Ctr Rech, Quebec City, PQ G1V 4G2, Canada
关键词
D O I
10.1097/00007890-200107150-00010
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Overcoming adverse effects of immunosuppressors can be achieved by combining different drugs, thus allowing a dosage reduction. Myoblast transplantation is a potential therapy for Duchenne muscular dystrophy, Our research group previously established that FK506 (tacrolimus) is an effective immunosuppressive drug for myoblast transplantation in mice and monkeys. Methods. In the present study, a reduced dose of FK506 at 1.0 mg/kg/day was used in combination with mycophenolate mofetil (MMF; 80 mg/kg/day) as an immunosuppressive protocol for myoblast transplantation. Graft success was evaluated by quantifying the number of dystrophin-positive fibers per muscle section that were injected with normal cells. Results. MMF used alone could not prevent immune rejection of the transplanted myoblasts, MMF given in combination with FK506 immediately after transplantation reduced the success of myoblast transplantation by about 50%. A low dose of FK506 combined with MMF after the establishment of the graft (3 weeks) maintained graft success and controlled immune infiltration compared with a low dose of FK506 alone. However, lymphocyte infiltration was observed at longer term using a low dose of FK506 combined with MMF, Conclusions. The diminution of graft success when combining FK506 and MMF by the time of myoblast transplantation could be attributed to the inhibition of myoblast fusion by MMF, The use of MMF and FK506 after the establishment of the graft did not reduce graft success, however, this combination was not effective at controlling long-term immune rejection in comparison with the optimal dose of FK506 alone.
引用
收藏
页码:38 / 44
页数:7
相关论文
共 51 条
[1]  
Ahsan N, 1997, CLIN TRANSPLANT, V11, P94
[2]   REGENERATION OF SKELETAL-MUSCLE FIBERS FROM AUTOLOGOUS SATELLITE CELLS MULTIPLIED INVITRO - AN EXPERIMENTAL-MODEL FOR TESTING CULTURED-CELL MYOGENICITY [J].
ALAMEDDINE, HS ;
DEHAUPAS, M ;
FARDEAU, M .
MUSCLE & NERVE, 1989, 12 (07) :544-555
[3]  
ALLISON AC, 1994, TRANSPLANT P, V26, P3205
[4]   The nephrotoxicity of new and old immunosuppressive drugs [J].
Bennett, WM .
RENAL FAILURE, 1998, 20 (05) :687-690
[5]   DUCHENNE MUSCULAR-DYSTROPHY - DEFICIENCY OF DYSTROPHIN AT THE MUSCLE-CELL SURFACE [J].
BONILLA, E ;
SAMITT, CE ;
MIRANDA, AF ;
HAYS, AP ;
SALVIATI, G ;
DIMAURO, S ;
KUNKEL, LM ;
HOFFMAN, EP ;
ROWLAND, LP .
CELL, 1988, 54 (04) :447-452
[6]   Molecular mechanisms of action of new xenobiotic immunosuppressive drugs: Tacrolimus (FK506), sirolimus (rapamycin), mycophenolate mofetil and leflunomide [J].
Brazelton, TR ;
Morris, RE .
CURRENT OPINION IN IMMUNOLOGY, 1996, 8 (05) :710-720
[7]   Tacrolimus/mycophenolate provides superior immunosuppression relative to neoral/mycophenolate in synchronous pancreas-kidney transplantation [J].
Bruce, DS ;
Woodle, ES ;
Newell, KA ;
Millis, JM ;
Cronin, DC ;
Loss, GE ;
Grewal, HP ;
Siegel, CT ;
Pellar, S ;
Josephson, MA ;
Thistlethwaite, JR .
TRANSPLANTATION PROCEEDINGS, 1998, 30 (04) :1538-1540
[8]   A CDNA CLONE FROM THE DUCHENNE BECKER MUSCULAR-DYSTROPHY GENE [J].
BURGHES, AHM ;
LOGAN, C ;
HU, XY ;
BELFALL, B ;
WORTON, RG ;
RAY, PN .
NATURE, 1987, 328 (6129) :434-437
[9]   Male-specific competitive PCR for the quantification of transplanted cells in mice [J].
Caron, NJ ;
Chapdelaine, P ;
Tremblay, JP .
BIOTECHNIQUES, 1999, 27 (03) :424-+
[10]   Neural cell adhesion molecule (NCAM) and myoblast fusion [J].
Charlton, CA ;
Mohler, WA ;
Blau, HM .
DEVELOPMENTAL BIOLOGY, 2000, 221 (01) :112-119