Combination induction therapy with monoclonal antibodies specific for CD80, CD86, and CD154 in nonhuman primate renal transplantation

被引:48
作者
Montgomery, SP
Xu, H
Tadaki, DK
Celniker, A
Burkly, LC
Berning, JD
Cruzata, F
Elster, EA
Gray, G
Kampen, RL
Swanson, SJ
Harlan, DM
Kirk, AD
机构
[1] NIDDK, Transplantat & Autoimmun Branch, Bethesda, MD 20889 USA
[2] Walter Reed Army Med Ctr, Dept Surg, Washington, DC 20307 USA
[3] Wyeth, Andover, MA USA
[4] Biogen Inc, Cambridge, MA USA
关键词
D O I
10.1097/00007890-200211270-00002
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. Antibodies and fusion proteins specific for CD80, CD86, and CD154 have shown promise as agents capable of inducing donor-specific tolerance in rodents. These agents have also been shown to be synergistic with one another in many settings of counter-adaptive immunity. In the nonhuman primate, monoclonal antibodies specific for CD80 and CD86 have prolonged the time to rejection of renal allografts but have not resulted in tolerance. A monoclonal antibody specific for CD154 has resulted in markedly prolonged survival of kidney, islet, cardiac, and skin allografts, but again most animals have eventually developed rejection after prolonged periods of rejection-free survival off therapy. Methods. A combination of monoclonal antibodies specific for CD80, CD86, and CD154 were used in a mismatched nonhuman primate renal-allograft model. Doses used were based on optimized treatment protocols for each agent individually. Results. Treatment of four rhesus macaques with this combination yielded a mean rejection-free survival of 565 days (311-911 days), significantly greater than untreated controls (mean survival = 7.0 days, P = 0.001) and animals treated with only a combination of anti-CD80 and CD86 (mean survival = 191 days, P = 0.01). The survival of animals treated with this combination of monoclonal antibodies was not significantly greater than those treated with anti-CD154 alone, but the production of alloantibody was delayed compared with monotherapy anti-CD154.
引用
收藏
页码:1365 / 1369
页数:5
相关论文
共 18 条
[1]   The role of cytokines, CTLA-4 and costimulation in transplant tolerance and rejection [J].
Dai, ZH ;
Lakkis, FG .
CURRENT OPINION IN IMMUNOLOGY, 1999, 11 (05) :504-508
[2]   Treatment with the humanized CD154-specific monoclonal antibody, hu5C8, prevents acute rejection of primary skin allografts in nonhuman primates [J].
Elster, EA ;
Xu, H ;
Tadaki, DK ;
Montgomery, S ;
Burkly, LC ;
Berning, JD ;
Baumgartner, RE ;
Cruzata, F ;
Marx, R ;
Harlan, DM ;
Kirk, AD .
TRANSPLANTATION, 2001, 72 (09) :1473-1478
[3]   Primate skin allotransplantation with anti-CD154 monotherapy [J].
Elster, EA ;
Xu, H ;
Tadaki, DK ;
Burkly, LC ;
Berning, JD ;
Baumgartner, RE ;
Cruzata, F ;
Patterson, NB ;
Harlan, DM ;
Kirk, AD .
TRANSPLANTATION PROCEEDINGS, 2001, 33 (1-2) :675-676
[4]   Treatment of allograft recipients with donor-specific transfusion and anti-CD154 antibody leads to deletion of alloreactive CD8+ T cells and prolonged craft survival in a CTLA4-dependent manner [J].
Iwakoshi, NN ;
Mordes, JP ;
Markees, TG ;
Phillips, NE ;
Rossini, AA ;
Greiner, DL .
JOURNAL OF IMMUNOLOGY, 2000, 164 (01) :512-521
[5]   Long-term survival and function of intrahepatic islet allografts in baboons treated with humanized anti-CD154 [J].
Kenyon, NS ;
Fernandez, LA ;
Lehmann, R ;
Masetti, M ;
Ranuncoli, A ;
Chatzipetrou, M ;
Iaria, G ;
Han, DM ;
Wagner, JL ;
Ruiz, P ;
Berho, M ;
Inverardi, L ;
Alejandro, R ;
Mintz, DH ;
Kirk, AD ;
Harlan, DM ;
Burkly, LC ;
Ricordi, C .
DIABETES, 1999, 48 (07) :1473-1481
[6]   Long-term survival and function of intrahepatic islet allografts in rhesus monkeys treated with humanized anti-CD154 [J].
Kenyon, NS ;
Chatzipetrou, M ;
Masetti, M ;
Ranuncoli, A ;
Oliveira, M ;
Wagner, JL ;
Kirk, AD ;
Harlan, DM ;
Burkly, LC ;
Ricordi, C .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (14) :8132-8137
[7]   CTLA4-Ig and anti-CD4O ligand prevent renal allograft rejection in primates [J].
Kirk, AD ;
Harlan, DM ;
Armstrong, NN ;
Davis, TA ;
Dong, YC ;
Gray, GS ;
Hong, XN ;
Thomas, D ;
Fechner, JH ;
Knechtle, SJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (16) :8789-8794
[8]   The role of CD154 in organ transplant rejection and acceptance [J].
Kirk, AD ;
Blair, PJ ;
Tadaki, DK ;
Xu, H ;
Harlan, DM .
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 2001, 356 (1409) :691-702
[9]   Induction therapy with monoclonal antibodies specific for CD80 and CD86 delays the onset of acute renal allograft rejection in non-human primates [J].
Kirk, AD ;
Tadaki, DK ;
Celniker, A ;
Batty, DS ;
Berning, JD ;
Colonna, JO ;
Cruzata, F ;
Elster, EA ;
Gray, GS ;
Kampen, RL ;
Patterson, NB ;
Szklut, P ;
Swanson, J ;
Xu, H ;
Harlan, DM .
TRANSPLANTATION, 2001, 72 (03) :377-384
[10]   Treatment with humanized monoclonal antibody against CD154 prevents acute renal allograft rejection in nonhuman primates [J].
Kirk, AD ;
Burkly, LC ;
Batty, DS ;
Baumgartner, RE ;
Berning, JD ;
Buchanan, K ;
Fechner, JH ;
Germond, RL ;
Kampen, RL ;
Patterson, NB ;
Swanson, SJ ;
Tadaki, DK ;
TenHoor, CN ;
White, L ;
Knechtle, SJ ;
Harlan, DM .
NATURE MEDICINE, 1999, 5 (06) :686-693