TY - JOUR
T1 - Conventional immunosuppression is compatible with costimulation blockade-based, mixed chimerism tolerance induction
AU - Adams, Andrew B.
AU - Shirasugi, Nozomu
AU - Jones, Thomas R.
AU - Williams, Matthew A.
AU - Durham, Megan M.
AU - Ha, Jongwon
AU - Dong, Ying
AU - Guo, Zhong
AU - Newell, Kenneth A.
AU - Pearson, Thomas C.
AU - Larsen, Christian P.
PY - 2003/7
Y1 - 2003/7
N2 - T-cell costimulatory blockade has emerged as an effective strategy to prevent allograft rejection in experimental models. We and others have reported that the beneficial effects of costimulation blockade can be negated when combined with certain immunosuppressants. The current study evaluates the compatibility of various immunosuppressive agents in a costimulation blockade-based, mixed chimerism tolerance protocol. The addition of conventional agents, including calcineurin inhibitors, did not interfere with tolerance induction. All mice developed multilineage macrochimerism and accepted donor allografts. Analysis of specific T-cell receptor utilization demonstrated selective deletion of donor-reactive T cells. Challenge with donor and third-party allografts confirmed donor-specific tolerance. Clinical introduction of costimulation blockade-based strategies will likely incorporate currently approved immunosuppressive agents. While it has been reported that certain conventional agents are detrimental to costimulation blockade-based strategies, our results suggest that these agents could safely be combined in clinical trials when used as part of a nonmyelosuppressive, mixed chimerism-based tolerance strategy.
AB - T-cell costimulatory blockade has emerged as an effective strategy to prevent allograft rejection in experimental models. We and others have reported that the beneficial effects of costimulation blockade can be negated when combined with certain immunosuppressants. The current study evaluates the compatibility of various immunosuppressive agents in a costimulation blockade-based, mixed chimerism tolerance protocol. The addition of conventional agents, including calcineurin inhibitors, did not interfere with tolerance induction. All mice developed multilineage macrochimerism and accepted donor allografts. Analysis of specific T-cell receptor utilization demonstrated selective deletion of donor-reactive T cells. Challenge with donor and third-party allografts confirmed donor-specific tolerance. Clinical introduction of costimulation blockade-based strategies will likely incorporate currently approved immunosuppressive agents. While it has been reported that certain conventional agents are detrimental to costimulation blockade-based strategies, our results suggest that these agents could safely be combined in clinical trials when used as part of a nonmyelosuppressive, mixed chimerism-based tolerance strategy.
KW - Costimulatory molecules
KW - Immunosuppressive drugs
KW - Mixed chimerism
KW - Transplantation tolerance
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U2 - 10.1034/j.1600-6143.2003.00155.x
DO - 10.1034/j.1600-6143.2003.00155.x
M3 - Article
C2 - 12814483
AN - SCOPUS:10744232531
SN - 1600-6135
VL - 3
SP - 895
EP - 901
JO - American Journal of Transplantation
JF - American Journal of Transplantation
IS - 7
ER -