Janus kinase 3 inhibition with CP‐690,550 prevents allograft vasculopathy

Summary Janus kinase 3 (JAK3) mediates signal transduction from cytokine receptors using the common γ chain. The rationally designed inhibitor of JAK3, CP‐690,550, prevents acute allograft rejection in rodents and in nonhuman primates. Here we investigated the ability of CP‐690,550, to prevent allog...

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Veröffentlicht in:Transplant international 2006-12, Vol.19 (12), p.1014-1021
Hauptverfasser: Rousvoal, Geraldine, Si, Ming‐Sing, Lau, Macy, Zhang, Sally, Berry, Gerald J., Flores, Mona G., Changelian, Paul S., Reitz, Bruce A., Borie, Dominic C.
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container_end_page 1021
container_issue 12
container_start_page 1014
container_title Transplant international
container_volume 19
creator Rousvoal, Geraldine
Si, Ming‐Sing
Lau, Macy
Zhang, Sally
Berry, Gerald J.
Flores, Mona G.
Changelian, Paul S.
Reitz, Bruce A.
Borie, Dominic C.
description Summary Janus kinase 3 (JAK3) mediates signal transduction from cytokine receptors using the common γ chain. The rationally designed inhibitor of JAK3, CP‐690,550, prevents acute allograft rejection in rodents and in nonhuman primates. Here we investigated the ability of CP‐690,550, to prevent allograft vasculopathy in a rodent model of aorta transplantation. Aortas from AxC Irish (RT1a) or Lewis (RT1l) rats were heterotopically transplanted into the infra‐renal aorta of Lewis recipients and harvested at 28 or 56 days. Treated recipients received CP‐690,550 by osmotic pumps (mean drug exposure of 110 ± 38 ng/ml). Significant intimal hyperplasia was demonstrated in untreated allografts when compared with isografts at 28 days (2.08 ± 0.85% vs. 0.43 ± 0.2% luminal obliteration, respectively, P = 0.001) and 56 days (5.3 ± 2.4% vs. 0.38 ± 0.3%, P = 0.002). Treatment caused a 51% reduction in intimal hyperplasia at day 56. CP‐690,550‐treated animals also had a significant reduction of donor‐specific IgG production and of the gene expression for suppressor of cytokine signaling‐3 and with unchanged levels of expression of RANTES, IP‐10 and transforming growth factor‐β1. These results are the first to show that JAK3 blockade by CP‐690,550 effectively prevents allograft vasculopathy in this rat model of aorta transplantation.
doi_str_mv 10.1111/j.1432-2277.2006.00387.x
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The rationally designed inhibitor of JAK3, CP‐690,550, prevents acute allograft rejection in rodents and in nonhuman primates. Here we investigated the ability of CP‐690,550, to prevent allograft vasculopathy in a rodent model of aorta transplantation. Aortas from AxC Irish (RT1a) or Lewis (RT1l) rats were heterotopically transplanted into the infra‐renal aorta of Lewis recipients and harvested at 28 or 56 days. Treated recipients received CP‐690,550 by osmotic pumps (mean drug exposure of 110 ± 38 ng/ml). Significant intimal hyperplasia was demonstrated in untreated allografts when compared with isografts at 28 days (2.08 ± 0.85% vs. 0.43 ± 0.2% luminal obliteration, respectively, P = 0.001) and 56 days (5.3 ± 2.4% vs. 0.38 ± 0.3%, P = 0.002). Treatment caused a 51% reduction in intimal hyperplasia at day 56. CP‐690,550‐treated animals also had a significant reduction of donor‐specific IgG production and of the gene expression for suppressor of cytokine signaling‐3 and with unchanged levels of expression of RANTES, IP‐10 and transforming growth factor‐β1. 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The rationally designed inhibitor of JAK3, CP‐690,550, prevents acute allograft rejection in rodents and in nonhuman primates. Here we investigated the ability of CP‐690,550, to prevent allograft vasculopathy in a rodent model of aorta transplantation. Aortas from AxC Irish (RT1a) or Lewis (RT1l) rats were heterotopically transplanted into the infra‐renal aorta of Lewis recipients and harvested at 28 or 56 days. Treated recipients received CP‐690,550 by osmotic pumps (mean drug exposure of 110 ± 38 ng/ml). Significant intimal hyperplasia was demonstrated in untreated allografts when compared with isografts at 28 days (2.08 ± 0.85% vs. 0.43 ± 0.2% luminal obliteration, respectively, P = 0.001) and 56 days (5.3 ± 2.4% vs. 0.38 ± 0.3%, P = 0.002). Treatment caused a 51% reduction in intimal hyperplasia at day 56. CP‐690,550‐treated animals also had a significant reduction of donor‐specific IgG production and of the gene expression for suppressor of cytokine signaling‐3 and with unchanged levels of expression of RANTES, IP‐10 and transforming growth factor‐β1. 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CP‐690,550‐treated animals also had a significant reduction of donor‐specific IgG production and of the gene expression for suppressor of cytokine signaling‐3 and with unchanged levels of expression of RANTES, IP‐10 and transforming growth factor‐β1. These results are the first to show that JAK3 blockade by CP‐690,550 effectively prevents allograft vasculopathy in this rat model of aorta transplantation.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>17081232</pmid><doi>10.1111/j.1432-2277.2006.00387.x</doi><tpages>8</tpages></addata></record>
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subjects Animals
Aorta - transplantation
Arteriosclerosis - prevention & control
Biological and medical sciences
Chemokine CCL5 - genetics
chronic rejection
CP‐690
General aspects
Hyperplasia
Interferon-gamma - biosynthesis
Janus kinase 3
Janus Kinase 3 - antagonists & inhibitors
Killer Cells, Natural - immunology
Male
Medical sciences
Nephrology. Urinary tract diseases
Pharmacology. Drug treatments
Piperidines
Protein Kinase Inhibitors - pharmacology
Pyrimidines - pharmacology
Pyrroles - pharmacology
Rats
Rats, Inbred ACI
Rats, Inbred Lew
Suppressor of Cytokine Signaling 3 Protein
Suppressor of Cytokine Signaling Proteins - genetics
Transplantation, Homologous
Tunica Intima - pathology
title Janus kinase 3 inhibition with CP‐690,550 prevents allograft vasculopathy
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