共 38 条
The JAK3 inhibitor CP-690550 selectively reduces NK and CD8+cell numbers in cynomolgus monkey blood following chronic oral dosing
被引:60
作者:

Conklyn, M
论文数: 0 引用数: 0
h-index: 0
机构:
Pfizer Inc, Global Res & Dev, Dept Antibacterials Immunol & Canc, Groton, CT 06340 USA Pfizer Inc, Global Res & Dev, Dept Antibacterials Immunol & Canc, Groton, CT 06340 USA

Andresen, C
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h-index: 0
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Pfizer Inc, Global Res & Dev, Dept Antibacterials Immunol & Canc, Groton, CT 06340 USA Pfizer Inc, Global Res & Dev, Dept Antibacterials Immunol & Canc, Groton, CT 06340 USA

Changelian, P
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h-index: 0
机构:
Pfizer Inc, Global Res & Dev, Dept Antibacterials Immunol & Canc, Groton, CT 06340 USA Pfizer Inc, Global Res & Dev, Dept Antibacterials Immunol & Canc, Groton, CT 06340 USA

Kudlacz, E
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h-index: 0
机构:
Pfizer Inc, Global Res & Dev, Dept Antibacterials Immunol & Canc, Groton, CT 06340 USA Pfizer Inc, Global Res & Dev, Dept Antibacterials Immunol & Canc, Groton, CT 06340 USA
机构:
[1] Pfizer Inc, Global Res & Dev, Dept Antibacterials Immunol & Canc, Groton, CT 06340 USA
关键词:
memory T cells;
IL-15;
CD69;
transplantation;
D O I:
10.1189/jlb.0504282
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
Janus kinase 3 (JAK3) is a cytoplasmic tyrosine kinase associated with the common gamma chain, an integral component of cytokine receptors of the interleukin (IL)-2 family, including IL-4, -7, -9, -15, and -21. CP-690550 is a JAK3 inhibitor with immunosuppressive properties under development for transplantation. We evaluated alterations in circulating lymphocyte subsets in cynomolgus monkey blood following chronic (3-week), oral CP-690550 administration. Natural killer (NK) and CD8+ T cell numbers were reduced in a dose- and time-dependent manner; the latter was a primary effect on memory subsets. CD4+ T and B cell numbers were unaffected or slightly increased, respectively. NK cell numbers were reduced similar to80% (vs. 35% in vehicle-treated animals) and returned to baseline levels within 3 weeks following treatment cessation. CD8+ T cells declined by a maximum 43% (vs. 25% for vehicle-treated animals) but rebounded significantly (300%) within 2 weeks after the last dose. Although CP-690550 did not result in reduction of CD4+ T cell number, these cells also increased (225%) within 2 weeks of treatment cessation. IL-15 is important for maintaining homeostasis of these cell types, and CP-690550 inhibited IL-15-induced CD69 expression in NK cells [inhibitory concentration 50% (IC50)=48.0+/-8.4 nM] and CD8+ T cells (IC50 =16.2+/-1.5 nM).
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页码:1248 / 1255
页数:8
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