JAK3 inhibition, a viable new modality of immunosuppression for solid organ transplants

被引:61
作者
Borie, DC [1 ]
O'Shea, JJ
Changelian, PS
机构
[1] Stanford Univ, Sch Med, Dept Cardiothorac Surg, Transplantat Immunol Lab, Stanford, CA 94305 USA
[2] Natl Inst Arthritis Musculoskeletal & Skin Dis, Mol Immunol & Inflammat Branch, NIH, Bethesda, MD 20892 USA
[3] Pfizer Global Res & Dev, Antibacterials Immunol & Canc, Groton, CT 06340 USA
关键词
D O I
10.1016/j.molmed.2004.09.007
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
The field of organ transplantation has had tremendous success because of the availability of immunosuppressive drugs that efficiently prevent acute organ rejection. Numerous and severe side effects are, however, associated with all current immunosuppressive therapies and justify a search for drugs with better efficacy and safety profiles. Janus kinase (JAK) 3, a tyrosine kinase that is crucial for mediating signals from the common gamma-chain of cytokine receptors, is peculiar in that its expression, contrarily to the targets of most current immunosuppressive drugs, is limited to cells that actively participate to the immune response to allografts. The recent demonstration in stringent preclinical models that JAK3 inhibition results in efficacy for the prevention of allograft rejection with a narrow side-effect profile might lead to a new era in the field of immunosuppression.
引用
收藏
页码:532 / 541
页数:10
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