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Genetic basis of psoriasis vulgaris and its pharmacogenetic potential.

机译:寻常型牛皮癣的遗传基础及其药理潜力。

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摘要

Psoriasis vulgaris is one of the most prevalent T cell-mediated inflammatory diseases in humans. It is multifactorial in origin and shows polygenic inheritance. Systemic immunosuppressive therapies play an important role in management of severe disease cases but are associated with variable response and toxicity. Within the last decade there have been significant advances in our understanding of the genetic basis of this complex disease and polymorphic candidate genes have been proposed. Susceptibility gene characterization together with an explosion in knowledge of its primary immune basis will further define disease pathways involved in psoriasis pathogenesis. This holds the promise of rational design of new therapeutic agents and pharmacogenetic testing to predict responders from non-responders and those at risk of toxicity.
机译:寻常型牛皮癣是人类中最普遍的T细胞介导的炎症性疾病之一。它起源多因素,显示多基因遗传。全身免疫抑制疗法在重症病例的治疗中起着重要作用,但与可变应答和毒性相关。在过去的十年中,我们对这种复杂疾病的遗传基础的理解有了重大进展,并且已经提出了多态性候选基因。易感性基因表征以及其主要免疫基础知识的突飞猛进将进一步确定与牛皮癣发病机制有关的疾病途径。这为合理设计新的治疗药物和药物遗传学测试提供了希望,从而可以预测无反应者和有毒性风险的反应者。

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