Cauli Alberto, Porru Giovanni, Piga Matteo, Vacca Alessandra, Dessole Grazia, Mathieu Alessandro
Rheumatology Unit, Department of Medical Sciences, Policlinico of University of Cagliari, Monserrato, Italy.
Immunotargets Ther. 2014 Jun 9;3:91-6. doi: 10.2147/ITT.S40199. eCollection 2014.
Psoriatic arthritis (PsA) is a frequent chronic inflammatory disease characterized by joint and skin involvement, and by typical extra-articular manifestations. Although the pathogenesis of PsA is still under investigation, the available evidence suggests the importance of the patient's genetic background, microbial or environmental triggers, and an imbalance in the adaptive and acquired immune system, resulting in the production of inflammatory mediators. New therapeutic approaches have been proposed, among them the use of modulators of intracellular signals and gene transcription such as PDE4-inhibiting compounds, which are able to modulate the activity of transcription factors such as CREB and NF-κB and therefore the synthesis of inflammatory mediators, resulting in immunoregulation. This paper summarizes the mechanism of action of apremilast, a PDE4 inhibitor, and the clinical data available on its clinical efficacy and safety profile in the treatment of PsA patients.
银屑病关节炎(PsA)是一种常见的慢性炎症性疾病,其特征为关节和皮肤受累,以及典型的关节外表现。尽管PsA的发病机制仍在研究中,但现有证据表明患者的遗传背景、微生物或环境触发因素以及适应性和后天免疫系统失衡的重要性,这些因素导致炎症介质的产生。已经提出了新的治疗方法,其中包括使用细胞内信号和基因转录调节剂,如磷酸二酯酶4(PDE4)抑制化合物,这些化合物能够调节转录因子如环磷腺苷效应元件结合蛋白(CREB)和核因子κB(NF-κB)的活性,从而调节炎症介质的合成,实现免疫调节。本文总结了PDE4抑制剂阿普斯特的作用机制,以及其治疗PsA患者的临床疗效和安全性方面的现有临床数据。