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HE3286:一种用于自身免疫性疾病口服治疗的新型合成类固醇。

HE3286: a novel synthetic steroid as an oral treatment for autoimmune disease.

作者信息

Ahlem C, Auci D, Mangano K, Reading C, Frincke J, Stickney D, Nicoletti F

机构信息

Hollis-Eden Pharmaceuticals, San Diego, California 92121, USA.

出版信息

Ann N Y Acad Sci. 2009 Sep;1173:781-90. doi: 10.1111/j.1749-6632.2009.04798.x.

Abstract

HE3286 (17alpha-ethynyl-5-androstene-3beta, 7beta, 17beta-triol) is a synthetic derivative of a natural anti-inflammatory steroid, beta-AET (5-androstene-3beta, 7beta, 17beta-triol). HE3286 is orally bioavailable and treats established disease in models of ulcerative colitis, collagen-induced arthritis, and collagen antibody-induced arthritis, reducing clinical signs of disease and proinflammatory signals, including IL-6 and matrix metallopeptidase 3. HE3286 modulates nuclear factor kappaB through an unknown mechanism but does not interact with any of the steroid-binding nuclear hormone receptors and is not immune suppressive. HE3286 was safe and well tolerated in phase I studies and is under evaluation in multicenter phase I/II clinical trials for ulcerative colitis and arthritis. HE3286 may provide a new treatment option for patients with inflammatory and autoimmune diseases.

摘要

HE3286(17α-乙炔基-5-雄烯-3β,7β,17β-三醇)是一种天然抗炎甾体β-AET(5-雄烯-3β,7β,17β-三醇)的合成衍生物。HE3286口服具有生物利用度,可治疗溃疡性结肠炎、胶原诱导性关节炎和胶原抗体诱导性关节炎模型中的已确诊疾病,减轻疾病的临床症状和促炎信号,包括白细胞介素-6和基质金属肽酶3。HE3286通过未知机制调节核因子κB,但不与任何甾体结合核激素受体相互作用,也不具有免疫抑制作用。HE3286在I期研究中安全且耐受性良好,正在针对溃疡性结肠炎和关节炎进行多中心I/II期临床试验评估。HE3286可能为炎症和自身免疫性疾病患者提供一种新的治疗选择。

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