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IPH4102,一种针对免疫受体分子 KIR3DL2 的单克隆抗体,用于治疗皮肤 T 细胞淋巴瘤。

IPH4102, a monoclonal antibody directed against the immune receptor molecule KIR3DL2, for the treatment of cutaneous T-cell lymphoma.

机构信息

a Department of Haematology , Peter MacCallum Cancer Centre , Melbourne , Victoria , Australia.

b Department of Dermatology , Hôpital Saint-Louis , Paris , France.

出版信息

Expert Opin Investig Drugs. 2018 Aug;27(8):691-697. doi: 10.1080/13543784.2018.1498081. Epub 2018 Jul 17.

Abstract

Therapeutic options for mycosis fungoides and Sézary syndrome include a variety of immunomodulatory, epigenetic, and cytotoxic options; however, none has been demonstrated to be efficacious for all patients, or to deliver deep and durable responses to the majority of patients. In this review, we examine the monoclonal antibody, IPH4102, a novel agent for the treatment of cutaneous T-cell lymphoma. Areas covered: In this review, we examine data demonstrating the tissue specificity of KIR3DL2 receptor, which is highly expressed on the malignant cells in cutaneous T-cell lymphoma, including mycosis fungoides and Sézary syndrome. This specificity has led to the development of the agent IPH4102. Preclinical data showing efficacy of IPH4102 in vivo are outlined, as well as the results from Phase I clinical trials, which suggest that the agent is both efficacious and well-tolerated. Larger scale clinical trials are to follow. Expert Opinion: We examine the putative benefit of IPH4102 in comparison to established agents already in the clinic, highlighting its efficacy and relative safety. We also examine possible directions that may better define the role of IPH4102 in the treatment of T-cell lymphoma in the future.

摘要

蕈样肉芽肿和赛泽里综合征的治疗选择包括多种免疫调节、表观遗传和细胞毒性选择;然而,没有一种方法被证明对所有患者都有效,也没有一种方法能对大多数患者产生深度和持久的反应。在这篇综述中,我们研究了用于治疗皮肤 T 细胞淋巴瘤的新型单克隆抗体 IPH4102。

涵盖的领域

在这篇综述中,我们研究了数据表明 KIR3DL2 受体的组织特异性,该受体在皮肤 T 细胞淋巴瘤,包括蕈样肉芽肿和赛泽里综合征中的恶性细胞上高度表达。这种特异性导致了该药物 IPH4102 的开发。概述了体内显示 IPH4102 疗效的临床前数据,以及 I 期临床试验的结果,表明该药物既有效又耐受良好。更大规模的临床试验即将进行。

专家意见

我们将 IPH4102 的潜在益处与已经在临床中使用的现有药物进行了比较,强调了它的疗效和相对安全性。我们还研究了可能的方向,这些方向可能会更好地确定 IPH4102 在未来治疗 T 细胞淋巴瘤中的作用。

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