IPH-2101是一种全人源抗nk细胞抑制受体单克隆抗体,具有治疗血液病的潜力。

Evren Alici
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摘要

nk细胞对肿瘤细胞的活性受抑制和激活信号的复杂平衡调节,这些信号是通过nk细胞受体与肿瘤细胞上表达的激活和抑制配体结合介导的。因此,抑制级联的破坏将使平衡转向激活。先天制药公司(Innate Pharma)正在开发的ip -2101 (1-7F9)是一种全人源IgG4抗杀伤免疫球蛋白样受体(KIR)单抗,用于治疗血液系统恶性肿瘤,如急性髓性白血病(AML)和多发性骨髓瘤(MM)。在临床前研究中,ip -2101选择性结合KIR2DL1、KIR2DL1、KIR2DS1和KIR2DS1、KIR2DS1和kir2ds2,将转染了ir的靶细胞系暴露于ip -2101会导致nk细胞介导的裂解增强。在用ip -2101治疗AML和MM患者的I期临床试验中,观察到NK细胞的活化,并且ip -2101表现出良好的安全性。在本文发表时,MM患者已被招募参加II期临床试验,以评估单药ip -2101或ip -2101联合来那度胺。这些和更大的随机试验是有必要的,以澄清是否通过ip -2101增强患者的nk细胞活性将是治疗血液系统恶性肿瘤的可行方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
IPH-2101, a fully human anti-NK-cell inhibitory receptor mAb for the potential treatment of hematological cancers.

NK-cell activity against tumor cells is regulated by a complex balance of inhibitory and activating signals, which are mediated by the binding of NK-cell receptors to activating and inhibitory ligands expressed on tumor cells. Thus, the disruption of the inhibitory cascade would shift the balance to activation. IPH-2101 (1-7F9), being developed by Innate Pharma, is a fully human IgG4 anti-killer immunoglobulin-like receptor (KIR) mAb for the treatment of hematological malignancies, such as acute myeloid leukemia (AML) and multiple myeloma (MM). In preclinical studies, IPH-2101 selectively bound to KIR2DL1, 2 and 3, and KIR2DS1 and 2, and exposure of KIR-transfected target cell lines to IPH-2101 led to an augmented NK-cell-mediated lysis. In phase I clinical trials in patients with AML and MM treated with IPH-2101, activation of NK cells was observed and IPH-2101 exhibited a good safety profile. At the time of publication, patients with MM had been recruited to phase II clinical trials to assess single-agent IPH-2101 or IPH-2101 in combination with lenalidomide. These and larger, randomized trials are warranted to clarify whether enhancing a patient's NK-cell activity by IPH-2101 will be a viable approach in the treatment of hematological malignancies.

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Current Opinion in Molecular Therapeutics
Current Opinion in Molecular Therapeutics 医学-生物工程与应用微生物
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