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优化了安全性和药代动力学特征的 pH 选择性抗体 SNS-101 对 VISTA 的抑制作用增强了 PD-1 应答。

VISTA checkpoint inhibition by pH-selective antibody SNS-101 with optimized safety and pharmacokinetic profiles enhances PD-1 response.

机构信息

Sensei Biotherapeutics Inc., 1405 Research Blvd, Suite 125, Rockville, MD, 20850, USA.

genOway, Technopark Gerland, 69007, Lyon, France.

出版信息

Nat Commun. 2024 Apr 4;15(1):2917. doi: 10.1038/s41467-024-47256-x.

Abstract

VISTA, an inhibitory myeloid-T-cell checkpoint, holds promise as a target for cancer immunotherapy. However, its effective targeting has been impeded by issues such as rapid clearance and cytokine release syndrome observed with previous VISTA antibodies. Here we demonstrate that SNS-101, a newly developed pH-selective VISTA antibody, addresses these challenges. Structural and biochemical analyses confirmed the pH-selectivity and unique epitope targeted by SNS-101. These properties confer favorable pharmacokinetic and safety profiles on SNS-101. In syngeneic tumor models utilizing human VISTA knock-in mice, SNS-101 shows in vivo efficacy when combined with a PD-1 inhibitor, modulates cytokine and chemokine signaling, and alters the tumor microenvironment. In summary, SNS-101, currently in Phase I clinical trials, emerges as a promising therapeutic biologic for a wide range of patients whose cancer is refractory to current immunotherapy regimens.

摘要

VISTA,一种抑制性髓系-T 细胞检查点,有望成为癌症免疫疗法的一个靶点。然而,其有效靶向已受到先前 VISTA 抗体所观察到的快速清除和细胞因子释放综合征等问题的阻碍。在这里,我们证明了一种新开发的 pH 选择性 VISTA 抗体 SNS-101 解决了这些挑战。结构和生化分析证实了 SNS-101 的 pH 选择性和独特的表位靶向性。这些特性赋予 SNS-101 有利的药代动力学和安全性特征。在利用人 VISTA 敲入小鼠的同种异体肿瘤模型中,SNS-101 与 PD-1 抑制剂联合使用时表现出体内疗效,调节细胞因子和趋化因子信号,并改变肿瘤微环境。总之,目前处于 I 期临床试验阶段的 SNS-101 是一种很有前途的治疗性生物制剂,适用于广泛的对当前免疫治疗方案有抗药性的癌症患者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5f2b/10995192/56e336c90366/41467_2024_47256_Fig1_HTML.jpg

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