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一种基于酵母的口服疗法可递送免疫检查点抑制剂以减轻肠道肿瘤负担。

A yeast-based oral therapeutic delivers immune checkpoint inhibitors to reduce intestinal tumor burden.

作者信息

Rebeck Olivia N, Wallace Miranda J, Prusa Jerome, Ning Jie, Evbuomwan Esse M, Rengarajan Sunaina, Habimana-Griffin LeMoyne, Kwak Suryang, Zahrah David, Tung Jason, Liao James, Mahmud Bejan, Fishbein Skye R S, Ramirez Tovar Erick S, Mehta Rehan, Wang Bin, Gorelik Mark G, Helmink Beth A, Dantas Gautam

机构信息

The Edison Family Center for Genome Sciences and Systems Biology, Washington University School of Medicine, St. Louis, MO 63110, USA; Department of Pathology and Immunology, Division of Laboratory and Genomic Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA.

The Edison Family Center for Genome Sciences and Systems Biology, Washington University School of Medicine, St. Louis, MO 63110, USA; Department of Pathology and Immunology, Division of Laboratory and Genomic Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA; Department of Biomedical Engineering, Washington University in St. Louis, St. Louis, MO 63130, USA.

出版信息

Cell Chem Biol. 2025 Jan 16;32(1):98-110.e7. doi: 10.1016/j.chembiol.2024.10.013. Epub 2024 Nov 20.

Abstract

Engineered probiotics are an emerging platform for in situ delivery of therapeutics to the gut. Herein, we developed an orally administered, yeast-based therapeutic delivery system to deliver next-generation immune checkpoint inhibitor (ICI) proteins directly to gastrointestinal tumors. We engineered Saccharomyces cerevisiae var. boulardii (Sb), a probiotic yeast with high genetic tractability and innate anticancer activity, to secrete "miniature" antibody variants that target programmed death ligand 1 (Sb_haPD-1). When tested in an ICI-refractory colorectal cancer (CRC) mouse model, Sb_haPD-1 significantly reduced intestinal tumor burden and resulted in significant shifts to the immune cell profile and microbiome composition. This oral therapeutic platform is modular and highly customizable, opening new avenues of targeted drug delivery that can be applied to treat a myriad of gastrointestinal malignancies.

摘要

工程益生菌是一种新兴的将治疗药物原位递送至肠道的平台。在此,我们开发了一种口服的、基于酵母的治疗性递送系统,以将下一代免疫检查点抑制剂(ICI)蛋白直接递送至胃肠道肿瘤。我们对酿酒酵母变种布拉氏酵母(Sb)进行了工程改造,这是一种具有高遗传易处理性和固有抗癌活性的益生菌酵母,使其分泌靶向程序性死亡配体1的“微型”抗体变体(Sb_haPD-1)。当在ICI难治性结直肠癌(CRC)小鼠模型中进行测试时,Sb_haPD-1显著降低了肠道肿瘤负担,并导致免疫细胞谱和微生物群组成发生显著变化。这种口服治疗平台具有模块化且高度可定制的特点,为靶向药物递送开辟了新途径,可应用于治疗多种胃肠道恶性肿瘤。

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