肠道共生双歧杆菌来源的细胞外囊泡调节抗pd -1在肺癌中的治疗作用

IF 15.7 1区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES
Ranjan Preet, Md Atiqul Islam, Jiyoung Shim, Ganeshkumar Rajendran, Amrita Mitra, Vikalp Vishwakarma, Caleb Kutz, Sonali Choudhury, Harsh Pathak, Qun Dai, Weijing Sun, Rashna Madan, Cuncong Zhong, Mary A. Markiewicz, Jun Zhang
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引用次数: 0

摘要

肺癌是全球癌症相关死亡的主要原因。尽管抗程序性死亡-1及其配体1 (PD-1/L1)等免疫疗法是晚期非小细胞肺癌(NSCLC)的标准治疗方法,但许多患者并未直接获益。一些研究已经阐明了通过调节肠道微生物群来提高抗肿瘤免疫反应的新策略。然而,关于肠道微生物群如何远程影响肺癌微环境并随后调节免疫治疗反应,仍然存在很大的争议。本研究表明,共生双歧杆菌衍生的细胞外囊泡(bifi . bevs)可以调节抗pd -1治疗在非小细胞肺癌中的治疗效果。这些Bif。bev主要通过动力蛋白依赖的内吞作用被肺癌细胞吸收,并通过TLR4-NF-κB途径上调PD-L1的表达。它们也能有效地穿透小鼠肠道和患者来源的肺癌类器官。口服这些药。bev导致它们在小鼠肿瘤中积累。采用同种小鼠模型,Bif。bev通过调节关键细胞因子、免疫反应和致癌途径协同抗pd -1的抗肿瘤作用,并增加肿瘤浸润性CD8+ T细胞。因此,我们的研究确定了Bif和Bif之间的联系。bev和肿瘤微环境,提供了另一种机制来解释肠道微生物群如何影响免疫治疗反应,特别是在解剖上远离肠道的肿瘤中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Gut commensal Bifidobacterium-derived extracellular vesicles modulate the therapeutic effects of anti-PD-1 in lung cancer

Gut commensal Bifidobacterium-derived extracellular vesicles modulate the therapeutic effects of anti-PD-1 in lung cancer

Lung cancer is the leading cause of cancer-related deaths worldwide. Although immunotherapy such as anti-programmed death-1 and its ligand 1 (PD-1/L1) is a standard treatment for advanced non-small cell lung cancer (NSCLC), many patients do not derive benefit directly. Several studies have elucidated new strategies to improve the antitumor immune response through gut microbiota modulation. However, it remains largely debatable regarding how gut microbiota remotely affect lung cancer microenvironment and subsequently modulate immunotherapy response. Here we show that commensal Bifidobacterium-derived extracellular vesicles (Bif.BEVs) can modulate the therapeutic effect of anti-PD-1 therapy in NSCLC. These Bif.BEVs are up-taken by lung cancer cells predominantly via dynamin-dependent endocytosis and upregulate PD-L1 expression through TLR4-NF-κB pathway. They also efficiently penetrate murine intestinal and patient-derived lung cancer organoids. Oral gavage of these Bif.BEVs result in their accumulation in tumors in mice. Using a syngeneic mouse model, Bif.BEVs are found to synergize the anti-tumor effect of anti-PD-1 via modulation of key cytokines, immune response and oncogenic pathways, and increase in tumor-infiltrating CD8+ T cells. Our study therefore identifies a link between Bif.BEVs and the tumor microenvironment, providing an alternative mechanism to explain how gut microbiota can influence immunotherapy response, particularly in tumors located anatomically distant from the gut.

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来源期刊
Nature Communications
Nature Communications Biological Science Disciplines-
CiteScore
24.90
自引率
2.40%
发文量
6928
审稿时长
3.7 months
期刊介绍: Nature Communications, an open-access journal, publishes high-quality research spanning all areas of the natural sciences. Papers featured in the journal showcase significant advances relevant to specialists in each respective field. With a 2-year impact factor of 16.6 (2022) and a median time of 8 days from submission to the first editorial decision, Nature Communications is committed to rapid dissemination of research findings. As a multidisciplinary journal, it welcomes contributions from biological, health, physical, chemical, Earth, social, mathematical, applied, and engineering sciences, aiming to highlight important breakthroughs within each domain.
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