Laboratory for Biomaterial and ImmunoEngineering, Institute of Functional Nano and Soft Materials (FUNSOM), Soochow University, Suzhou, China.
Medical College of Soochow University, Suzhou, China.
Nat Nanotechnol. 2024 Oct;19(10):1569-1578. doi: 10.1038/s41565-024-01722-1. Epub 2024 Jul 25.
Gamma-delta (γδ) T cell-based cancer immunotherapies represent a promising avenue for cancer treatment. However, their development is challenged by the limited expansion and differentiation of the cells ex vivo. Here we induced the endogenous expansion and activation of γδ T cells through oral administration of garlic-derived nanoparticles (GNPs). We found that GNPs could significantly promote the proliferation and activation of endogenous γδ T cells in the intestine, leading to generation of large amount of interferon-γ (IFNγ). Moreover GNP-treated mice showed increased levels of chemokine CXCR3 in intestinal γδ T cells, which can drive their migration from the gut to the tumour environment. The translocation of γδ T cells and IFNγ from the intestine to extraintestinal subcutaneous tumours remodels the tumour immune microenvironment and synergizes with anti-PD-L1, inducing robust antitumour immunity. Our study delineates mechanistic insight into the complex gut-tumour interactome and provides an alternative approach for γδ T cell-based immunotherapy.
基于 γδ(伽马-德尔塔)T 细胞的癌症免疫疗法是癌症治疗的一个很有前途的途径。然而,它们的发展受到细胞体外有限扩增和分化的限制。在这里,我们通过口服大蒜衍生的纳米颗粒(GNPs)诱导内源性 γδ T 细胞的扩增和激活。我们发现 GNPs 可以显著促进肠道内源性 γδ T 细胞的增殖和激活,导致大量干扰素-γ(IFNγ)的产生。此外,经 GNP 处理的小鼠肠道 γδ T 细胞中趋化因子 CXCR3 的水平增加,这可以驱动它们从肠道迁移到肿瘤环境。γδ T 细胞和 IFNγ 从肠道向肠外皮下肿瘤的转移重塑了肿瘤免疫微环境,并与抗 PD-L1 协同作用,诱导强烈的抗肿瘤免疫。我们的研究描绘了肠道-肿瘤相互作用网络的机制见解,并为基于 γδ T 细胞的免疫疗法提供了一种替代方法。