RNF43 p.G659fs 通过 PI3K/AKT/mTOR 信号通路和 HLA-E 上调导致 MSI-high 结直肠癌中 NK 细胞功能障碍
RNF43 p.G659fs leads to natural killer cell dysfunction in MSI-high colorectal cancer through PI3K/AKT/mTOR signaling and HLA-E up-regulation.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Engineered Lactococcus lactis secreting Flt3L and OX40 ligand for in situ vaccination-based cancer immunotherapy.
Engineered Lactococcus lactis secreting Flt3L and OX40 ligand for in situ vaccination-based cancer immunotherapy.
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原位疫苗是一种有前景的策略,可将免疫抑制性肿瘤微环境转化为免疫刺激性微环境,且全身暴露和副作用有限。然而,持续的临床获益需要长期且多维度的免疫激活,包括固有免疫和适应性免疫。
在此,我们开发了一种基于益生菌食品级乳酸乳球菌的原位疫苗(FOLactis),其表达Fms样酪氨酸激酶3配体与共刺激分子OX40配体的融合蛋白。瘤内递送FOLactis有助于治疗药物的局部滞留和持续释放,从而全面调节抗肿瘤免疫应答的关键组分,如激活肿瘤及肿瘤引流淋巴结中的NK 细胞、细胞毒性T淋巴细胞和常规1型树突状细胞。
此外,瘤内给予FOLactis在多种免疫细胞浸润不良及抗PD1耐药的肿瘤中诱导了更强的肿瘤抗原特异性免疫应答和更优的全身抗肿瘤疗效。对不同免疫细胞的特异性清除揭示,CD8+ T细胞和NK 细胞对于原位疫苗诱导的肿瘤消退至关重要。
我们的结果证实,FOLactis表现出增强的抗肿瘤免疫,并成功将“冷”肿瘤转化为“热”肿瘤。
In situ vaccination is a promising strategy to convert the immunosuppressive tumor microenvironment into an immunostimulatory one with limited systemic exposure and side effect.
However, sustained clinical benefits require long-term and multidimensional immune activation including innate and adaptive immunity.
Here, we develop a probiotic food-grade Lactococcus lactis-based in situ vaccination (FOLactis) expressing a fusion protein of Fms-like tyrosine kinase 3 ligand and co-stimulator OX40 ligand. Intratumoural delivery of FOLactis contributes to local retention and sustained release of therapeutics to thoroughly modulate key components of the antitumour immune response, such as activation of natural killer cells, cytotoxic T lymphocytes, and conventional-type-1-dendritic cells in the tumors and tumor-draining lymph nodes.
In addition, intratumoural administration of FOLactis induces a more robust tumor antigen-specific immune response and superior systemic antitumour efficacy in multiple poorly immune cell-infiltrated and anti-PD1-resistant tumors. Specific depletion of different immune cells reveals that CD8 + T and natural killer cells are crucial to the in situ vaccine-elicited tumor regression.
Our results confirm that FOLactis displays an enhanced antitumour immunity and successfully converts the 'cold' tumors to 'hot' tumors.
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