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:An in vivo combined induction strategy of whole cancer cell vaccines triggers systemic immunity to eradicate triple-negative breast cancer.
An in vivo combined induction strategy of whole cancer cell vaccines triggers systemic immunity to eradicate triple-negative breast cancer.
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三阴性乳腺癌(TNBC)是乳腺癌中最具挑战性的亚型,面临化疗毒性和免疫相关不良事件的临床挑战。传统的治疗性癌症疫苗毒性相对较低,但由于缺乏疫苗免疫原性也未能成功。
在此,我们基于唾液酸(SA)-L-选择素轴介导的体内活细胞纳米药物递送系统(LCNDDS),开发了一种全癌细胞疫苗(WCVs)的体内联合诱导策略。抗原诱导剂(蜂毒肽和米托蒽醌)通过体内LCNDDS精准靶向肿瘤,并共同促进肿瘤抗原的全面释放,尤其是肿瘤细胞膜抗原。该过程激活了树突状细胞和辅助性T淋巴细胞,耗竭了髓源性抑制细胞,并产生了活性细胞毒性T淋巴细胞和NK 细胞,从而显示出“擎天柱”般的肿瘤抑制指数。
此外,WCVs在体内共诱导几乎根除了早期和晚期TNBC,延长了小鼠的生存期,并建立了强大的免疫记忆以防止晚期癌症的继发性败血症,具有优异的生物安全性。
总之,基于SA-L-选择素轴的WCVs体内联合诱导策略可以触发全身免疫激活以根除TNBC。我们的发现为解决TNBC的临床挑战提供了一种新策略。
Triple-negative breast cancer (TNBC) represents the most challenging subtypes of breast cancer, facing the clinical challenges of chemotherapeutic toxicity and immune related adverse events. Traditional therapeutic cancer vaccines, which have relatively low toxicity, also fail, due to a lack of vaccine immunogenicity.
Herein, we developed an in vivo combined induction strategy of whole cancer cell vaccines (WCVs), based on sialic acid (SA)-L-selectin axis-mediated in vivo live-cell nano-drug delivery system (LCNDDS). Antigen inducers (melittin and mitoxantrone) precisely targeted tumors via the in vivo LCNDDS, and collectively facilitated the whole release of tumor antigens, particularly tumor cell membrane antigens.
This process activated dendritic cells and helper T lymphocytes, depleted myeloid-derived suppressor cells, and generated active cytotoxic T lymphocytes and natural killer cells, thereby showing an "optimus prime" tumor inhibition index.
Furthermore, the WCVs co-induced in vivo nearly eradicated both early and advanced TNBC, extended the survival of mice, and established robust immune memory to prevent secondary sepsis in advanced cancer, with excellent biological safety. In summary, the in vivo combined induction strategy of WCVs based on SA-L-selectin axis can trigger systemic immune activation to eradicate TNBC.
Our findings present a novel strategy for addressing the clinical challenges of TNBC.
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