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:Natural killer cells: unlocking new treatments for bladder cancer.
Natural killer cells: unlocking new treatments for bladder cancer.
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非肌层浸润性膀胱癌是一种拥有最古老免疫治疗标准疗法的疾病,近期通过应用检查点阻断抗体在治疗方面取得了进展。遗憾的是,尽管通过生物标志物进行了分层,对程序性细胞死亡蛋白1(PD-1)和程序性死亡配体1(PD-L1)阻断抗体的缓解率仍然很低。自然杀伤(NK)细胞与T细胞具有共同的生物学特性,但缺乏真正的抗原特异性,并且对致瘤威胁反应更早,因此是联合免疫治疗的理想靶点。正在临床研究中的NK靶向免疫疗法,包括抗NKG2A抗体、白细胞介素激动剂和工程化病毒载体,有望改变膀胱癌的免疫治疗格局,并将成为本综述的重点。
Non-muscle invasive bladder cancer, a disease with the oldest immunotherapeutic standard of care, has seen recent improvements in treatment via the application of checkpoint blocking antibodies. Unfortunately, response rates to programmed cell death protein 1 (PD-1) and programmed death-ligand 1 (PD-L1) blocking antibodies remain low despite stratification by biomarkers.
Sharing common biology with T cells but lacking true antigen-specificity and responding earlier to tumorigenic threats, natural killer (NK) cells present an ideal target for combination immunotherapies. NK-targeted immunotherapies under clinical investigation, including anti-NKG2A antibodies, interleukin agonists, and engineered viral vectors, hold promise in altering the immunotherapeutic landscape in bladder cancer and will be the focus of this review.
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