间皮素作为癌症免疫治疗的生物标志物和治疗靶点
Mesothelin as Biomarker and Therapeutic Target for Immunotherapy in Cancer.
癌症仍是一个关键的全球健康问题,原因在于发现晚、耐药和高死亡率。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:The Efficacy of Neoantigen-Loaded Dendritic Cell Vaccine Immunotherapy in Non-Metastatic Gastric Cancer.
The Efficacy of Neoantigen-Loaded Dendritic Cell Vaccine Immunotherapy in Non-Metastatic Gastric Cancer.
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负载新抗原的 DC 疫苗可激发针对特定胃癌细胞肽的强免疫应答,并增强肿瘤细胞裂解,从而阻碍甚至逆转疾病进展,为胃癌患者的治疗提供了巨大潜力。
胃癌(GC)是全球癌症相关死亡的第三大原因。尽管手术和化疗是主要治疗手段,但免疫治疗,更具体地说是抗肿瘤疫苗接种,在过去几年中因其较低的相关毒性和较少的长期副作用而日益受到关注。树突状细胞(DC)疫苗已被证明可在体外和体内诱导肿瘤特异性细胞毒性T细胞(CTL)反应;然而,由于该疾病的特性,免疫治疗耐药性常常产生。各种修饰方法,如采用病毒载体、肿瘤RNA,甚至肿瘤特异性肽(新抗原),已被研究作为避免耐药性和增强疫苗有效性的手段。在本综述中,我们旨在评估负载新抗原的DC疫苗(naDCVs)对胃癌细胞免疫反应的影响。
在PubMed和ClinicalTrials.gov上进行了全面的文献检索,以评估naDCVs在体内和体外抗胃癌的疗效研究。两位独立评审员根据预定的纳入和排除标准对研究进行了资格评估。检索遵循PRISMA指南完成。
我们的系统综述纳入了11项研究。其中5项研究在体外测试了naDCV的效果;2项和4项研究分别在体外和体内进行了检测。体外研究表明,与对照组相比,研究组中naDCV对癌细胞产生了更强的免疫反应。在小鼠体内进行的研究表明,与未治疗组相比,接受naDCV治疗的组肿瘤体积减小。此外,疫苗组中CTL对肿瘤细胞的细胞毒性作用也增强。其中一项研究作为I期研究在人体中进行。结果显示,与对照组相比,接种组的CTL增殖和细胞因子产生增加,但在肿瘤大小方面未观察到差异。
A thorough literature search was conducted on PubMed and clinicaltrials.gov for studies assessing the efficacy of naDCVs against gastric cancer both in vivo and in vitro. The studies were assessed for eligibility by two independent reviewers based on predetermined inclusion and exclusion criteria. The search was completed following the PRISMA guidelines.
Eleven studies were included in our systematic review. In five of the studies, the effects of the naDCVs were tested in vitro; in two and in four they were examined both in vitro and in vivo. The in vitro studies showed that the naDCVs resulted in a more robust immune response against the cancer cells in the study groups compared to the control groups. The in vivo studies conducted on mice showed that tumor volume was reduced in the groups treated with the naDCV compared to the untreated groups. What is more, the cytotoxic effect of CTLs against tumor cells was also increased in the vaccine groups. One of the studies was conducted on humans as a phase I study. The results show increased CTL proliferation and cytokine production in the vaccinated group compared to the control, but no difference regarding the tumor size was observed.
Neoantigen-loaded DC vaccines can stimulate a strong immune response against specific gastric cancer cell peptides and enhance tumor cell lysis, therefore hindering or even reversing disease progression, offering great potential for the treatment of patients with gastric cancer.
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