CD81 通过阻断 CD274/PD-L1 的选择性自噬降解驱动放射抵抗性胶质母细胞瘤的免疫逃逸
CD81 drives immune evasion in radioresistant glioblastoma by blocking selective autophagic degradation of CD274/PD-L1.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Immunotherapy with autologous dendritic cells in the complex treatment of malignant gliomas - results.
Immunotherapy with autologous dendritic cells in the complex treatment of malignant gliomas - results.
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在恶性胶质瘤患者复杂治疗方案中应用免疫治疗,在总生存期和无复发生存期中位数方面显示出明显的积极趋势。但尽管如此,免疫治疗作为一种治疗工具仍需进一步发展、研究和改进,这需要考虑恶性胶质瘤中的免疫抑制及其克服手段,在靶抗原选择、细胞制备以及树突状疫苗与其他治疗方案的整合方面进行优化。
评估树突状细胞疫苗在恶性脑胶质瘤患者综合治疗结构中的有效性,并与治疗结构中未接受免疫治疗的对照组患者进行比较。
在一项单中心、前瞻性、队列研究中,以prof. A.L. Polenov命名的RNSI为基础开展,共有91例经形态学确诊的恶性胶质瘤(胶质母细胞瘤)患者参与。主要组为41例患者,除标准治疗(手术、放疗和化疗)外,还接受了特异性抗肿瘤免疫治疗。50例患者仅接受标准治疗,未接受免疫治疗。
免疫治疗组的中位生存期为21.7个月(95% CI 4-37个月),非免疫治疗组为15.8个月(95% CI 3-22个月)(p = 0.002)。免疫治疗组的中位无复发生存期为13.8个月(95% CI 1-20个月),非免疫治疗组为7.9个月(95% CI 1-12个月)(p = 0.003)。
Evaluation of the effectiveness of dendritic cell vaccine in patients with malignant brain gliomas in the structure of complex treatment in comparison with the control group of patients without immunotherapy in the structure of treatment.
In a single-center, prospective, cohort study, taking place on the basis of the RNSI named after prof. A.L. Polenov, 91 patients with morphologically established malignant glial tumor (glioblastoma) took part. The main group of 41 patients who, in addition to standard treatment (surgical, radiation and chemotherapy), underwent specific antitumor immunotherapy. 50 patients received only standard treatment, without immunotherapy.
Median survival was 21.7 months in the immunotherapy group (95% CI 4-37 months) and 15.8 months (95% CI 3-22 months) in the non-immunotherapy group (p = 0.002). The median relapse-free period in the group with immunotherapy was 13.8 months (95% CI 1-20 months), and in the group without immunotherapy 7.9 months (95% CI 1-12 months) (p = 0.003).
In general, the use of immunotherapy in the structure of complex treatment of patients with malignant gliomas demonstrates a clear positive trend in terms of overall survival and median relapse-free period. But nevertheless, immunotherapy requires further development as a therapeutic tool, study and improvement, which will take into account immunosuppression in malignant gliomas and means of overcoming it, optimization in terms of target antigen selection, cell preparation and integration of dendritic vaccines into other treatment regimens.
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