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.
我们的工作确立了CD81作为连接放射抵抗与免疫逃逸的关键桥梁,其通过维持GBM中CD274的丰度发挥作用,并突显CD81作为优化放射免疫治疗的有前景的治疗靶点。
英文原题:Personalized Cancer Vaccines in the Clinical Trial Pipeline.
Personalized Cancer Vaccines in the Clinical Trial Pipeline.
目前有广泛的早期个性化癌症疫苗管线正在针对多种癌症类型进行临床试验。
概述目前正在进行临床开发的个体化癌症疫苗,旨在提高认识并促进学术、商业研究人员和非营利社区之间的合作。
截至2024年11月25日,利用ClinicalTrials.gov数据库生成了78项个性化癌症疫苗临床试验的数据集。我们基于申办方、疾病、阶段、疫苗类型和全球地理分布对这些研究进行了分析。
大多数试验集中在肽疫苗(40%)和树突状细胞疫苗(19%),靶向实体瘤、脑癌、胰腺癌和乳腺癌等。1期试验占主导地位,占研究的90%以上,在美国(44%)和中国(24%)有显著活动。行业赞助商支持了22%的研究。活跃试验占数据集的72%,反映了该领域正在进行的研究工作。入组规模差异很大,从少于10名参与者的小型探索性队列到入组多达700名患者的大型试验不等。已完成评估各种癌症类型个性化新抗原疫苗的临床试验显示,疫苗通常耐受性良好,引发强烈的T细胞反应,并产生有希望的临床结果,如肿瘤缩小或延长PFS,特别是在黑色素瘤、胶质母细胞瘤和尿路上皮癌中,尽管未证明有普遍治愈方法。
AIM: To present an overview of personalized cancer vaccines currently undergoing clinical development, aiming to enhance awareness and promote collaboration among academic, commercial researchers, and non-profit communities. METHODS: A dataset of 78 clinical trials for personalized cancer vaccines was generated using ClinicalTrials.gov database as of November 25, 2024. We conducted an analysis of the studies based on sponsors, conditions, phases, types of vaccines, and global geographic distribution. RESULTS: The majority of trials focused on peptide vaccines (40%) and dendritic cell vaccine (19%), targeting solid tumors, brain, pancreatic and breast cancers, among others. Phase 1 trials dominated the landscape, accounting for over 90% of studies, with significant activity in the United States (44%) and China (24%). Industry sponsors backed 22% of studies. Active trials represented 72% of the dataset, reflecting ongoing research efforts in this field. Enrollment sizes varied widely, ranging from small exploratory cohorts of fewer than 10 participants to larger-scale trials enrolling up to 700 patients. Completed clinical trials evaluating personalized neoantigen vaccines across various cancer types showed that vaccines were generally well-tolerated, elicited strong T-cell responses, and resulted in promising clinical outcomes such as tumor shrinkage or prolonged progression-free survival, particularly in melanoma, glioblastoma, and urothelial cancer, although no universal cure was demonstrated. CONCLUSIONS: There is a broad early-stage pipeline of personalized cancer vaccines currently being tested in clinical trials for various cancer types.
MEMBER ACCOUNT
登录成功会直接打开下一页。