开发基于溶瘤病毒递送 CD19 和 EGFRvIII 抗原与双特异性 CAR 的胶质母细胞瘤多模式治疗
Developing a multimodal therapy for glioblastoma using oncolytic virus delivering CD19 and EGFRvIII antigens and bi-specific CARs.
肿瘤细胞治疗研究
FRONTIER PAPERS
近 5 年肿瘤细胞治疗领域的研究论文。默认按评分排序(权威性 + 新鲜度)。
Developing a multimodal therapy for glioblastoma using oncolytic virus delivering CD19 and EGFRvIII antigens and bi-specific CARs.
Mediation Mendelian randomization analysis of immune cell phenotypes and glioma risk: unveiling the regulation of cerebrospinal fluid metabolites.
本研究识别出特定免疫细胞表型直接影响胶质瘤风险,并通过脑脊液代谢物间接调控该风险。IgD(+) CD24(-) B 细胞上的 CD19 被确定为风险因素,而单核细胞上的 CD11c 具有保护作用。7-hoca 和甘油磷酸肌醇等代谢物发挥关键中介作用。这些发现增进了我们对胶质瘤病理生理学的理解,并提示免疫调节和代谢干预可能是具有前景的治疗策略。
Enhancing anti-EGFRvIII CAR T cell therapy against glioblastoma with a paracrine SIRPγ-derived CD47 blocker.
Progesterone boosts abiraterone-driven target and NK cell therapies against glioblastoma.
Prog 与 Abi 的联合是一种有前景的 GBM 治疗策略,在抑制肿瘤生长、延长生存和调节免疫微环境方面显示出潜力。
CD19 CAR-expressing iPSC-derived NK cells effectively enhance migration and cytotoxicity into glioblastoma by targeting to the pericytes in tumor micr
Application of blood brain barrier models in pre-clinical assessment of glioblastoma-targeting CAR-T based immunotherapies.
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