GPNMB CAR-T 细胞对胶质母细胞瘤的肿瘤-髓系双重靶向
Dual tumour-myeloid targeting of glioblastoma with GPNMB CAR-T cells.
胶质母细胞瘤是一种致死性脑肿瘤,目前的多模式治疗很少能阻止其复发。
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Dual tumour-myeloid targeting of glioblastoma with GPNMB CAR-T cells.
胶质母细胞瘤是一种致死性脑肿瘤,目前的多模式治疗很少能阻止其复发。
uPAR is highly expressed in recurrent glioblastoma and represents a candidate CAR T cell target.
这些数据共同表明,靶向 uPAR 在 GBM 中具有效力与治疗潜力。
Glioblastoma stem cells as carriers of tumour memory: a strategy for personalised immunotherapy using tumour-infiltrating lymphocytes.
胶质母细胞瘤(GB)仍然是最具侵袭性的脑肿瘤之一,中位生存期为15个月,这主要归因于对现有抗癌疗法(包括前沿免疫疗法)的耐药性。
LAK to CIK continuum in glioma immunotherapy: a systematic review of efficacy and safety outcomes.
LAK和CIK疗法对胶质瘤患者均可能有益,其中CIK更安全且与更高的疗效相关。尽管需要更大规模的临床试验来巩固所观察到的结果。
Immune cell infiltration into brain tumor microenvironment is mediated by Rab27-regulated vascular wall integrity.
侵袭性脑肿瘤常表现出免疫“冷”微环境,其中血管屏障以尚不明确的方式阻碍有效免疫治疗。
Bacterial RNA downregulates MHC-I in tumor cell lines, promoting NK response and delaying tumor growth.
我们建立的MHC-I下调模型(通过bacRNA或合成hTLR8激动剂)可作为促进抗肿瘤反应的治疗策略。
New approaches to targeted drug therapy of intracranial tumors.
颅内肿瘤涵盖一组异质性肿瘤,包括胶质瘤、脑膜瘤、垂体腺瘤、神经鞘瘤、颅咽管瘤、室管膜瘤、髓母细胞瘤和原发性中枢神经系统淋巴瘤。
PTPN1/PTPN2 inhibition improves NK cancer therapy by enhancing IL-2 and mitigating TGFβ1 responses.
自然杀伤(NK)细胞是同种异体抗肿瘤免疫治疗有前景的候选细胞。
Functional profiling of murine glioma models highlights targetable immune evasion phenotypes.
癌症内在的免疫逃逸机制和多效性是癌症免疫治疗的障碍。
Clinical translation of mRNA-based cancer vaccines for solid tumors.
使用信使RNA(mRNA)的疫苗已成为一个有前景的平台,正在改变癌症免疫治疗。
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