决定异体 CAR T 细胞排斥与扩增的细胞和分子机制
Cellular and molecular mechanisms determining allogeneic CAR T cell rejection and expansion.
我们评估了11例接受单一批次cemacabtagene ansegedleucel(cema-cel)治疗的大B细胞淋巴瘤患者,cemacabtagene ansegedleucel是一种异体抗CD19 CAR T产品。
英文原题:Novel perspectives on MSLN-targeted cancer therapy: from molecular mechanisms to clinical translation.
间皮素(MSLN)是一种糖基磷脂酰肌醇(GPI)锚定的膜蛋白,通过激活MAPK/ERK和PI3K/AKT等多条信号通路,促进肿瘤细胞增殖、迁移和免疫逃逸等恶性行为。
间皮素(MSLN)是一种糖基磷脂酰肌醇(GPI)锚定的膜蛋白,通过激活MAPK/ERK和PI3K/AKT等多条信号通路,促进肿瘤细胞增殖、迁移和免疫逃逸等恶性行为。MSLN在恶性肿瘤中广泛过表达,但在正常组织中表达水平较低。这种差异表达模式使MSLN成为重要的临床治疗靶点。目前,基于MSLN的肿瘤靶向策略主要涉及抗体药物偶联物(ADC)、癌症疫苗、溶瘤病毒和CAR-T 细胞疗法。这些治疗方式在临床前研究和I/II期临床试验中已显示出令人鼓舞的疗效。然而,MSLN信号通路分子机制不明确以及胞外域脱落等挑战限制了靶向治疗策略。因此,本综述全面讨论了MSLN的基因和蛋白结构、其生物学功能及相关靶向治疗策略,为MSLN靶向癌症治疗提供了新的见解。
Mesothelin (MSLN) is a glycosylphosphatidylinositol (GPI)-anchored membrane protein that promotes malignant behaviors including tumor cell proliferation, migration and immune evasion through activation of multiple signaling pathways, such as MAPK/ERK and PI3K/AKT. MSLN is widely overexpressed in malignant tumors but shows low expression levels in normal tissues. This differential expression pattern renders MSLN an important clinical therapeutic target. Currently, MSLN-based tumor-targeting approaches predominantly involve antibody-drug conjugates (ADC), cancer vaccines, oncolytic viruses and chimeric antigen receptor T-cell (CAR-T) therapies. These therapeutic modalities have demonstrated encouraging efficacy in preclinical studies and phase I/II clinical trials. However, challenges such as unclear molecular mechanisms of MSLN signaling pathways and extracellular domain shedding impose limitations on targeted therapeutic strategies. Therefore, this review comprehensively discusses the gene and protein structures of MSLN, its biological functions, and related targeted therapeutic strategies, providing new insights into MSLN-targeted cancer therapy.
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