CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Recent progress in targeting the sialylated glycan-SIGLEC axis in cancer immunotherapy.
Recent progress in targeting the sialylated glycan-SIGLEC axis in cancer immunotherapy.
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恶性肿瘤是由癌细胞和肿瘤微环境细胞组成的复杂结构。在这一复杂结构中,细胞相互交流并相互作用,从而共同促进癌症的发展和转移。近年来,基于免疫调节分子的癌症免疫治疗极大地提高了实体癌的治疗效果,从而使部分患者能够实现持久缓解或治愈。然而,由于耐药性的产生和低缓解率,针对现有靶点 PD-1/PD-L1 或 CTLA-4 的免疫治疗获益有限。尽管已提出联合治疗以提高缓解率,但观察到严重的不良反应。因此,必须寻找替代性免疫检查点。SIGLEC 是近年来发现的一类免疫调节受体(被称为糖免疫检查点)。本综述系统描述了 SIGLEC 的分子特征,并讨论了合成配体、单克隆抗体抑制剂和CAR-T(CAR-T)细胞等领域的最新进展,重点关注阻断唾液酸化聚糖-SIGLEC 轴的可用策略。靶向糖免疫检查点可以扩展免疫检查点的范围,并为新药开发提供多种选择。
Malignant tumors are complex structures composed of cancer cells and tumor microenvironmental cells. In this complex structure, cells cross-talk and interact, thus jointly promoting cancer development and metastasis. Recently, immunoregulatory molecule-based cancer immunotherapy has greatly improved treatment efficacy for solid cancers, thus enabling some patients to achieve persistent responses or cure.
However, owing to the development of drug-resistance and the low response rate, immunotherapy against the available targets PD-1/PD-L1 or CTLA-4 has limited benefits. Although combination therapies have been proposed to enhance the response rate, severe adverse effects are observed.
Thus, alternative immune checkpoints must be identified. The SIGLECs are a family of immunoregulatory receptors (known as glyco-immune checkpoints) discovered in recent years.
This review systematically describes the molecular characteristics of the SIGLECs, and discusses recent progress in areas including synthetic ligands, monoclonal antibody inhibitors, and Chimeric antigen receptor T (CAR-T) cells, with a focus on available strategies for blocking the sialylated glycan-SIGLEC axis. Targeting glyco-immune checkpoints can expand the scope of immune checkpoints and provide multiple options for new drug development.
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