与树突状细胞串联:设计先进 T 细胞免疫疗法的途径。

Frontiers in systems biology Pub Date : 2024-01-01 Epub Date: 2024-04-29 DOI:10.3389/fsysb.2024.1372995
Sogand Schafer, Kaige Chen, Leyuan Ma
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引用次数: 0

摘要

树突状细胞(DC)和 T 细胞之间的串联在调节自然和病理条件下的免疫反应中起着至关重要的作用。DC-T细胞之间的串联是通过依赖接触的机制(即免疫突触)和不依赖接触的机制(即细胞因子)实现的。活化的 DC 上调共刺激信号并分泌促炎细胞因子,以协调 T 细胞的活化和分化。相反,活化的 T 辅助细胞会 "许可 "DC 走向成熟,而调节性 T 细胞(Tregs)则会抑制 DC 以激发耐受性免疫。有效调节DC-T细胞串扰的策略可用于促进癌症免疫疗法的免疫激活或治疗自身免疫性疾病的免疫耐受。在此,我们回顾了 DC 和 T 细胞之间的天然串联机制。我们重点介绍了调节直流-T 细胞串联的生物工程方法,包括传统疫苗、合成疫苗和直流模拟物,以及利用这些方法引导免疫反应以治疗癌症和自身免疫性疾病的重要开创性研究。
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Crosstalking with Dendritic Cells: A Path to Engineer Advanced T Cell Immunotherapy.

Crosstalk between dendritic cells (DCs) and T cells plays a crucial role in modulating immune responses in natural and pathological conditions. DC-T cell crosstalk is achieved through contact-dependent (i.e., immunological synapse) and contact-independent mechanisms (i.e., cytokines). Activated DCs upregulate co-stimulatory signals and secrete proinflammatory cytokines to orchestrate T cell activation and differentiation. Conversely, activated T helper cells "license" DCs towards maturation, while regulatory T cells (Tregs) silence DCs to elicit tolerogenic immunity. Strategies to efficiently modulate the DC-T cell crosstalk can be harnessed to promote immune activation for cancer immunotherapy or immune tolerance for the treatment of autoimmune diseases. Here, we review the natural crosstalk mechanisms between DC and T cells. We highlight bioengineering approaches to modulate DC-T cell crosstalk, including conventional vaccines, synthetic vaccines, and DC-mimics, and key seminal studies leveraging these approaches to steer immune response for the treatment of cancer and autoimmune diseases.

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