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CD2 增强通过免疫突触重塑和减轻 T 细胞耗竭增强 CAR-T 细胞疗效

英文原题:CD2 augmentation enhances CAR-T-cell efficacy via immunological synapse remodeling and T-cell exhaustion mitigation.

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CD2 augmentation enhances CAR-T-cell efficacy via immunological synapse remodeling and T-cell exhaustion mitigation.

PubMed 2025/07/04(内容时间) Cell Mol Immunol Q1 · IF 23.9(JCR 2025)

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中文摘要

CAR-T 细胞疗法在治疗血液恶性肿瘤方面取得了重大进展,但其疗效往往受到T细胞功能欠佳的限制,表现为抗肿瘤能力弱和缺乏持久性。免疫突触是T细胞功能的关键决定因素,受CD58-CD2轴影响。T细胞上CD2表达的动态调控影响CAR介导的免疫突触质量,进而影响CAR-T 细胞的功能结局和分化。我们的研究表明,CD2表达水平与CAR-T 细胞形成的免疫突触质量及其抗肿瘤效力密切相关。外源性CD2补充增强CAR-T 细胞形成高质量突触的能力,减少T细胞耗竭,并提高持续抗肿瘤疗效。此外,异位CD2表达增加CAR-T 细胞对低密度抗原的敏感性。因此,在CAR-T 细胞中补充CD2是提高CAR-T 细胞疗法疗效的一种有前景的策略。

展开英文摘要原文

CAR-T-cell therapy has made significant strides in treating hematological malignancies, yet its efficacy is often hampered by suboptimal T-cell functionality, marked by weak antitumor capabilities and a lack of durability. The immunological synapse, a key determinant of T-cell function, is influenced by the CD58-CD2 axis. The dynamic regulation of CD2 expression on T cells impacts the quality of CAR-mediated immunological synapses, affecting CAR-T-cell functional outcomes and differentiation.

Our study demonstrated that CD2 expression levels are closely linked to the quality of immunological synapses formed by CAR-T cells and their antitumor potency. Exogenous CD2 supplementation enhances the ability of CAR-T cells to form high-quality synapses, reduces T-cell exhaustion, and increases sustained antitumor efficacy.

Additionally, ectopic CD2 expression increases CAR-T-cell sensitivity to low-density antigens.

Thus, replenishing CD2 in CAR-T cells is a promising strategy to increase the therapeutic efficacy of CAR-T-cell therapy.

论文信息

作者
Zhu Q、Li J、Liu N、Han L、Wu Z、Wang Y、Lin X、Wei J
第一作者单位
Department of Biotherapy, the First Medical Center, Chinese PLA General Hospital, Beijing, China.China
通讯作者单位
Department of Biotherapy, the First Medical Center, Chinese PLA General Hospital, Beijing, China. hanwdrsw@163.com.China
文献类型
非美国政府资助研究
期刊
Cellular & molecular immunology2025 Aug
原文标识
PubMed 40615696 · DOI 10.1038/s41423-025-01314-6