γδ T 细胞调节小细胞肺癌中的抗肿瘤免疫
γδ T cells modulate anti-tumor immunity in small cell lung cancer.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Modulated electro-hyperthermia enhances tumor cell susceptibility to γδ T cell-mediated cytotoxicity and tumor infiltration in NOD/SCID xenograft models.
Modulated electro-hyperthermia enhances tumor cell susceptibility to γδ T cell-mediated cytotoxicity and tumor infiltration in NOD/SCID xenograft models.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
这些发现提示 mEHT 可能增强肿瘤细胞对γδ T 细胞介导的细胞毒作用的敏感性,并可能促进免疫细胞浸润。这些效应可能涉及 mEHT 诱导的热效应和非热生物学反应。因此,本研究提供了概念验证,即 mEHT 与基于γδ T 细胞的免疫治疗联合可能是一种有前景的策略,值得进一步的机制和转化研究。
大量研究报道γδ T细胞疗法是一种有前景的癌症免疫治疗策略;然而,其疗效仍受限于肿瘤浸润不足和靶细胞易感性。调制电热疗(mEHT)是一种局部区域热疗方式,可选择性地向肿瘤组织传递调幅射频能量,并可能诱导热效应和非热生物效应。
在本研究中,我们探讨了mEHT是否能增强肿瘤细胞对γδ T细胞介导的细胞毒作用的敏感性,并促进免疫细胞浸润。人γδ T细胞经体外扩增后,与经mEHT或传统水浴加热预处理的肿瘤细胞共培养。
mEHT处理后的肿瘤细胞对γδ T细胞介导的细胞毒性表现出显著增强的敏感性,与对照组相比。在荷HepG2异种移植瘤的NOD/SCID小鼠中,局部mEHT治疗随后静脉注射γδ T细胞,与任一单一疗法相比,均显著抑制了肿瘤生长并增加了瘤内CD3+ T细胞浸润。每个实验组由六只小鼠组成。
Numerous studies have reported γδ T cell therapy as a promising immunotherapeutic strategy for cancer treatment; however, its efficacy remains limited by insufficient tumor infiltration and target cell susceptibility. Modulated electro-hyperthermia (mEHT) is a loco-regional hyperthermia modality that selectively delivers amplitude-modulated radiofrequency energy to tumor tissues and may induce both thermal and non-thermal biological effects.
In this study, we investigated whether mEHT could enhance tumor cell susceptibility to γδ T cell-mediated cytotoxicity and promote immune cell infiltration. Human γδ T cells were expanded ex vivo and co-cultured with tumor cells pretreated with mEHT or conventional water bath heating.
mEHT-treated tumor cells exhibited significantly increased susceptibility to γδ T cell-mediated cytotoxicity compared with controls. In HepG2 xenograft-bearing NOD/SCID mice, local mEHT treatment followed by intravenous injection of γδ T cells resulted in significantly suppressed tumor growth and increased intratumoral CD3 + T cell infiltration compared with either monotherapy. Each experimental group consisted of six mice.
Taken together, these findings suggest that mEHT may enhance tumor cell susceptibility to γδ T cell-mediated cytotoxicity and may facilitate immune cell infiltration. These effects could potentially involve both thermal and non-thermal biological responses induced by mEHT. This study therefore provides proof-of-concept that combining mEHT with γδ T cell-based immunotherapy may be a promising strategy that warrants further mechanistic and translational investigation.
MEMBER ACCOUNT
登录成功会直接打开下一页。