用高效的瘤抗原涂层设计的沙门氏菌免疫疗法建立了抗原特异性CD8+T细胞免疫力,并增加了I型干扰素联合治疗的抗瘤疗效
Suyang Wang1, Michelle Cheng1, Chao-Cheng Chen1
1Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Oncoimmunology
|January 3, 2024
概括
这项研究开发了沙门氏菌-9RE7 (Sal-9RE7) 细菌,用于增强癌症免疫治疗. 与蛋白-IFNβ (Alb-IFNβ) 联合治疗显著增强了瘤微环境中的抗瘤效果和免疫反应.
科学领域:
- 免疫学 免疫学 免疫学
- 微生物学 微生物学
- 在瘤学瘤学.
背景情况:
- 基于细菌的癌症治疗利用瘤相关抗原 (TAA) 刺激针对瘤的特定免疫力.
- 以前的抗原递送策略在抗原呈现效率方面遇到了局限性.
研究的目的:
- 开发一种改进的细菌疫苗用于癌症免疫疗法,使用一种新的抗原结合方法.
- 评估工程沙门氏菌疫苗,沙门氏菌-9RE7 (Sal-9RE7) 的疗效,作为单疗法和与辅助剂结合使用.
主要方法:
- 改造沙门氏菌SL7207以在其外膜上显示聚氨酸扩展的HPV E7抗原 (9RE7),从而产生Sal-9RE7.7.
- 在TC-1瘤小鼠模型中,Sal-9RE7作为单疗法和与阿尔伯明-IFNβ (Alb-IFNβ) 辅助剂联合使用.
- 评估瘤生长,抗原特异性免疫力和瘤微环境 (TME) 内的免疫性.
主要成果:
- 与以前的方法相比,Sal-9RE7显示出显著改善的抗原呈现.
- 单一治疗Sal-9RE7有效地通过诱导E7抗原特异性免疫来降低瘤生长.
- 与Alb-IFNβ联合治疗显著提高了TME的抗瘤疗效和免疫性.
结论:
- 开发的Sal-9RE7细菌疫苗代表了TAA输送的个性化免疫疗法的重大进步.
- 与Alb-IFNβ的联合治疗为增强瘤微环境中的抗瘤反应提供了一个有希望的策略.
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