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:Cell-Surface GRP78-Targeted Chimeric Antigen Receptor T Cells Eliminate Lung Cancer Tumor Xenografts.
Cell-Surface GRP78-Targeted Chimeric Antigen Receptor T Cells Eliminate Lung Cancer Tumor Xenografts.
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肺癌是最常见且最难治的恶性肿瘤之一。尽管现有治疗方法存在,但其生存率仍然很低,这表明迫切需要新的、更有效的疗法,例如CAR-T(CAR-T)细胞免疫疗法。细胞表面葡萄糖调节蛋白78(csGRP78)在多种血液系统恶性肿瘤和包括肺癌在内的实体瘤细胞中因癌症相关内质网应激而表达,而GRP78则局限于正常细胞内部。
在此,我们通过免疫荧光检测到csGRP78在两种肺癌细胞系A549和H1299以及源自A549的癌症干样细胞中均有显著表达。接下来,我们构建了靶向csGRP78的CAR,并检测了转导后的CAR-T 细胞杀伤这两种肺癌细胞系及衍生干样细胞的能力,该能力与体外特异性干扰素释放相关。
最后,我们发现csGRP78 CAR-T 细胞也能有效杀伤肺癌细胞和癌症干样细胞,从而在体内消除肿瘤异种移植瘤,在肿瘤清除后63天内既无任何复发证据,也未对我们检查的其他身体器官产生任何有害影响。
我们的研究揭示了csGRP78作为治疗靶点的能力,并为开发csGRP78 CAR-T 细胞作为肺癌潜在疗法提供了有价值的见解。
Lung cancer is one of the most common and intractable malignancies. It is associated with low survival rates despite existing treatments, indicating that new and more effective therapies are urgently needed such as the chimeric antigen receptor-T (CAR-T) cell immunotherapy. The cell-surface glucose-regulated protein 78 (csGRP78) is expressed in various hematological malignancies and solid tumor cells including lung cancer in response to cancer-related endoplasmic reticulum stress, while GRP78 is restricted to inside the normal cells.
Here, we detected the prominent expression of csGRP78 in both lung cancer cell lines, A549 and H1299, as well as cancer stemlike cells derived from A549 by immunofluorescence. Next, a csGRP78-targeted CAR was constructed, and the transduced CAR-T cells were tested for their potency to kill the two lung cancer cell lines and derived stemlike cells, which was correlated with specific interferon release in vitro.
Finally, we found that csGRP78 CAR-T cells also efficiently killed both lung cancer cells and cancer stemlike cells, resulting into the elimination of tumor xenografts in vivo, neither with any evidence of relapse after 63 days of tumor clearance nor any detrimental impact on other body organs we examined.
Our study reveals the capacity of csGRP78 as a therapeutic target and offers valuable insight into the development of csGRP78 CAR-T cells as potential therapy for lung cancer.
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