University of Cambridge, Cancer Research UK Cambridge Institute, Robinson Way, Cambridge, CB2 0RE, UK.
Astra Zeneca, Cambridge, UK.
EMBO Mol Med. 2024 Sep;16(9):2233-2261. doi: 10.1038/s44321-024-00121-2. Epub 2024 Aug 21.
We have developed and validated a highly specific, versatile antibody to the extracellular domain of human LGR5 (α-LGR5). α-LGR5 detects LGR5 overexpression in >90% of colorectal cancer (CRC), hepatocellular carcinoma (HCC) and pre-B-ALL tumour cells and was used to generate an Antibody-Drug Conjugate (α-LGR5-ADC), Bispecific T-cell Engager (α-LGR5-BiTE) and Chimeric Antigen Receptor (α-LGR5-CAR). α-LGR5-ADC was the most effective modality for targeting LGR5 cancer cells in vitro and demonstrated potent anti-tumour efficacy in a murine model of human NALM6 pre-B-ALL driving tumour attrition to less than 1% of control treatment. α-LGR5-BiTE treatment was less effective in the pre-B-ALL cancer model yet promoted a twofold reduction in tumour burden. α-LGR5-CAR-T cells also showed specific and potent LGR5 cancer cell killing in vitro and effective tumour targeting with a fourfold decrease in pre-B-ALL tumour burden relative to controls. Taken together, we show that α-LGR5 can not only be used as a research tool and a biomarker but also provides a versatile building block for a highly effective immune therapeutic portfolio targeting a range of LGR5-expressing cancer cells.
我们开发并验证了一种针对人 LGR5(α-LGR5)细胞外结构域的高度特异性、多功能抗体。α-LGR5 可检测超过 90%的结直肠癌(CRC)、肝细胞癌(HCC)和前 B 细胞急性淋巴细胞白血病(pre-B-ALL)肿瘤细胞中的 LGR5 过表达,并用其生成抗体药物偶联物(α-LGR5-ADC)、双特异性 T 细胞衔接器(α-LGR5-BiTE)和嵌合抗原受体(α-LGR5-CAR)。α-LGR5-ADC 在体外靶向 LGR5 癌细胞的效果最显著,并在人 NALM6 前 B-ALL 驱动的小鼠模型中显示出强大的抗肿瘤功效,使肿瘤负荷减少到对照治疗的 1%以下。α-LGR5-BiTE 治疗在前 B-ALL 癌症模型中的效果较差,但可使肿瘤负担减少两倍。α-LGR5-CAR-T 细胞在体外也显示出对 LGR5 癌细胞的特异性和强大杀伤作用,并能有效靶向肿瘤,与对照组相比,前 B-ALL 肿瘤负担减少了四倍。综上所述,我们证明了 α-LGR5 不仅可以作为研究工具和生物标志物,还为靶向一系列表达 LGR5 的癌细胞的高效免疫治疗组合提供了多功能构建模块。