Novel immunotherapeutics against LGR5 to target multiple cancer types
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Published:2024-08-21
Issue:9
Volume:16
Page:2233-2261
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ISSN:1757-4684
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Container-title:EMBO Molecular Medicine
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language:en
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Short-container-title:EMBO Mol Med
Author:
Chen Hung-Chang, Mueller Nico, Stott KatherineORCID, Kapeni Chrysa, Rivers Eilidh, Sauer Carolin MORCID, Beke FlavioORCID, Walsh Stephen J, Ashman Nicola, O’Brien Louise, Rafati Fard AmirORCID, Godsinia Arman, Li Changtai, Joud Fadwa, Giger Olivier, Zlobec Inti, Olan Ioana, Aitken Sarah JORCID, Hoare MatthewORCID, Mair RichardORCID, Serrao Eva, Brenton James DORCID, Garcia-Gimenez Alicia, Richardson Simon E, Huntly BrianORCID, Spring David RORCID, Skjoedt Mikkel-OleORCID, Skjødt Karsten, de la Roche MarcORCID, de la Roche MaikeORCID
Abstract
AbstractWe 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.
Funder
Cancer Research UK Wellcome Trust UKRI | Medical Research Council Pathological Society of Great Britain and Ireland
Publisher
Springer Science and Business Media LLC
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