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Engineering B cells to fight cancer

Project description

Engineered B cell immunotherapy in cancer treatment

In vivo B cell engineering to express therapeutic antibodies represents a safe and efficient method for the treatment of many conditions, including cancer. The presence of the tumour-specific B cells and anti-tumour antibodies in the plasma correlate with a favourable prognosis and response to treatment with checkpoint inhibitors in sarcomas and carcinomas. The EU-funded EngineerBcells project will develop a novel engineered B cell-based cancer immunotherapy using CRISPR/Cas9 and adeno-associated viral vectors to integrate the anti-tumour antibody genes into the IgH locus. The localised activation of engineered B cells will be demonstrated and evaluated in diverse tumour models. B cells will be co-engineered to secrete additional immune effectors upon activation.

Objective

B cells have an important role in the immune response against cancer. Tumor specific B cells in tertiary lymphoid structures and anti-tumor antibodies in the plasma are associated with a favorable prognosis and with an improved response to checkpoint inhibition in different sarcomas and carcinomas. Antigen specific B cells home to tumors and prolong survival in mice, while B cell based vaccines allow durable anti-tumor activity in cervical cancer patients. We have recently demonstrated both ex vivo and in vivo B cell engineering for the expression of anti-HIV antibodies. Here, we propose a novel cancer immunotherapy approach based on engineered B cells. In particular, we use CRISPR/Cas9 and AAV to target the integration of anti-tumor antibody genes into the IgH locus. In diverse tumor models, we plan to demonstrate localized B cell activation upon antigen engagement. The B cells will exert multiple anti-tumor effects. Secreted antibodies will induce ADCC, CDC and ADCP. In addition, a polyclonal T cell response with epitope spreading will be facilitated by engineered B cells acting as APCs as well as by antibodies forming immune complexes to be taken up by dendritic cells and macrophages for cross-presentation. The B cell will be co-engineered to locally secrete additional immune effectors upon activation. These include: stimulatory cytokines, BiTEs, checkpoint inhibitors, CD40/27 agonists and cell penetrating nanobodies. Localized secretion is predicted to increase efficacy while reducing systemic toxicities. When targeting self-antigens, B cells will be engineered to co-express a CAR, relaying CD40 or TLR signals for T cell independent B cell activation and allowing allogeneic therapy. We will further demonstrate in vivo B cell engineering for increased scalability, and ensure safety using a suicide cassette for inducible B cell elimination. B cell engineering is thus a flexible and robust platform technology that may revolutionize cancer immunotherapy.

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Keywords

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Programme(s)

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Topic(s)

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Funding Scheme

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HORIZON-ERC - HORIZON ERC Grants

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Call for proposal

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(opens in new window) ERC-2021-COG

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Host institution

TEL AVIV UNIVERSITY
Net EU contribution

Net EU financial contribution. The sum of money that the participant receives, deducted by the EU contribution to its linked third party. It considers the distribution of the EU financial contribution between direct beneficiaries of the project and other types of participants, like third-party participants.

€ 1 996 250,00
Total cost

The total costs incurred by this organisation to participate in the project, including direct and indirect costs. This amount is a subset of the overall project budget.

€ 1 996 250,00

Beneficiaries (1)

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