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Positive allosteric modulators of the PD-1•PD-L1 interaction as a new mode of therapeutic intervention for autoimmune diseases: preclinical proof of concept in humanized mice

Project description

Allosteric modulation of immune checkpoints for autoimmunity

Immune checkpoints are key regulatory molecules that modulate immune responses to maintain balance and prevent autoimmunity. Conventional drugs inhibiting these molecules have been explored for cancer therapy and autoimmune diseases. The ERC-funded PAMinMICE project will explore an entirely new strategy through the development of positive allosteric modulators (PAMs) that enhance checkpoint signalling. PAMs stabilise the interaction between checkpoint receptors and ligands, thereby promoting the suppression of immune responses prominent in autoimmune diseases. Researchers will test this pioneering approach in humanised mouse models of lupus, psoriasis and colitis. Project findings will pave the way towards a novel therapeutic avenue for autoimmune diseases.

Objective

The immune system's balance in fighting infections or cancer while avoiding autoimmune reactions is regulated by co-inhibitory and co-stimulatory immune checkpoints (ICs). ICs are major drug targets in immunotherapy, with antibodies (Abs) blocking inhibitory ICs to fight cancer, and Abs blocking stimulatory ICs in clinical trials for autoimmune diseases.
Surprisingly, but likely fuelled by the worldwide focus on IC inhibitors, the field largely ignored that ICs are genuine transmembrane receptors that transmit signals upon binding of an extracellular ligand. This leaves unexplored modes of therapeutic intervention that we uncover in my granted ERC-2023-ADG by validating allosteric Nanobodies (Nbs) that bind and stabilize ICs, to agonize their activity as first-in-class allosteric modulators, thus tipping the immune homeostasis balance opposite to IC inhibitors for treating autoimmunity.
Recently, we discovered the first-ever positive allosteric modulators (PAMs) of an IC and characterized several PAMs of the human PD-1•PD-L1 complex that agonize PD-L1 binding to PD-1 (affinity) and stimulate IC signalling (efficacy) in a spatio-temporal-selective and pathway-selective manner. Building on these exceptional proof of concept data, I’m founding our next integrated drug discovery company focussing on allosteric immunotherapies as a new mode of therapeutic intervention.
With PAMinMICE, I will perform pioneering experiments in animal models and test positive allosteric modulation of the PD-1•PD-L1 interaction in double-humanized PD-1•PD-L1 knock-in mice as a new mode of therapeutic intervention for diverse autoimmune diseases: psoriasis, colitis, atopic dermatitis, lupus, rheumatoid arthritis. This study may provide the first preclinical evidence supporting the use of allosteric modulators targeting inhibitory ICs for treating such disorders, with the goals of (i) benefiting patients, (ii) strengthening our IP portfolio, and (iii) positioning us for successful fundraising toward the spin-off.

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Topic(s)

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Funding Scheme

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HORIZON-ERC-POC - HORIZON ERC Proof of Concept Grants

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Call for proposal

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(opens in new window) ERC-2025-POC

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Host institution

VIB VZW
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.

€ 150 000,00
Address
SUZANNE TASSIERSTRAAT 1
9052 ZWIJNAARDE - GENT
Belgium

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Region
Vlaams Gewest Prov. Oost-Vlaanderen Arr. Gent
Activity type
Research Organisations
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Total cost

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Beneficiaries (1)

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