A novel enzyme-based therapeutic approach that reprograms immune cells from a pathogenic inflammatory state to homeostasis in multiple sclerosis (MS). Using indoleamine 2,3-dioxygenase 1 (IDO) delivered systemically as PEG-IDO or locally as an IDO-galectin-3 fusion protein, this therapy targets the tryptophan-kynurenine pathway to reduce Th17 cells, increase regulatory T cells, and reverse neurological symptoms in validated MS disease models.
This solution offers a new therapeutic strategy for multiple sclerosis (MS) that reprograms immune cells from a pathogenic inflammatory state back to immune homeostasis. The approach leverages the enzyme indoleamine 2,3-dioxygenase 1 (IDO), which catabolizes the essential amino acid tryptophan into kynurenine, a metabolite that activates the aryl hydrocarbon receptor (AhR) and promotes immune regulation.
Two delivery formats are being developed. Systemic PEG-IDO is designed to reprogram circulating immune cells before they traffic to the central nervous system (CNS). A localized fusion protein, IDO-galectin-3 (IDO-Gal3), binds to abundant tissue glycans to restrict diffusion and concentrate IDO activity at targeted inflamed tissues. In preclinical studies, retro-orbital injection of IDO-Gal3 crosses the leaky blood-brain barrier in inflamed CNS, similar to how intrathecal administration delivers therapies such as rituximab and baclofen in MS patients.
The therapeutic addresses a critical unmet need by reducing pathogenic Th17 CD4+ T cells in the CNS, increasing regulatory T cell (Treg) frequency, and reversing hind limb paralysis in validated MS mouse models without observed neurotoxicity.
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Key preclinical findings:
This technology is currently at the preclinical validation stage. Preliminary efficacy and safety data have been generated in the C57BL/6 chronic non-relapsing EAE mouse model, with demonstrated disease reversal, reduced CNS lesions, and no observed toxicity.
Future validation plans include expanded testing in three EAE models: a chronic non-relapsing model in C57BL/6 mice, a relapsing-remitting model in SJL mice, and a B cell-dependent EAE model. Studies will evaluate both disease prevention (at onset) and therapeutic intervention (at peak disease), along with detailed immunological mechanism studies and dose-escalation toxicology assessments. The approach builds on recent published findings and aims to establish dosing regimens for advancing toward clinical translation.
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