Synthetic bioengineered macrophages for immune cell functions in infectious disease cellular therapy

Cutaneous leishmaniasis (CL) presents diverse clinical challenges due to species-specific drug efficacy and resistance. We propose a novel therapeutic strategy using synthetic biology to reprogram macrophage responses. By engineering an inducible TET-ON gene circuit to express immunomodulatory PeptideA (PepA), we enhance IL-12 production and parasite clearance. Peptides were identified via AI and validated through molecular dynamics simulations. This approach shifts macrophages toward a pro-inflammatory M1 phenotype, improving infection outcomes. Delivery via Tac-6 nanogel and adoptive transfer enables in vivo expression. Our method offers targeted, controllable treatment for CL, potentially overcoming current limitations. This platform also provides a versatile pipeline for studying macrophage-associated infections and inflammatory diseases, paving the way for precision immunotherapy. Impact statement We present a synthetic biology-based approach to treat cutaneous leishmaniasis by reprogramming macrophages with an inducible gene circuit expressing AI-designed peptides that boost IL-12 production and parasite clearance. Delivered via Tac-6 nanogel, this strategy offers targeted, resistance-mitigating therapy and a versatile platform for macrophage-driven diseases.