Towards precision antileishmanial drug discovery: Integrating multi-omics, functional genomics, artificial intelligence and host-directed therapeutics.

چکیده اصلی

Leishmaniasis remains one of the most neglected tropical diseases, affecting millions of people worldwide and posing a substantial public health burden in endemic regions. Current treatment options are limited by toxicity, high costs, prolonged treatment regimens, treatment failure, and the increasing emergence of drug-resistant parasites. Moreover, the remarkable genomic plasticity and adaptive capacity of Leishmania species, driven by mosaic aneuploidy and copy number variation, complicate durable target identification and underscore the need for precision-oriented therapeutic approaches. Recent developments in multi-omics strategies, CRISPR-based genome engineering, artificial intelligence, and host-directed therapeutics are transforming precision antileishmanial drug discovery. In this review, we explore how multi-omics technologies uncover pathways involved in parasite survival, virulence, and drug resistance. We examine the contributions of CRISPR-based technologies to functional genomic screening, target validation, and investigation of resistance mechanisms. Complementing these approaches, AI-assisted predictive modelling supports target prioritisation, virtual screening, and structure-guided drug discovery. We also discuss host-directed immunotherapy as a complementary strategy to parasite-directed therapies. Particular focus is placed on high-priority therapeutic pathways regulating redox homeostasis, sterol biosynthesis, MAP kinase signalling, mitochondrial electron transport, and arginine metabolism. Taken together, these strategies offer an integrated framework connecting target discovery, functional validation, computational prioritisation, and host immune modulation, while supporting a precision-oriented approach for the development of safer, more efficient, and resistance-resilient antileishmanial therapies.

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