1 Department of Human Anatomy, College of Medicine, Federal University Lokoja, Kogi State, Nigeria.
2 Department of Medical Laboratory Science, Ladoke Akintola University of Technology, Ogbomosho, Oyo, Nigeria.
3 Department of Microbiology, Kebbi State University of Science and Technology Aleiro, Nigeria.
4 Department of Biochemistry, African Centre of excellence of Mycotoxins and Food safety Research, Federal university of Technology, Minna, Nigeria.
5 Department of Microbiology, University of Nigeria, Nsukka.
6 Department of Basic Science and Research, Intercounty Centre for Oral Health for Africa, Jos, Nigeria.
7 Department of Anatomy, Ambrose Alli University, Ekpoma, Edo, Nigeria.
World Journal of Biology Pharmacy and Health Sciences, 2025, 22(02), 389–418
Article DOI: 10.30574/wjbphs.2025.22.2.0505
Received on 04 April 2025; revised on 20 May 2025; accepted on 22 May 2025
Infectious diseases remain a formidable global health burden, exacerbated by rising antimicrobial resistance, emerging viral outbreaks, and the persistent limitations of conventional therapeutic and diagnostic strategies. This review explores the revolutionary potential of gene editing technologies—most notably CRISPR-Cas systems, base editing, and prime editing—as transformative tools in the fight against infectious diseases. By elucidating the molecular mechanisms and precision capacities of these platforms, the article delineates how gene editing enables not only the direct eradication of viral and bacterial pathogens but also the modulation of host genetic responses to enhance immunity. Key applications include CRISPR-based excision of latent HIV reservoirs, base editing for hereditary viral susceptibility correction, and prime editing for monogenic disease interventions, all backed by compelling preclinical and early clinical evidence. Furthermore, the integration of gene editing with innovative delivery systems, such as engineered bacteriophages, lipid nanoparticles, and viral vectors, underscores its adaptability across both ex vivo and in vivo therapeutic landscapes. The review also illuminates CRISPR’s frontier role in developing next-generation diagnostics, offering unprecedented speed, specificity, and portability through platforms like SHERLOCK and DETECTR, especially vital in pandemic response and low-resource settings. Importantly, gene drives and synthetic biology applications in vector control—particularly against malaria and dengue—signal a paradigm shift in public health strategy, though accompanied by ethical, ecological, and regulatory complexities. Looking ahead, the synthesis of CRISPR with artificial intelligence, mRNA delivery platforms, and wearable diagnostics heralds a new era of personalized, programmable, and precision medicine. This article thus positions gene editing not merely as an ancillary tool but as a central pillar in the future architecture of infectious disease prevention, treatment, and global health resilience.
CRISPR Therapeutics; Gene Editing; Infectious Diseases; Antiviral Strategies; Synthetic Biology; Genetic Diagnostics; Bacterial Resistance; Genome Engineering.
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Fagbemi Oluwaseyi Ajibola, Toluwani Samuel Ogunmoyero, Mustapha Lawal, Iyiola Aanuoluwa Temitayo, Olonma Alexandra Nzei, Taiwo Emmanuel Olowodasa and Precious Airebanmen Otoibhili. Gene editing approaches to combat infectious diseases: Therapeutic innovations and diagnostic platforms. World Journal of Biology Pharmacy and Health Sciences, 2025, 22(02), 389–418. Article DOI: https://doi.org/10.30574/wjbphs.2025.22.2.0505.