Experimental evidence shows Lactobacillus enhances T-cell infiltration and reduces tumour volume, indicating a novel cytokine therapy approach.
Cancer accounts for over 10 million deaths annually, with solid tumours responsible for nearly 90% of cases worldwide. Systemic cytokine administration remains limited by severe toxicity, high-dose IL-2 therapy induces grade 3-4 adverse effects in >60% of patients, and treatment-related mortality is around 4%. In this context, engineered Lactobacillus strains designed to express tumour-killing cytokines such as IL-12, IL-15, and TRAIL represent a novel biotherapeutic strategy that combines microbial safety with precision immune activation. Experimental evidence shows that Lactobacillus plantarum secreting IL-12 reduces colorectal tumour volume by 65%, L. casei expressing TRAIL decreases pancreatic tumour mass by 40%, and L. reuteri producing IL-15 enhances CD8 + T-cell infiltration by 45% and improves survival by 30% in murine models. These data illustrate that cytokine-expressing probiotics can replicate the efficacy of systemic cytokine therapy while avoiding dose-limiting toxicity. Integrating synthetic biology tools such as inducible promoters and biosafety kill switches further refines control and containment, making this a viable candidate for translational development. The convergence of immunotherapy and microbiome engineering thus establishes engineered Lactobacillus as a novel, locally acting, and low-toxicity antitumour biotherapeutic with the potential to reshape next-generation cancer treatment.
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Mehmood et al. (2025) studied this question.
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