Drug intelligence / Profile preview

salmonella typhimurium A1-R

Development stage
Preclinical
Lead developer
AntiCancer
Modality
Synthetic Biology Platforms → Engineered Microbial Therapeutics → Microbiome Therapeutics, Fresh FMT → Fecal Microbiota Transplantation (FMT) → Microbiome Therapeutics, Yeast Strains → Single Strain Products → Live Biotherapeutic Products → Microbiome Therapeutics, Bacterial Strains → Single Strain Products → Live Biotherapeutic Products → Microbiome Therapeutics, Defined Consortia → Multi-strain Products → Live Biotherapeutic Products → Microbiome Therapeutics, Frozen FMT → Fecal Microbiota Transplantation (FMT) → Microbiome Therapeutics, Genetically Modified Bacteria → Engineered Microbial Therapeutics → Microbiome Therapeutics, Microbial Metabolites → Microbiome-Derived Products → Microbiome Therapeutics, Microbial Proteins → Microbiome-Derived Products → Microbiome Therapeutics, Complex Communities → Multi-strain Products → Live Biotherapeutic Products → Microbiome Therapeutics
Administration
Intratumoral, Intravenous, Intraperitoneal
01

Overview

Salmonella typhimurium A1-R is a genetically modified, tumor-targeting strain of *Salmonella enterica* serovar Typhimurium. Engineered to be auxotrophic for leucine and arginine, it preferentially proliferates in tumor microenvironments, where these amino acids are available, while sparing normal tissues[1][4][6]. The bacterium directly kills cancer cells by infecting, replicating within, and lysing tumor cells; it also induces central tumor necrosis via growth in hypoxic/anaerobic conditions[1][4]. In preclinical models, A1-R has demonstrated efficacy against a wide range of recalcitrant cancers, including melanoma, glioma, breast, pancreatic, colon, prostate, ovarian, cervical, lung cancer, osteosarcoma, and fibrosarcoma[1][2][4][6]. It has also been shown to synergize with chemotherapeutic and molecular-targeted agents. Mechanistically, it triggers both innate and adaptive antitumor immune responses through activation of cytokines (e.g., interferon-γ) and recruitment of immune cells via Toll-like receptor 4 signaling[1]. The strain was primarily developed and characterized by AntiCancer and academic collaborators[4][5].

02

Targets

TLR4 (Toll-like receptor 4)

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