Drug intelligence / Profile preview

lactobacillus fermentum TSF331

Development stage
Unknown
Lead developer
Glac Biotech
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
Oral
01

Overview

**Lactobacillus fermentum TSF331** is a probiotic bacterial strain developed for potential therapeutic use in metabolic disorders. The strain has been studied for its ability to assimilate purine nucleosides, particularly inosine and guanosine, which leads to a reduction in serum uric acid (UA) levels. In animal models of hyperuricemia, TSF331 decreased serum UA by approximately 30% and demonstrated strong in vitro purine assimilation properties. Clinical studies in humans have also shown that supplementation with TSF331, alone or in combination with other probiotic strains, significantly improves liver function markers (AST, ALT) and lowers serum UA levels, and promotes healthier gut microbiota composition. The mechanism of action includes the metabolism of purine derivatives, potentially leading to reduced substrate for uric acid production and enhanced uric acid excretion. TSF331 is currently being investigated as a dietary probiotic intervention for metabolic-associated fatty liver disease (MAFLD) and hyperuricemia. No significant adverse effects have been reported in preclinical or early clinical studies[1][2][3][4][5].

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