Drug intelligence / Profile preview

LGG-bEVs

Development stage
Preclinical
Lead developer
University of Cincinnati
Modality
Defined Consortia → Multi-strain Products → Live Biotherapeutic Products → Microbiome Therapeutics, Microbial Metabolites → Microbiome-Derived Products → Microbiome Therapeutics, Lipid-based Nanoparticles → Nanoparticles → Drug Delivery Systems, Synthetic Biology Platforms → Engineered Microbial Therapeutics → Microbiome Therapeutics, Fresh FMT → Fecal Microbiota Transplantation (FMT) → Microbiome Therapeutics, Genetically Modified Bacteria → Engineered Microbial Therapeutics → Microbiome Therapeutics, Yeast Strains → Single Strain Products → Live Biotherapeutic Products → Microbiome Therapeutics, Frozen FMT → Fecal Microbiota Transplantation (FMT) → Microbiome Therapeutics, Bacterial Strains → Single Strain Products → Live Biotherapeutic Products → Microbiome Therapeutics, Microbial Proteins → Microbiome-Derived Products → Microbiome Therapeutics, RNA Therapeutics → Nucleic Acid Therapeutics, Complex Communities → Multi-strain Products → Live Biotherapeutic Products → Microbiome Therapeutics
Administration
Intravenous
01

Overview

LGG-bEVs are extracellular vesicles derived from the probiotic bacterium Lactobacillus rhamnosus GG (LGG). These bacterial extracellular vesicles (bEVs) function as therapeutic agents by delivering specific cargo, notably 5s-rRNA-derived short RNA fragments, to macrophages. In the context of myocardial ischemia/reperfusion (I/R) injury, LGG-bEVs stimulate macrophage efferocytosis—the process of clearing dead cardiomyocytes—thereby limiting sterile inflammation and cardiac remodeling. Mechanistically, the RNA cargo interacts with the coding regions of genes such as DDX5, YWHAZ, and FRMD4A, upregulating their expression to enhance phagocytic activity. Research conducted by institutions like the University of Cincinnati has demonstrated that systemic administration of LGG-bEVs in mouse models reduces inflammatory cytokine levels (IL-6, TNF-α, MCP-1) and improves long-term cardiac function post-infarction.

Other names
Lactobacillus rhamnosus GG-derived extracellular vesiclesprobiotic extracellular vesicles from LGG
02

Targets

DDX5 (Phosphorylated-p68 RNA helicase)FRMD4A (FERM domain-containing protein 4A)YWHA (14-3-3 protein family)

Beyond the preview

Go deeper on LGG-bEVs.

Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.

Clinical trials

Full profile access

Follow clinical development from study design and recruitment through results.

  • Trial phase
  • Status
  • Readouts

Indications & development

Full profile access

Explore development by indication, patient population, and geography.

  • Indications
  • Development status
  • Countries

Licensing & deals

Full profile access

Trace asset ownership, licensing agreements, and commercial partnerships.

  • Partners
  • Deal terms
  • Milestones

Patents & exclusivity

Full profile access

Explore the patent landscape and regulatory exclusivity around an asset.

  • Patents
  • Expiration dates
  • Exclusivity

Competitive landscape

Full profile access

Compare development programs by target, modality, and indication.

  • Competing assets
  • Targets
  • Development stage

Research & analysis

Full profile access

Connect source evidence and development news to your research questions.

  • Publications
  • News
  • Analysis

Bring the full picture into focus.

See how Gosset can support your research on LGG-bEVs.

Explore the full profile

Gosset Free

Get started with Gosset.

Enter your work email and we’ll be in touch with next steps.

Work email preferred.

Book a call