Membrane Vesicles from Lacticaseibacillus Casei BL23 Exhibit Antimicrobial Activity Against Escherichia coli and Immunostimulatory Effects on Human Peripheral Blood Mononuclear Cells

Adv Healthc Mater. 2026 Apr;15(16):e00548. doi: 10.1002/adhm.202500548. Epub 2025 Dec 5.

Abstract

Probiotics are live microorganisms known for their health benefits; however, they may pose risks for immunocompromised individuals. This study explores the potential of postbiotics, specifically membrane vesicles (MVs) derived from Lacticaseibacillus casei BL23, as a safer alternative. MVs are isolated via ultracentrifugation (UC) followed by size exclusion chromatography (SEC), revealing a mean size of 178 nm and a concentration of 2.53×1011 particles mL-1, with moderate stability over four months at 4°C. Antimicrobial assays demonstrate that SEC-isolated MVs effectively inhibit the growth of Escherichia coli DH5α. Confocal laser scanning microscopy confirms the internalization of MVs by both E. coli and macrophages. Additionally, MV treatment elicits a significant immune response, marked by increased levels of pro-inflammatory cytokines (TNF-α, IL-6, IL-8, IL-1β) alongside IL-10 production in peripheral blood mononuclear cells. Importantly, cytotoxicity assays indicate that MVs are non-toxic to these cells and preserve epithelial barrier integrity in Caco-2 cell monolayers. MVs showed a trend towards extending lifespan in the Caenorhabditis elegans in vivo model upon infection with Pseudomonas aeruginosa. These findings underscore the dual-activity potential of L. casei BL23 MVs as effective tools for combating infections while enhancing immune function, offering a promising strategy to address antibiotic resistance.

Keywords: antimicrobial activity; immune response; membrane vesicles; probiotics.

MeSH terms

  • Animals
  • Caco-2 Cells
  • Caenorhabditis elegans / microbiology
  • Cytokines / metabolism
  • Escherichia coli* / drug effects
  • Humans
  • Lacticaseibacillus casei* / chemistry
  • Lacticaseibacillus casei* / metabolism
  • Leukocytes, Mononuclear* / drug effects
  • Leukocytes, Mononuclear* / immunology
  • Leukocytes, Mononuclear* / metabolism

Substances

  • Cytokines