MV140 Mucosal Vaccine Induces Targeted Immune Response for Enhanced Clearance of Uropathogenic E. coli in Experimental Urinary Tract Infection.
Paula Saz-LealMarianne Morris LigonCarmen María Diez-RiveroDiego García-AyusoSoumitra MohantyMarcos ViñuelaIrene Real-ArévaloLaura ConejeroAnnelie BraunerJosé Luis SubizaIndira Uppugunduri MysorekarPublished in: Vaccines (2024)
MV140 is an inactivated whole-cell bacterial mucosal vaccine with proven clinical efficacy against recurrent urinary tract infections (UTIs). These infections are primarily caused by uropathogenic E. coli (UPEC) strains, which are unique in their virulence factors and remarkably diverse. MV140 contains a non-UPEC strain, suggesting that it may induce an immune response against different UPEC-induced UTIs in patients. To verify this, we experimentally evaluated the cellular and humoral responses to UTI89, a prototypical UPEC strain, in mice vaccinated with MV140, as well as the degree of protection achieved in a UPEC UTI89 model of acute cystitis. The results show that both cellular (Th1/Th17) and antibody (IgG/IgA) responses to UTI89 were induced in MV140-immunized mice. MV140 vaccination resulted in an early increased clearance of UTI89 viable bacteria in the bladder and urine following transurethral infection. This was accompanied by a highly significant increase in CD4 + T cells in the bladder and an increase in urinary neutrophils. Collectively, our results support that MV140 induces cross-reactive humoral and cellular immune responses and cross-protection against UPEC strains.
Keyphrases
- urinary tract infection
- immune response
- escherichia coli
- dendritic cells
- high glucose
- toll like receptor
- biofilm formation
- end stage renal disease
- diabetic rats
- liver failure
- high fat diet induced
- mesenchymal stem cells
- ejection fraction
- single cell
- stem cells
- oxidative stress
- cell therapy
- newly diagnosed
- hepatitis b virus
- metabolic syndrome
- antimicrobial resistance
- insulin resistance
- peritoneal dialysis
- ulcerative colitis
- adipose tissue
- intensive care unit
- respiratory failure
- drug delivery
- endothelial cells
- extracorporeal membrane oxygenation