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Updated: Feb 15, 2026

Mouse Models Of Helicobacter Infection And Gastric Pathologies
Published on: October 18, 2018
Immunization with recombinant FliD confers protection against Helicobacter pylori infection in mice
Amir Ghasemi1, Nazanin Mohammad2, Josef Mautner3
1Department of Microbiology and Immunology, Faculty of Medicine, Kashan University of Medical Sciences, Kashan, Iran; Department of Infectious Disease and Immunology, College of Veterinary Medicine, University of Florida, FL, USA.
Abstract:
Nearly half of the world's population is infected with Helicobacter pylori. Clinical manifestations of this infection range from gastritis and peptic ulcers to gastric adenocarcinoma and lymphoma. Due to the emerging of antibiotic resistant strains and poor patient compliance of the antibiotic therapy, there is increasing interest in the development of a protective vaccine against H. pylori infection. The bacterial protein FliD forms a capping structure on the end of each flagellum which is critical to prevent depolymerization and structural degradation. In this study, the potential of FliD as a prospective H. pylori subunit vaccine was assessed. For this purpose, immunogenicity and protective efficacy of recombinant FliD (rFliD) from H. pylori was evaluated in C57BL/6 mice. Purified rFliD was formulated with different adjuvants and administered via subcutaneous or oral route. Subcutaneous immunization with rFliD elicited predominantly mixed Th1 and Th17 immune responses, with high titers of specific IgG1 and IgG2a. Splenocytes of immunized mice exhibited strong antigen-specific memory responses, resulting in the secretion of high amounts of IFN-γ and IL-17, and low levels of IL-4. Immunization with rFliD caused a significant reduction in H. pylori bacterial load relative to naïve control mice (p < 0.001), demonstrating a robust protective effect. Taken together, these results suggest that subcutaneous vaccination with rFliD formulated with CpG or Addavax could be considered as a potential candidate for the development of a subunit vaccine against H. pylori infection.
Insights
A new Helicobacter pylori vaccine candidate using the bacterial protein FliD shows promise. Subcutaneous vaccination with recombinant FliD (rFliD) in mice significantly reduced bacterial load, indicating a potential protective effect against H. pylori infection.
Area of Science:
- Microbiology
- Immunology
- Vaccinology
Background:
- Helicobacter pylori infection affects nearly half the global population, leading to various gastrointestinal diseases.
- Antibiotic resistance and poor patient compliance necessitate alternative strategies like vaccines.
- The bacterial flagellar protein FliD is crucial for flagellar structure and stability.
Purpose of the Study:
- To evaluate the immunogenicity and protective efficacy of recombinant FliD (rFliD) from H. pylori as a subunit vaccine candidate.
- To assess the immune responses induced by subcutaneous and oral administration of rFliD with different adjuvants in mice.
Main Methods:
- Recombinant FliD (rFliD) was purified and formulated with adjuvants.
- C57BL/6 mice were immunized subcutaneously or orally with rFliD.
- Humoral and cellular immune responses (IgG titers, cytokine secretion) were analyzed.
- Bacterial load of H. pylori was measured post-challenge to assess protective efficacy.
Main Results:
- Subcutaneous immunization with rFliD induced strong Th1 and Th17 immune responses, characterized by high IgG1, IgG2a titers, and elevated IFN-γ and IL-17 secretion.
- Splenocytes from immunized mice showed robust antigen-specific memory responses.
- Immunization with rFliD led to a significant reduction in H. pylori bacterial load compared to controls (p < 0.001).
Conclusions:
- Subcutaneous vaccination with rFliD, particularly when formulated with CpG or Addavax, demonstrates significant protective efficacy against H. pylori infection in a mouse model.
- rFliD is a promising candidate for developing a novel subunit vaccine against H. pylori.
- The study highlights the potential of targeting bacterial structural proteins for vaccine development.
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