Immunity to Chlamydia pneumoniae induced by vaccination with DNA vectors expressing a cytoplasmic protein (Hsp60) or outer membrane proteins (MOMP and Omp2)
Related Experiment Video
Updated: Oct 10, 2026

Cell-Free Scaled Production and Adjuvant Addition to a Recombinant Major Outer Membrane Protein from Chlamydia muridarum for Vaccine Development
Published on: March 16, 2022
T Penttilä1, J M Vuola, V Puurula
1Department of Virology, POB 21, Haartman Institute, University of Helsinki, FIN-00014, Helsinki, Finland. tulla.penttila@helsinki.fi
Abstract:
Immune responses induced by intramuscular DNA immunization with Chlamydia pneumoniae genes coding for the major outer membrane protein (MOMP), cysteine-rich outer membrane protein 2 (Omp2) or the heat shock protein 60 (Hsp60) were studied. BALB/c mice were vaccinated intramuscularly three times at 3-week intervals and challenged intranasally 2 weeks after the last injection. Immunization with pmomp or phsp60 showed 1.2-1.5 log reduction in the mean lung bacterial counts after the challenge. Specific antibodies were detected only in sera of the mice immunized with pomp2 and phsp60. Although immunization with pomp2 resulted in a strong serum antibody response against Omp2 protein, it failed to protect the mice. Immunization with any of the three vaccines did not reduce the severity of histologically assessed pneumonia, but resulted in significantly higher lymphoid reaction in the lung indicating immunological memory.
Insights
DNA vaccines targeting Chlamydia pneumoniae outer membrane protein (MOMP) or heat shock protein 60 (Hsp60) reduced lung bacterial counts in mice. However, none of the vaccines prevented pneumonia, despite inducing immunological memory.
Area of Science:
- * Molecular biology and immunology
- * Infectious disease research
Background:
- * Chlamydia pneumoniae is a significant respiratory pathogen.
- * Developing effective vaccines against C. pneumoniae is crucial for public health.
Purpose of the Study:
- * To evaluate the immunogenicity and protective efficacy of DNA vaccines encoding C. pneumoniae MOMP, Omp2, and Hsp60.
- * To assess the impact of these vaccines on bacterial load, antibody response, and lung pathology.
Main Methods:
- * BALB/c mice were intramuscularly vaccinated three times with DNA plasmids encoding MOMP, Omp2, or Hsp60.
- * Mice were challenged intranasally with C. pneumoniae.
- * Lung bacterial counts, serum antibody levels, and histological lung sections were analyzed.
Main Results:
- * Vaccination with MOMP or Hsp60 DNA vaccines resulted in a 1.2-1.5 log reduction in lung bacterial counts.
- * Specific antibodies were detected in mice vaccinated with Omp2 or Hsp60 DNA vaccines.
- * No vaccine significantly reduced the severity of pneumonia, but all induced higher lymphoid reactions in the lungs.
Conclusions:
- * DNA vaccines encoding C. pneumoniae MOMP and Hsp60 demonstrate partial efficacy in reducing bacterial load.
- * While antibody responses were observed, complete protection against infection and pneumonia was not achieved.
- * The vaccines induced immunological memory in the lungs, suggesting potential for future vaccine development.
Related Concept Videos
Vaccinations
Immunological Memory
What is Immunological Memory?
Immunological memory is an integral function of the immune system that allows it to recognize and react more rapidly and effectively to pathogens previously encountered. This feature is...
Vaccines
Active versus Passive Immunity
Active Immunity
Active immunity refers to the resistance one develops...

