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Updated: Jan 22, 2026

Assessing Respiratory Immune Responses to Haemophilus Influenzae
Published on: June 29, 2021
A Cross-Reactive Protein Vaccine Combined with PCV-13 Prevents Streptococcus pneumoniae- and Haemophilus
Hannah M Rowe1, Beth Mann1, Amy Iverson1
1Department of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
Insights
A new protein-based vaccine offers protection against common childhood ear infections caused by Streptococcus pneumoniae and Haemophilus influenzae. This vaccine broadens immunity beyond current polysaccharide vaccines, enhancing protection for vaccinated and unvaccinated strains.
Area of Science:
- Microbiology and Immunology
- Vaccine Development
- Pediatric Infectious Diseases
Background:
- Acute otitis media (AOM) is a widespread childhood infection globally.
- Current vaccines against Streptococcus pneumoniae target capsular polysaccharides, leaving gaps in protection against non-encapsulated strains and un-covered serotypes.
- Mucosal infections like AOM persist despite existing vaccination strategies.
Purpose of the Study:
- To evaluate a novel protein-based vaccine for its efficacy against pneumococcal AOM.
- To assess the vaccine's protective effects against non-vaccine serotypes and its synergistic potential with existing vaccines.
- To determine the vaccine's ability to confer cross-protection against other otopathogens, including nontypeable Haemophilus influenzae.
Main Methods:
- Development of a fusion protein vaccine combining epitopes of CbpA with pneumolysin toxoid.
- Assessment of vaccine efficacy in protection models against pneumococcal AOM.
- Evaluation of antibody responses and cross-reactivity against multiple otopathogens.
Main Results:
- The protein-based vaccine demonstrated effective protection against pneumococcal AOM for non-PCV-13 serotypes.
- Co-administration with PCV-13 enhanced protection for PCV-13 serotypes.
- The fusion protein induced potent antibody responses against nontypeable Haemophilus influenzae and Streptococcus pneumoniae, providing protection against unencapsulated strains.
Conclusions:
- Augmenting current capsule-based vaccination with conserved, cross-reactive protein-based vaccines can broaden and enhance protection against AOM.
- This strategy offers a promising approach to combat prevalent childhood ear infections caused by diverse bacterial pathogens.
- The developed fusion protein vaccine shows potential for improved AOM prevention in children.
Abstract:
Acute otitis media is one of the most common childhood infections worldwide. Currently licensed vaccines against the common otopathogen Streptococcus pneumoniae target the bacterial capsular polysaccharide and confer no protection against nonencapsulated strains or capsular types outside vaccine coverage. Mucosal infections such as acute otitis media remain prevalent, even those caused by vaccine-covered serotypes. Here, we report that a protein-based vaccine, a fusion construct of epitopes of CbpA to pneumolysin toxoid, confers effective protection against pneumococcal acute otitis media for non-PCV-13 serotypes and enhances protection for PCV-13 serotypes when coadministered with PCV-13. Having cross-reactive epitopes, the fusion protein also induces potent antibody responses against nontypeable Haemophilus influenzae and S. pneumoniae, engendering protection against acute otitis media caused by emerging unencapsulated otopathogens. These data suggest that augmenting capsule-based vaccination with conserved, cross-reactive protein-based vaccines broadens and enhances protection against acute otitis media.
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