Related Experiment Video
Updated: Jul 28, 2026

Experimental Human Pneumococcal Carriage
Published on: February 15, 2013
Low baseline antibody level to diphtheria is associated with poor response to conjugated pneumococcal vaccine in
M A Shelly1, M E Pichichero, J J Treanor
1Department of Medicine, Highland Hospital Rochester, New York, USA.
Insights
Low immunity to carrier proteins like diphtheria may explain why some older adults do not respond well to conjugated pneumococcal vaccines. This impacts the effectiveness of these important immunizations in the elderly population.
Area of Science:
- Immunology
- Vaccinology
- Geriatric Medicine
Background:
- Conjugating polysaccharide antigens to protein carriers enhances immunogenicity in infants.
- However, conjugated pneumococcal vaccines have shown disappointing results in older adults.
- Low pre-existing immunity to carrier proteins in the elderly may hinder T-cell-dependent responses.
Purpose of the Study:
- To investigate the impact of pre-existing immunity to carrier proteins on the immune response to pneumococcal vaccines in older adults.
- To compare immune responses between younger and older adults vaccinated with pneumococcal polysaccharide or conjugate vaccines.
Main Methods:
- Immunization of 49 older adults (60-78 years) and 50 younger adults (18-45 years) with pneumococcal polysaccharide vaccine or CRM197-conjugated pneumococcal oligosaccharide vaccine.
- Analysis of pre- and post-vaccination sera for antibodies to pneumococcal serotypes 14 and 6B, and diphtheria toxin using ELISA.
- Correlation of baseline diphtheria toxin antibody levels with post-vaccination antibody levels to pneumococcal antigens.
Main Results:
- Older adults had significantly lower baseline antibody levels to diphtheria toxin compared to younger adults.
- Higher baseline diphtheria toxin antibody levels correlated with increased post-vaccination antibody levels to pneumococcal serotype 6B.
- Antibody levels to pneumococcal serotype 14 showed a similar trend, particularly in the older adult group.
Conclusions:
- Low pre-existing immunity to diphtheria protein may contribute to diminished responses to conjugate pneumococcal vaccines in older adults.
- This finding suggests a potential mechanism for vaccine failure in the elderly and highlights the importance of carrier protein immunogenicity.
Abstract:
Joining polysaccharide antigens to protein increases immunogenicity in infants. In older adults, using conjugation to protein carriers to improve the immune response to pneumococcal polysaccharide vaccine has thus far proved disappointing. Low immunity to the carrier protein in the elderly may explain the failure of conjugated vaccines to elicit a T-cell-dependent response. We immunized 49 older adults (ages 60-78) and 50 younger adults (ages 18-45) with either 23-valent pneumococcal polysaccharide (PS) vaccine or 5-valent CRM197-conjugated pneumococcal oligosaccharide. Sera obtained before and after vaccination were analyzed for antibody to pneumococcal serotypes 14 and 6B and diphtheria toxin by ELISA. Baseline diphtheria toxin antibody level was lower in older adults than in younger adults (0.31 and 0.88 IU/ml, respectively; p < 0.0001). Adults with higher diphtheria antibody level had a higher antibody level to PS type 6B after vaccination than those with lower diphtheria antibody level (9.9 vs. 3.5 microg/ml, respectively; p = 0.01). Antibody level to PS type 14 was higher, but differed by baseline anti-diphtheria antibody level only when the older group was evaluated alone. Low levels of antibody to diphtheria protein may explain some of the lower responses to conjugate pneumococcal vaccine in older adults.
More Related Videos
Related Concept Videos
Humoral Immune Responses
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...
Development of Immunocompetence
The initial cells that migrate from the fetal thymus settle within the skin and epithelial tissues lining the mouth, digestive tract, and in females, the uterus and vagina. These cells, including skin-based dendritic cells, serve as antigen-presenting cells, playing a key role in T cell activation.
Subsequent T...
Pneumonia III: Complications and Assessment
Diphtheria

