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Updated: Apr 30, 2026

Experimental Human Pneumococcal Carriage
Published on: February 15, 2013
The CAPITA study of protein-conjugate pneumococcal vaccine and its implications for use in adults in developed
Daniel M Musher1, Maria C Rodriguez-Barradas1
1From the Medical Service (Infectious Disease Section); Michael E. DeBakey Veterans Affairs Medical Center; Houston, TX USA; Department of Medicine; Baylor College of Medicine; Houston, TX USA; Department of Molecular Virology and Microbiology; Baylor College of Medicine; Houston, TX USA.
Insights
A new vaccine strategy using Hemophilus influenzae type b (HITB) polysaccharide conjugated to protein dramatically improved antibody response in infants. This breakthrough nearly eradicated HITB infections in young children in the United States.
Area of Science:
- Pediatric infectious diseases
- Vaccine development
- Immunology
Background:
- Until 1990, Hemophilus influenzae type b (HITB) was a significant cause of childhood illness and death.
- The initial HITB vaccine, using purified capsular polysaccharide (PRP), was ineffective in infants and toddlers and subsequently withdrawn.
Purpose of the Study:
- To investigate the efficacy of a novel vaccine approach for preventing HITB infections in young children.
- To understand the immunological basis for improved vaccine response.
Main Methods:
- Development of a conjugate vaccine by covalently linking PRP to an antigenic protein.
- Administration of the conjugate vaccine to infants and toddlers to assess immunogenicity.
Main Results:
- The conjugate vaccine elicited a robust antibody response in infants and toddlers, unlike the unconjugated polysaccharide vaccine.
- The widespread use of the conjugate vaccine has led to a dramatic reduction in HITB infections.
Conclusions:
- Conjugating PRP to a protein carrier is a highly effective strategy for inducing protective immunity against HITB in young children.
- This vaccine development has been instrumental in nearly eradicating HITB disease in the United States.
Abstract:
Until 1990, Hemophilus influenzae type b (HITB) was a major cause of morbidity and mortality in toddlers and young children. A vaccine consisting of purified polyribosyl ribitol phosphate (PRP), the capsular polysaccharide (CPS) of HITB, had been shown to be ineffective as an antigen in the population at risk, and this vaccine was withdrawn from the market within a few years of its introduction. By contrast, the discovery that PRP, when covalently bound to an antigenic protein, stimulated antibody production in infants and toddlers, (1) led to the development of a vaccine that has all but eradicated HITB infection and brought about a near-disappearance of this organism in the United States.
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