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Efficacy of Haemophilus influenzae type b polysaccharide-diphtheria toxoid conjugate vaccine in infancy
Insights
The Haemophilus influenzae type b conjugate vaccine effectively protects infants. This vaccine demonstrated an 83% reduction in invasive H. influenzae infections in a large Finnish trial.
Area of Science:
- Immunology
- Pediatrics
- Vaccinology
Background:
- Haemophilus influenzae type b (Hib) infections pose a significant threat to infant health.
- Developing effective vaccines for infants is crucial for disease prevention.
Purpose of the Study:
- To evaluate the clinical efficacy of the Haemophilus influenzae type b capsular polysaccharide-diphtheria toxoid conjugate vaccine in infants.
- To assess the immunogenicity and safety profile of the Hib conjugate vaccine.
Main Methods:
- An open trial involving 60,000 children in Finland.
- Vaccine administered at 3, 4, 6, and 14 months to infants born on odd-numbered days; even-numbered day births served as controls.
- Antibody titers measured in a cohort of 99 infants; invasive Hib infections tracked.
Main Results:
- Geometric mean antibody titer increased from 0.08 to 0.42 microgram/mL between 3 and 7 months of age.
- Only minor adverse reactions were reported, indicating a favorable safety profile.
- A significant reduction in invasive Hib infections: 2 cases in the vaccinated group versus 12 in the control group (P = 0.0005).
Conclusions:
- The Hib conjugate vaccine is highly effective in preventing invasive H. influenzae infections in infants.
- The vaccine demonstrates robust immunogenicity and a good safety profile in young children.
- This conjugate vaccine provides substantial short-term protection against Hib disease during infancy.
Abstract:
Haemophilus influenzae type b capsular polysaccharide-diphtheria toxoid conjugate vaccine has recently been shown to be capable of inducing antibodies to H. influenzae in infants. In an evaluation of its clinical efficacy, 60,000 children were enrolled in an open trial in Finland. Children born on odd-numbered days between October 1, 1985, and September 30, 1986, received the vaccine at 3, 4, 6, and 14 months; those born on even-numbered days served as controls. The geometric mean antibody titer measured in a cohort of 99 children rose from a prevaccination level of 0.08 microgram per milliliter at three months of age to 0.42 microgram per milliliter at seven months. Only minor adverse reactions were reported. Up to February 1987, two cases of invasive H. influenzae infection had occurred among the children who had received three doses of vaccine, whereas 12 cases had occurred among the controls (P = 0.0005 by Poisson one-tailed test). The rate of short-term (average follow-up time, five months) protection provided by this conjugate vaccine in infancy was thus 83 percent.
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