Pneumococcal vaccine significantly reduces disease in South African children

October 01, 2003

ATLANTA--In a clinical trial conducted in nearly 40,000 young children in Soweto, South Africa, a pneumococcal conjugate vaccine aimed at nine strains of disease reduced the incidence of pneumonia in fully vaccinated children by 25 percent. In addition, the vaccine reduced the incidence of invasive pneumococcal disease (pneumococcal bacteria in the bloodstream) by more than 83 percent in non-HIV-infected children and by more than 65 percent in HIV-infected children. The vaccine also significantly reduced the incidence of invasive pneumococcal disease caused by antibiotic-resistant strains by between 56 and 67 percent, depending on the type of resistance.

The study took place between 1998 and 2000, with follow-up through 2001. The results are published in the October 2 issue of The New England Journal of Medicine.

Participating institutions included Emory University, the University of the Witwatersrand in South Africa, Johns Hopkins University and Wyeth Pharmaceuticals, under the auspices of the World Health Organization (WHO) and the Medical Research Council of South Africa. Keith P. Klugman, MD, professor of international health in Emory University's Rollins School of Public Health and professor of medicine in Emory University School of Medicine, was principal investigator of the study.

The clinical trial randomized two groups of infants to receive either three doses of the conjugate vaccine or placebo. In addition, all children received Haemophilus influenzae type b (Hib) conjugate vaccine. The scientists tracked the conjugate vaccine's effectiveness over a four-year period through active surveillance of children with pneumococcal disease at the large academic hospital serving the community of Soweto. Antibiotic-resistant strains of pneumococci are common in Soweto, and HIV infection is the leading risk factor for invasive pneumococcal disease. The overall mortality rate in the clinical trial was reduced by five percent among all children and by six percent among HIV-infected children.

According to the WHO, pneumonia is the leading cause of death in children worldwide and is responsible for approximately four million deaths a year. Most of these deaths occur in developing countries. Streptococcuus pneumoniae, the primary bacterial pathogen leading to pneumonia, has become increasingly resistant to antibiotics.

A vaccine is now indicated for all U.S. children to prevent invasive pneumococcal disease and bacterial meningitis, and is administered in infancy. The vaccine targets seven strains of pneumococcal disease, while the vaccine used in the South African clinical trial targets two additional strains of pneumococcus that are prevalent in developing countries. The 9-valent conjugate vaccine is currently under development for both developed and developing countries, but has not yet been licensed for use.

"With this reduction in the incidence of pneumonia in the developing world, we could potentially save over 500,000 lives each year," said Dr. Klugman. "In addition, no vaccine has previously been documented to prevent pneumococcal disease in HIV-infected children, and our study showed a 50 percent reduction in that group. In an era in which there is little to offer to children with HIV, we can clearly reduce invasive disease by providing this vaccine to all children. Our study provides evidence to support the use of this vaccine to prevent invasive pneumococcal disease, reduce antibiotic resistance and diminish the incidence of pneumonia in children"
-end-


Emory University Health Sciences Center

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