POTENTIAL INTERVENTIONS FOR THE PREVENTION OF CHILDHOOD PNEUMONIA - GEOGRAPHIC AND TEMPORAL DIFFERENCES IN SEROTYPE AND SEROGROUP DISTRIBUTION OF STERILE SITE PNEUMOCOCCAL ISOLATES FROM CHILDREN - IMPLICATIONSFOR VACCINE STRATEGIES
Dh. Sniadack et al., POTENTIAL INTERVENTIONS FOR THE PREVENTION OF CHILDHOOD PNEUMONIA - GEOGRAPHIC AND TEMPORAL DIFFERENCES IN SEROTYPE AND SEROGROUP DISTRIBUTION OF STERILE SITE PNEUMOCOCCAL ISOLATES FROM CHILDREN - IMPLICATIONSFOR VACCINE STRATEGIES, The Pediatric infectious disease journal, 14(6), 1995, pp. 503-510
Streptococcus pneumoniae is a leading cause of fatal bacterial pneumon
ia in young children. Pneumococcal polysaccharide vaccines have not be
en promoted for use in young children because many constituent serotyp
es are not immunogenic in children < 2 years old. Conjugating pneumoco
ccal polysaccharide epitopes to a protein carrier would likely increas
e vaccine immunogenicity in children, We reviewed published and unpubl
ished pneumococcal serotype and serogroup data from 16 countries on 6
continents to determine geographic and temporal differences in serotyp
e and serogroup distribution of sterile site pneumococcal isolates amo
ng children and to estimate coverage of proposed and potential pneumoc
occal conjugate vaccine formulas, The most common pneumococcal serotyp
es or groups from developed countries were, in descending order, 14, 6
, 19, 18, 9, 23, 7, 4, 1 and 15. In developing countries the order was
6, 14, 8, 5, 1, 19, 9, 23, 18, 15 and 7. Development of customized he
ptavalent vaccine formulas, one for use in all developed countries and
one for use in all developing countries, would not provide substantia
lly better coverage against invasive pneumococcal disease than two cur
rently proposed heptavalent formulas, An optimal nanovalent vaccine fo
r global use would include serotypes 1, 5, 6B, 7F, 9V, 14, 18C, 19F an
d 23F. Geographic and temporal variation in pneumococcal serotypes dem
onstrates the need for a species-wide pneumococcal vaccine.