Continued Impact of Pneumococcal Conjugate Vaccine on Carriage in Young Children

Author:

Huang Susan S.12,Hinrichsen Virginia L.3,Stevenson Abbie E.4,Rifas-Shiman Sheryl L.3,Kleinman Ken3,Pelton Stephen I.4,Lipsitch Marc56,Hanage William P.7,Lee Grace M.3,Finkelstein Jonathan A.389

Affiliation:

1. Division of Infectious Diseases, University of California, Irvine School of Medicine, Irvine, California

2. Channing Laboratory, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts

3. Department of Ambulatory Care and Prevention, Harvard Medical School and Harvard Pilgrim Health Care, Boston, Massachusetts

4. Department of Pediatrics, Boston University School of Medicine, Boston, Massachusetts

5. Departments of Epidemiology

6. Immunology and Infectious Diseases, Harvard School of Public Health, Boston, Massachusetts

7. Department of Infectious Disease Epidemiology, Imperial College, London, England

8. Department of Pediatrics, Harvard Medical School, Boston, Massachusetts

9. Division of General Pediatrics, Children's Hospital Boston, Boston, Massachusetts

Abstract

OBJECTIVES: The goals were to assess serial changes in Streptococcus pneumoniae serotypes and antibiotic resistance in young children and to evaluate whether risk factors for carriage have been altered by heptavalent pneumococcal conjugate vaccine (PCV7). METHODS: Nasopharyngeal specimens and questionnaire/medical record data were obtained from children 3 months to <7 years of age in primary care practices in 16 Massachusetts communities during the winter seasons of 2000–2001 and 2003–2004 and in 8 communities in 2006–2007. Antimicrobial susceptibility testing and serotyping were performed with S pneumoniae isolates. RESULTS: We collected 678, 988, and 972 specimens during the sampling periods in 2000–2001, 2003–2004, and 2006–2007, respectively. Carriage of non-PCV7 serotypes increased from 15% to 19% and 29% (P < .001), with vaccine serotypes decreasing to 3% of carried serotypes in 2006–2007. The relative contribution of several non-PCV7 serotypes, including 19A, 35B, and 23A, increased across sampling periods. By 2007, commonly carried serotypes included 19A (16%), 6A (12%), 15B/C (11%), 35B (9%), and 11A (8%), and high-prevalence serotypes seemed to have greater proportions of penicillin nonsusceptibility. In multivariate models, common predictors of pneumococcal carriage, such as child care attendance, upper respiratory tract infection, and the presence of young siblings, persisted. CONCLUSIONS: The virtual disappearance of vaccine serotypes in S pneumoniae carriage has occurred in young children, with rapid replacement with penicillin-nonsusceptible nonvaccine serotypes, particularly 19A and 35B. Except for the age group at highest risk, previous predictors of carriage, such as child care attendance and the presence of young siblings, have not been changed by the vaccine.

Publisher

American Academy of Pediatrics (AAP)

Subject

Pediatrics, Perinatology, and Child Health

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