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Immunogenicity and safety of 13-valent pneumococcal conjugate vaccine in infants and toddlers.
Pediatrics. 2010 Sep; 126(3):e493-505.Ped

Abstract

BACKGROUND

7-Valent pneumococcal conjugate vaccine (PCV7 [Prevnar, Wyeth Pharmaceuticals Inc, Philadelphia, PA], serotypes 4, 6B, 9V, 14, 18C, 19F, and 23F) is effective in preventing vaccine-serotype pneumococcal disease. 13-Valent pneumococcal conjugate vaccine (PCV13) (PCV7 serotypes plus 1, 3, 5, 6A, 7F, and 19A) was designed to provide broader pneumococcal disease coverage. We evaluated the immunogenicity and safety of PCV13 compared with PCV7.

METHODS

Infants received PCV13 or PCV7 at ages 2, 4, 6, and 12 to 15 months with routine pediatric vaccinations. Pneumococcal anticapsular polysaccharide-binding immunoglobulin G responses and functional antipneumococcal opsonophagocytic activity were assessed 1 month after dose 3, before the toddler dose, and 1 month after the toddler dose. Safety and tolerability were also assessed.

RESULTS

For the 7 common serotypes, PCV13-elicited immunoglobulin G titers were noninferior to those elicited by PCV7, although PCV13 responses were generally somewhat lower. PCV13 also elicited functional opsonophagocytic activity comparable with that elicited by PCV7. For the 6 additional serotypes in PCV13, PCV13 elicited binding and functional antibody levels notably greater than those in PCV7 recipients. After PCV13 immunization, concordance between antipolysaccharide and opsonophagocytic responses was noted for all 13 serotypes. The PCV13 toddler dose resulted in higher immune responses compared with infant-series doses. Safety and tolerability were comparable; reactogenicity was generally mild.

CONCLUSIONS

PCV13 will be as effective as PCV7 in the prevention of pneumococcal disease caused by the 7 common serotypes and could provide expanded protection against the 6 additional serotypes. The PCV13 safety profile was comparable to that of PCV7.

Authors+Show Affiliations

Vaccine Research Center, Los Angeles Biomedical Research Institute, Harbor-UCLA Medical Center, 1124 West Carson St, Liu Research Building, Torrance, CA 90502, USA. syeh@uclacvr.labiomed.orgNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Clinical Trial, Phase III
Comparative Study
Journal Article
Multicenter Study
Randomized Controlled Trial
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

20732948

Citation

Yeh, Sylvia H., et al. "Immunogenicity and Safety of 13-valent Pneumococcal Conjugate Vaccine in Infants and Toddlers." Pediatrics, vol. 126, no. 3, 2010, pp. e493-505.
Yeh SH, Gurtman A, Hurley DC, et al. Immunogenicity and safety of 13-valent pneumococcal conjugate vaccine in infants and toddlers. Pediatrics. 2010;126(3):e493-505.
Yeh, S. H., Gurtman, A., Hurley, D. C., Block, S. L., Schwartz, R. H., Patterson, S., Jansen, K. U., Love, J., Gruber, W. C., Emini, E. A., & Scott, D. A. (2010). Immunogenicity and safety of 13-valent pneumococcal conjugate vaccine in infants and toddlers. Pediatrics, 126(3), e493-505. https://doi.org/10.1542/peds.2009-3027
Yeh SH, et al. Immunogenicity and Safety of 13-valent Pneumococcal Conjugate Vaccine in Infants and Toddlers. Pediatrics. 2010;126(3):e493-505. PubMed PMID: 20732948.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Immunogenicity and safety of 13-valent pneumococcal conjugate vaccine in infants and toddlers. AU - Yeh,Sylvia H, AU - Gurtman,Alejandra, AU - Hurley,David C, AU - Block,Stan L, AU - Schwartz,Richard H, AU - Patterson,Scott, AU - Jansen,Kathrin U, AU - Love,Jack, AU - Gruber,William C, AU - Emini,Emilio A, AU - Scott,Daniel A, AU - ,, Y1 - 2010/08/23/ PY - 2010/8/25/entrez PY - 2010/8/25/pubmed PY - 2010/10/5/medline SP - e493 EP - 505 JF - Pediatrics JO - Pediatrics VL - 126 IS - 3 N2 - BACKGROUND: 7-Valent pneumococcal conjugate vaccine (PCV7 [Prevnar, Wyeth Pharmaceuticals Inc, Philadelphia, PA], serotypes 4, 6B, 9V, 14, 18C, 19F, and 23F) is effective in preventing vaccine-serotype pneumococcal disease. 13-Valent pneumococcal conjugate vaccine (PCV13) (PCV7 serotypes plus 1, 3, 5, 6A, 7F, and 19A) was designed to provide broader pneumococcal disease coverage. We evaluated the immunogenicity and safety of PCV13 compared with PCV7. METHODS: Infants received PCV13 or PCV7 at ages 2, 4, 6, and 12 to 15 months with routine pediatric vaccinations. Pneumococcal anticapsular polysaccharide-binding immunoglobulin G responses and functional antipneumococcal opsonophagocytic activity were assessed 1 month after dose 3, before the toddler dose, and 1 month after the toddler dose. Safety and tolerability were also assessed. RESULTS: For the 7 common serotypes, PCV13-elicited immunoglobulin G titers were noninferior to those elicited by PCV7, although PCV13 responses were generally somewhat lower. PCV13 also elicited functional opsonophagocytic activity comparable with that elicited by PCV7. For the 6 additional serotypes in PCV13, PCV13 elicited binding and functional antibody levels notably greater than those in PCV7 recipients. After PCV13 immunization, concordance between antipolysaccharide and opsonophagocytic responses was noted for all 13 serotypes. The PCV13 toddler dose resulted in higher immune responses compared with infant-series doses. Safety and tolerability were comparable; reactogenicity was generally mild. CONCLUSIONS: PCV13 will be as effective as PCV7 in the prevention of pneumococcal disease caused by the 7 common serotypes and could provide expanded protection against the 6 additional serotypes. The PCV13 safety profile was comparable to that of PCV7. SN - 1098-4275 UR - https://www.unboundmedicine.com/medline/citation/20732948/Immunogenicity_and_safety_of_13_valent_pneumococcal_conjugate_vaccine_in_infants_and_toddlers_ L2 - https://publications.aap.org/pediatrics/article-lookup/doi/10.1542/peds.2009-3027 DB - PRIME DP - Unbound Medicine ER -