Journal article
Persistence of immunity following 2-dose priming with a 10-valent pneumococcal conjugate vaccine at 6 and 10 weeks or 6 and 14 weeks of age in Nepalese toddlers
- Abstract:
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Background:
The pneumococcal conjugate vaccine has had a substantial impact on invasive pneumococcal disease. Previously, we compared immunity following vaccination with the 10-valent pneumococcal conjugate vaccine (PCV10) administered at 2 slightly different schedules: at 6 and 10 weeks of age, and at 6 and 14 weeks of age, both followed by a 9-month booster. In this study, we followed up those participants to evaluate the medium-term persistence of serotype-specific pneumococcal immunity at 2-3 years of age.Method:
Children from the previous studies were contacted and after taking informed consent from their parents, blood samples and nasopharyngeal swabs were collected. Serotype-specific IgG antibody concentrations were determined by enzyme-linked immunosorbent assay, for the 10 vaccine serotypes, at a WHO pneumococcal serology reference laboratory.Findings:
Two hundred twenty of the 287 children who completed the primary study returned at 2–3 years of age to provide a blood sample and nasopharyngeal swab. The nasopharyngeal carriage rate of PCV10 serotypes in the 6 + 14 group was higher than the 6 + 10 group (13.4% vs. 1.9%). Nevertheless, the proportion of toddlers with serum pneumococcal serotype-specific IgG greater than or equal to 0.35 µg/mL was comparable for all PCV10 serotypes between the 6 + 10 week and 6 + 14 week groups. Similarly, the geometric mean concentrations of serum pneumococcal serotype-specific IgG levels were similar in the 2 groups for all serotypes, except for serotype 19F which was 32% lower in the 6 + 10 group than the 6 + 14 group.Conclusion:
Immunization with PCV10 at 6 + 10 weeks or 6 + 14 weeks, with a booster at 9 months in each case, results in similar persistence of serotype-specific antibody at 2-3 years of age. Thus, protection from pneumococcal disease is expected to be similar when either schedule is used.
- Publication status:
- Published
- Peer review status:
- Peer reviewed
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- Files:
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(Preview, Accepted manuscript, pdf, 402.7KB, Terms of use)
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- Publisher copy:
- 10.1097/inf.0000000000003223
Authors
- Publisher:
- Lippincott, Williams & Wilkins
- Journal:
- Pediatric Infectious Disease Journal More from this journal
- Volume:
- 40
- Issue:
- 10
- Pages:
- 937-943
- Publication date:
- 2021-07-20
- Acceptance date:
- 2021-04-30
- DOI:
- EISSN:
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1532-0987
- ISSN:
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0891-3668
- Pmid:
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34292271
- Language:
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English
- Keywords:
- Pubs id:
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1187637
- Local pid:
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pubs:1187637
- Deposit date:
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2021-09-21
- ARK identifier:
Terms of use
- Copyright holder:
- Wolters Kluwer Health, Inc.
- Copyright date:
- 2021
- Rights statement:
- Copyright © 2021 Wolters Kluwer Health, Inc. All rights reserved.
- Notes:
- This is the accepted manuscript version of the article. The final version is available online from Lippincott, Williams & Wilkins at: https://doi.org/10.1097/INF.0000000000003223
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