Cited by 76Bacterial Infections and VaccinesImmune responses and vaccinationsCarbohydrate Chemistry and Synthesis

Carrier priming or suppression: Understanding carrier priming enhancement of anti-polysaccharide antibody response to conjugate vaccines

Pobre, Karl, Tashani, Mohamed, Ridda, Iman, Rashid, Harunor, Wong, Melanie, Booy, Robert·2014·Vaccine

Abstract

Introduction With the availability of newer conjugate vaccines, immunization schedules have become increasingly complex due to the potential for unpredictable immunologic interference such as 'carrier priming' and 'carrier induced epitopic suppression'. Carrier priming refers to an augmented antibody response to a carbohydrate portion of a glycoconjugate vaccine in an individual previously primed with the carrier protein. This review aims to provide a critical evaluation of the available data on carrier priming (and suppression) and conceptualize ways by which this phenomenon can be utilized to strengthen vaccination schedules. Methods We conducted this literature review by searching well-known databases to date to identify relevant studies, then extracted and synthesized the data on carrier priming of widely used conjugate polysaccharide vaccines, such as, pneumococcal conjugate vaccine (PCV), meningococcal conjugate vaccine (MenCV) and Haemophilus influenzae type b conjugate vaccines (HibV). Results We found evidence of carrier priming with some conjugate vaccines, particularly HibV and PCV, in both animal and human models but controversy surrounds MenCV. This has implications for the immunogenicity of conjugate polysaccharide vaccines following the administration of tetanus-toxoid or diphtheria-toxoid containing vaccine (such as DTP). Conclusion Available evidence supports a promising role for carrier priming in terms of maximizing the immunogenicity of conjugate vaccines and enhancing immunization schedule by making it more efficient and cost effective.

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Crossref · 10.1016/j.vaccine.2014.01.047

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Authors
Pobre, K., Tashani, M., Ridda, I., Rashid, H., Wong, M., & Booy, R.
Affiliations
  • Children's Hospital at Westmead (AU)
  • The University of Sydney (AU)
Corresponding author
Tashani, Mohamed
Venue
Vaccine
Publisher
Elsevier BV
Published
2014-03
Volume
32
Issue
13
Pages
1423-1430
ISSN
0264-410X (ISSN-L)
OpenAlex
W2076935057
Cited by
76
References
3
Citations by year
2026: 8 · 2025: 3 · 2024: 3 · 2023: 4 · 2022: 5 · 2021: 6 · 2020: 8 · 2019: 7 · 2018: 4 · 2017: 4 · 2016: 13 · 2015: 7 · 2014: 4
FWCI
1.28
Type
journal article
Language
en
Open access
closed
Locations
  • Vaccine (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • Merck
  • National Health and Medical Research Council (630739)
  • GlaxoSmithKline
Topics
  • Life Sciences › Immunology and Microbiology › Microbiology › Bacterial Infections and Vaccines
  • Life Sciences › Immunology and Microbiology › Immunology › Immune responses and vaccinations
  • Physical Sciences › Chemistry › Organic Chemistry › Carbohydrate Chemistry and Synthesis
Keywords
carrier suppression, conjugate vaccines, polysaccharide vaccine, pneumococcal conjugate vaccine, meningococcal conjugate vaccine, Haemophilus influenzae type b conjugate vaccine, tetanus toxoid, diphtheria toxoid, immunogenicity, vaccination schedule, antibody response
MeSH terms
Animals, Antibody Formation, Drug Carriers, Humans, Immunization Schedule, Polysaccharides, Bacterial Capsules, Haemophilus Vaccines, Vaccines, Conjugate, Pneumococcal Vaccines, Meningococcal Vaccines

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