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Pneumococcal Conjugate Vaccine for Adults: A New Paradigm

A 13-valent pneumococcal conjugate vaccine has been studied in adults aged ≥50 years to compare the immune response to that induced by the 23-valent pneumococcal polysaccharide vaccine, which has been the standard of care over the past 30 years. The results demonstrate that adults, regardless of whe...

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Detalles Bibliográficos
Autor principal: Paradiso, Peter R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3381637/
https://www.ncbi.nlm.nih.gov/pubmed/22495545
http://dx.doi.org/10.1093/cid/cis359
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author Paradiso, Peter R.
author_facet Paradiso, Peter R.
author_sort Paradiso, Peter R.
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description A 13-valent pneumococcal conjugate vaccine has been studied in adults aged ≥50 years to compare the immune response to that induced by the 23-valent pneumococcal polysaccharide vaccine, which has been the standard of care over the past 30 years. The results demonstrate that adults, regardless of whether they are naive or previously vaccinated with the polysaccharide vaccine, have an overall superior antibody response when vaccinated with the conjugate vaccine compared with the pneumococcal polysaccharide vaccine. More importantly, the nature of the response is indicative of a T-cell–dependent response that elicits immunological memory and, therefore, primes the immune system for either natural exposure or subsequent booster vaccination with either conjugate or polysaccharide vaccine. The conjugate vaccine, which has been successful in reducing pneumococcal disease in children, now provides a new approach to preventing pneumococcal disease, including community-acquired pneumonia, in adults.
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spelling pubmed-33816372012-06-25 Pneumococcal Conjugate Vaccine for Adults: A New Paradigm Paradiso, Peter R. Clin Infect Dis Invited Article A 13-valent pneumococcal conjugate vaccine has been studied in adults aged ≥50 years to compare the immune response to that induced by the 23-valent pneumococcal polysaccharide vaccine, which has been the standard of care over the past 30 years. The results demonstrate that adults, regardless of whether they are naive or previously vaccinated with the polysaccharide vaccine, have an overall superior antibody response when vaccinated with the conjugate vaccine compared with the pneumococcal polysaccharide vaccine. More importantly, the nature of the response is indicative of a T-cell–dependent response that elicits immunological memory and, therefore, primes the immune system for either natural exposure or subsequent booster vaccination with either conjugate or polysaccharide vaccine. The conjugate vaccine, which has been successful in reducing pneumococcal disease in children, now provides a new approach to preventing pneumococcal disease, including community-acquired pneumonia, in adults. Oxford University Press 2012-07-15 2012-04-11 /pmc/articles/PMC3381637/ /pubmed/22495545 http://dx.doi.org/10.1093/cid/cis359 Text en © The Author 2012. Published by Oxford University Press on behalf of the Infectious Diseases Society of America. All rights reserved. For Permissions, please e-mail: journals.permissions@oup.com. This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0), which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Invited Article
Paradiso, Peter R.
Pneumococcal Conjugate Vaccine for Adults: A New Paradigm
title Pneumococcal Conjugate Vaccine for Adults: A New Paradigm
title_full Pneumococcal Conjugate Vaccine for Adults: A New Paradigm
title_fullStr Pneumococcal Conjugate Vaccine for Adults: A New Paradigm
title_full_unstemmed Pneumococcal Conjugate Vaccine for Adults: A New Paradigm
title_short Pneumococcal Conjugate Vaccine for Adults: A New Paradigm
title_sort pneumococcal conjugate vaccine for adults: a new paradigm
topic Invited Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3381637/
https://www.ncbi.nlm.nih.gov/pubmed/22495545
http://dx.doi.org/10.1093/cid/cis359
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