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Evaluation of antibody responses to pneumococcal vaccines with ELISA and opsonophagocytic assay.

Antibodies to a capsular polysaccharide (PS) provide protection against Streptococcus pneumoniae which express the homologous capsular serotype, and pneumococcal vaccines are designed to induce antibodies in the capsular PS. Levels and opsonophagocytic capacity of antibodies to the capsular PS of S....

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Detalles Bibliográficos
Autores principales: Kim, K. H., Seoh, J. Y.
Formato: Texto
Lenguaje:English
Publicado: Korean Academy of Medical Sciences 1999
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3054463/
https://www.ncbi.nlm.nih.gov/pubmed/10576141
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author Kim, K. H.
Seoh, J. Y.
author_facet Kim, K. H.
Seoh, J. Y.
author_sort Kim, K. H.
collection PubMed
description Antibodies to a capsular polysaccharide (PS) provide protection against Streptococcus pneumoniae which express the homologous capsular serotype, and pneumococcal vaccines are designed to induce antibodies in the capsular PS. Levels and opsonophagocytic capacity of antibodies to the capsular PS of S. pneumoniae serotype 19F were determined by sera from adults immunized with 23-valent S. pneumoniae capsular PS vaccines. Geometric means of IgG anti-19F antibody level and specific opsonic titer rise significantly after immunization. The level of anticapsular PS antibodies for S. pneumoniae 19F serotype is fairly well correlated (r2=O.63) with the opsonophagocytic activities of sera. However, 3.7% (1/27) of serum samples display strikingly less opsonophagocytic activity than expected on the basis of their antibody level. Thus, antibody level may be of general use in predicting vaccine-induced protection among adults for 19F serotype. However, the opsonic activity data suggest that antibody levels are not always indicative of functional antibody.
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spelling pubmed-30544632011-03-15 Evaluation of antibody responses to pneumococcal vaccines with ELISA and opsonophagocytic assay. Kim, K. H. Seoh, J. Y. J Korean Med Sci Research Article Antibodies to a capsular polysaccharide (PS) provide protection against Streptococcus pneumoniae which express the homologous capsular serotype, and pneumococcal vaccines are designed to induce antibodies in the capsular PS. Levels and opsonophagocytic capacity of antibodies to the capsular PS of S. pneumoniae serotype 19F were determined by sera from adults immunized with 23-valent S. pneumoniae capsular PS vaccines. Geometric means of IgG anti-19F antibody level and specific opsonic titer rise significantly after immunization. The level of anticapsular PS antibodies for S. pneumoniae 19F serotype is fairly well correlated (r2=O.63) with the opsonophagocytic activities of sera. However, 3.7% (1/27) of serum samples display strikingly less opsonophagocytic activity than expected on the basis of their antibody level. Thus, antibody level may be of general use in predicting vaccine-induced protection among adults for 19F serotype. However, the opsonic activity data suggest that antibody levels are not always indicative of functional antibody. Korean Academy of Medical Sciences 1999-10 /pmc/articles/PMC3054463/ /pubmed/10576141 Text en
spellingShingle Research Article
Kim, K. H.
Seoh, J. Y.
Evaluation of antibody responses to pneumococcal vaccines with ELISA and opsonophagocytic assay.
title Evaluation of antibody responses to pneumococcal vaccines with ELISA and opsonophagocytic assay.
title_full Evaluation of antibody responses to pneumococcal vaccines with ELISA and opsonophagocytic assay.
title_fullStr Evaluation of antibody responses to pneumococcal vaccines with ELISA and opsonophagocytic assay.
title_full_unstemmed Evaluation of antibody responses to pneumococcal vaccines with ELISA and opsonophagocytic assay.
title_short Evaluation of antibody responses to pneumococcal vaccines with ELISA and opsonophagocytic assay.
title_sort evaluation of antibody responses to pneumococcal vaccines with elisa and opsonophagocytic assay.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3054463/
https://www.ncbi.nlm.nih.gov/pubmed/10576141
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