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Protection against group B meningococcal disease. II. Infection and resulting immunity in a guinea pig model
A guinea pig subcutaneous chamber model was used to evaluate the specificity of the immune response resulting from Neisseria meningitidis infection. Small numbers of meningococci easily infected the chambers. The infections persisted for 6-8 days with relatively high levels of organisms (10(5)-10(6)...
Formato: | Texto |
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Lenguaje: | English |
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The Rockefeller University Press
1978
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2184191/ https://www.ncbi.nlm.nih.gov/pubmed/416163 |
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collection | PubMed |
description | A guinea pig subcutaneous chamber model was used to evaluate the specificity of the immune response resulting from Neisseria meningitidis infection. Small numbers of meningococci easily infected the chambers. The infections persisted for 6-8 days with relatively high levels of organisms (10(5)-10(6)/milliliter) in the chambers, and were then rapidly eliminated and no organisms could be cultured beyond day 14. Clearance of infection correlated with appearance of circulating antibody. Antibody against both the protein serotype antigen and the capsular polysaccharide were induced as a result of meningococcal infection. The group-specific polysaccharide response peaked 2-3 wk after the animals were inoculated, while the type- specific protein response peaked at 5-6 wk. The animals were quite resistant to reinfection with either the homologous serogroup or serotype. |
format | Text |
id | pubmed-2184191 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1978 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21841912008-04-17 Protection against group B meningococcal disease. II. Infection and resulting immunity in a guinea pig model J Exp Med Articles A guinea pig subcutaneous chamber model was used to evaluate the specificity of the immune response resulting from Neisseria meningitidis infection. Small numbers of meningococci easily infected the chambers. The infections persisted for 6-8 days with relatively high levels of organisms (10(5)-10(6)/milliliter) in the chambers, and were then rapidly eliminated and no organisms could be cultured beyond day 14. Clearance of infection correlated with appearance of circulating antibody. Antibody against both the protein serotype antigen and the capsular polysaccharide were induced as a result of meningococcal infection. The group-specific polysaccharide response peaked 2-3 wk after the animals were inoculated, while the type- specific protein response peaked at 5-6 wk. The animals were quite resistant to reinfection with either the homologous serogroup or serotype. The Rockefeller University Press 1978-03-01 /pmc/articles/PMC2184191/ /pubmed/416163 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Articles Protection against group B meningococcal disease. II. Infection and resulting immunity in a guinea pig model |
title | Protection against group B meningococcal disease. II. Infection and resulting immunity in a guinea pig model |
title_full | Protection against group B meningococcal disease. II. Infection and resulting immunity in a guinea pig model |
title_fullStr | Protection against group B meningococcal disease. II. Infection and resulting immunity in a guinea pig model |
title_full_unstemmed | Protection against group B meningococcal disease. II. Infection and resulting immunity in a guinea pig model |
title_short | Protection against group B meningococcal disease. II. Infection and resulting immunity in a guinea pig model |
title_sort | protection against group b meningococcal disease. ii. infection and resulting immunity in a guinea pig model |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2184191/ https://www.ncbi.nlm.nih.gov/pubmed/416163 |