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A STUDY OF PASSIVE IMMUNITY TO MENINGOCOCCUS INFECTION IN THE CHICK EMBRYO

1. 14 day old chick embryos are protected against subsequent meningococcus infection through the amniotic route by the intravenous administration of an homologous antiserum produced in hens, by a commercial concentrated polyvalent meningococcus antiserum and by a commercial meningococcus antitoxin....

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Detalles Bibliográficos
Autores principales: Buddingh, G. John, Polk, Alice D.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1939
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2133805/
https://www.ncbi.nlm.nih.gov/pubmed/19870927
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author Buddingh, G. John
Polk, Alice D.
author_facet Buddingh, G. John
Polk, Alice D.
author_sort Buddingh, G. John
collection PubMed
description 1. 14 day old chick embryos are protected against subsequent meningococcus infection through the amniotic route by the intravenous administration of an homologous antiserum produced in hens, by a commercial concentrated polyvalent meningococcus antiserum and by a commercial meningococcus antitoxin. 2. Titrations of the different antisera indicate that the homologous and commercial polyvalent sera have approximately the same protective value and are much more effective than the commercial antitoxin. The titrations also show that the chick embryo is a sensitive indicator of the amount of antibodies present in a given amount of serum. 3. The mechanism of the protective action of the antisera is not apparent from these experiments except that in the treated embryos there is a relative inhibition of the growth and presumably a neutralization of the injurious products of the meningococci.
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spelling pubmed-21338052008-04-18 A STUDY OF PASSIVE IMMUNITY TO MENINGOCOCCUS INFECTION IN THE CHICK EMBRYO Buddingh, G. John Polk, Alice D. J Exp Med Article 1. 14 day old chick embryos are protected against subsequent meningococcus infection through the amniotic route by the intravenous administration of an homologous antiserum produced in hens, by a commercial concentrated polyvalent meningococcus antiserum and by a commercial meningococcus antitoxin. 2. Titrations of the different antisera indicate that the homologous and commercial polyvalent sera have approximately the same protective value and are much more effective than the commercial antitoxin. The titrations also show that the chick embryo is a sensitive indicator of the amount of antibodies present in a given amount of serum. 3. The mechanism of the protective action of the antisera is not apparent from these experiments except that in the treated embryos there is a relative inhibition of the growth and presumably a neutralization of the injurious products of the meningococci. The Rockefeller University Press 1939-10-31 /pmc/articles/PMC2133805/ /pubmed/19870927 Text en Copyright © Copyright, 1939, by The Rockefeller Institute for Medical Research New York 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 Article
Buddingh, G. John
Polk, Alice D.
A STUDY OF PASSIVE IMMUNITY TO MENINGOCOCCUS INFECTION IN THE CHICK EMBRYO
title A STUDY OF PASSIVE IMMUNITY TO MENINGOCOCCUS INFECTION IN THE CHICK EMBRYO
title_full A STUDY OF PASSIVE IMMUNITY TO MENINGOCOCCUS INFECTION IN THE CHICK EMBRYO
title_fullStr A STUDY OF PASSIVE IMMUNITY TO MENINGOCOCCUS INFECTION IN THE CHICK EMBRYO
title_full_unstemmed A STUDY OF PASSIVE IMMUNITY TO MENINGOCOCCUS INFECTION IN THE CHICK EMBRYO
title_short A STUDY OF PASSIVE IMMUNITY TO MENINGOCOCCUS INFECTION IN THE CHICK EMBRYO
title_sort study of passive immunity to meningococcus infection in the chick embryo
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2133805/
https://www.ncbi.nlm.nih.gov/pubmed/19870927
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