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ANTIBODY FORMATION : II. THE SPECIFIC ANAMNESTIC ANTIBODY RESPONSE

Diphtheria toxoid-antitoxin precipitates formed in antitoxin excess can prepare guinea pigs, rats, and rabbits for a secondary type of antitoxin response. Priming may occur without the development of detectable serum antibody. In rats, toxoid-antitoxin precipitates are more efficient than "free...

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Detalles Bibliográficos
Autores principales: Uhr, Jonathan W., Baumann, Joyce B.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1961
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2137413/
https://www.ncbi.nlm.nih.gov/pubmed/13779028
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author Uhr, Jonathan W.
Baumann, Joyce B.
author_facet Uhr, Jonathan W.
Baumann, Joyce B.
author_sort Uhr, Jonathan W.
collection PubMed
description Diphtheria toxoid-antitoxin precipitates formed in antitoxin excess can prepare guinea pigs, rats, and rabbits for a secondary type of antitoxin response. Priming may occur without the development of detectable serum antibody. In rats, toxoid-antitoxin precipitates are more efficient than "free" toxoid in priming, whereas in guinea pigs, the magnitude of the anamnestic response varies with the precipitate employed. The possibility that priming is due to "free" antigen released from the specific precipitate rather than the precipitate itself is discussed. The anamnestic antitoxin response can be inhibited by passive antitoxin, but less efficiently than primary antitoxin formation. Partial suppression of the secondary antitoxin response was accomplished by injection of excess horse antitoxin as long as 4 days after reimmunization with toxoid. The importance of these findings for the understanding of passive-active immunization in the human is discussed.
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spelling pubmed-21374132008-04-17 ANTIBODY FORMATION : II. THE SPECIFIC ANAMNESTIC ANTIBODY RESPONSE Uhr, Jonathan W. Baumann, Joyce B. J Exp Med Article Diphtheria toxoid-antitoxin precipitates formed in antitoxin excess can prepare guinea pigs, rats, and rabbits for a secondary type of antitoxin response. Priming may occur without the development of detectable serum antibody. In rats, toxoid-antitoxin precipitates are more efficient than "free" toxoid in priming, whereas in guinea pigs, the magnitude of the anamnestic response varies with the precipitate employed. The possibility that priming is due to "free" antigen released from the specific precipitate rather than the precipitate itself is discussed. The anamnestic antitoxin response can be inhibited by passive antitoxin, but less efficiently than primary antitoxin formation. Partial suppression of the secondary antitoxin response was accomplished by injection of excess horse antitoxin as long as 4 days after reimmunization with toxoid. The importance of these findings for the understanding of passive-active immunization in the human is discussed. The Rockefeller University Press 1961-05-01 /pmc/articles/PMC2137413/ /pubmed/13779028 Text en Copyright © Copyright, 1961, by The Rockefeller Institute 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
Uhr, Jonathan W.
Baumann, Joyce B.
ANTIBODY FORMATION : II. THE SPECIFIC ANAMNESTIC ANTIBODY RESPONSE
title ANTIBODY FORMATION : II. THE SPECIFIC ANAMNESTIC ANTIBODY RESPONSE
title_full ANTIBODY FORMATION : II. THE SPECIFIC ANAMNESTIC ANTIBODY RESPONSE
title_fullStr ANTIBODY FORMATION : II. THE SPECIFIC ANAMNESTIC ANTIBODY RESPONSE
title_full_unstemmed ANTIBODY FORMATION : II. THE SPECIFIC ANAMNESTIC ANTIBODY RESPONSE
title_short ANTIBODY FORMATION : II. THE SPECIFIC ANAMNESTIC ANTIBODY RESPONSE
title_sort antibody formation : ii. the specific anamnestic antibody response
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2137413/
https://www.ncbi.nlm.nih.gov/pubmed/13779028
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