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STUDIES ON ANTIBODY PRODUCTION : XIII. THE EFFECT OF CHLORAMPHENICOL ON PRIMING IN MICE

Young adult mice were primed with 20 Lf (56 µg) of diphtheria toxoid and given a second injection of the same size 40 days later. This procedure produces a reproducible secondary response which can be used as a standard. Chloramphenicol in maximum dosage prevents the unknown process by which the ani...

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Autores principales: Cruchaud, Andre, Coons, Albert H.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1964
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2137794/
https://www.ncbi.nlm.nih.gov/pubmed/14238925
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author Cruchaud, Andre
Coons, Albert H.
author_facet Cruchaud, Andre
Coons, Albert H.
author_sort Cruchaud, Andre
collection PubMed
description Young adult mice were primed with 20 Lf (56 µg) of diphtheria toxoid and given a second injection of the same size 40 days later. This procedure produces a reproducible secondary response which can be used as a standard. Chloramphenicol in maximum dosage prevents the unknown process by which the animal is primed for the second response. To be fully inhibitory, the drug must be given from the hour of the first antigen injection in maximum dosage for 2 weeks. A delay of 48 hours in starting the drug allows completion of the priming process, and shorter delays produce partial inhibition. Hence the initiation of priming is a rapid process sensitive to chloramphenicol. Subsequent changes in the cell population necessary for the full development of priming are not sensitive to chloramphenicol. The secondary antibody response is not inhibited in mice by chloramphenicol at the doses employed.
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spelling pubmed-21377942008-04-17 STUDIES ON ANTIBODY PRODUCTION : XIII. THE EFFECT OF CHLORAMPHENICOL ON PRIMING IN MICE Cruchaud, Andre Coons, Albert H. J Exp Med Article Young adult mice were primed with 20 Lf (56 µg) of diphtheria toxoid and given a second injection of the same size 40 days later. This procedure produces a reproducible secondary response which can be used as a standard. Chloramphenicol in maximum dosage prevents the unknown process by which the animal is primed for the second response. To be fully inhibitory, the drug must be given from the hour of the first antigen injection in maximum dosage for 2 weeks. A delay of 48 hours in starting the drug allows completion of the priming process, and shorter delays produce partial inhibition. Hence the initiation of priming is a rapid process sensitive to chloramphenicol. Subsequent changes in the cell population necessary for the full development of priming are not sensitive to chloramphenicol. The secondary antibody response is not inhibited in mice by chloramphenicol at the doses employed. The Rockefeller University Press 1964-11-30 /pmc/articles/PMC2137794/ /pubmed/14238925 Text en Copyright © 1964 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
Cruchaud, Andre
Coons, Albert H.
STUDIES ON ANTIBODY PRODUCTION : XIII. THE EFFECT OF CHLORAMPHENICOL ON PRIMING IN MICE
title STUDIES ON ANTIBODY PRODUCTION : XIII. THE EFFECT OF CHLORAMPHENICOL ON PRIMING IN MICE
title_full STUDIES ON ANTIBODY PRODUCTION : XIII. THE EFFECT OF CHLORAMPHENICOL ON PRIMING IN MICE
title_fullStr STUDIES ON ANTIBODY PRODUCTION : XIII. THE EFFECT OF CHLORAMPHENICOL ON PRIMING IN MICE
title_full_unstemmed STUDIES ON ANTIBODY PRODUCTION : XIII. THE EFFECT OF CHLORAMPHENICOL ON PRIMING IN MICE
title_short STUDIES ON ANTIBODY PRODUCTION : XIII. THE EFFECT OF CHLORAMPHENICOL ON PRIMING IN MICE
title_sort studies on antibody production : xiii. the effect of chloramphenicol on priming in mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2137794/
https://www.ncbi.nlm.nih.gov/pubmed/14238925
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