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STUDIES ON ANTIBODY PRODUCTION : XII. INHIBITION OF PRIMING BY DRUGS

The effect of drugs upon the primary and the secondary antibody response to diphtheria toxoid in mice was studied using an experimental system previously described. Triethylenethiophosphoramide (thio-TEPA), chloramphenicol, 6-mercaptopurine, 8-azaguanine, and versenate were found to inhibit, partial...

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Detalles Bibliográficos
Autores principales: Butler, William T., 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/PMC2137792/
https://www.ncbi.nlm.nih.gov/pubmed/14238924
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author Butler, William T.
Coons, Albert H.
author_facet Butler, William T.
Coons, Albert H.
author_sort Butler, William T.
collection PubMed
description The effect of drugs upon the primary and the secondary antibody response to diphtheria toxoid in mice was studied using an experimental system previously described. Triethylenethiophosphoramide (thio-TEPA), chloramphenicol, 6-mercaptopurine, 8-azaguanine, and versenate were found to inhibit, partially or completely,"priming" for the secondary response. Thio-TEPA, chloramphenicol, and 6-mercaptopurine, in doses exceeding those effective in inhibiting priming, did not cause alteration of the secondary response when given only during the secondary response. However, when chloramphenicol and amethopterin were given for 5 days prior to and at least 5 days after the second antigen injection, slight suppression of peak secondary titers occurred. Therefore, drug dosages effective in suppressing priming had less effect on the secondary response. It thus appears that there is a real difference between "priming" and the induction of antibody synthesis.
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spelling pubmed-21377922008-04-17 STUDIES ON ANTIBODY PRODUCTION : XII. INHIBITION OF PRIMING BY DRUGS Butler, William T. Coons, Albert H. J Exp Med Article The effect of drugs upon the primary and the secondary antibody response to diphtheria toxoid in mice was studied using an experimental system previously described. Triethylenethiophosphoramide (thio-TEPA), chloramphenicol, 6-mercaptopurine, 8-azaguanine, and versenate were found to inhibit, partially or completely,"priming" for the secondary response. Thio-TEPA, chloramphenicol, and 6-mercaptopurine, in doses exceeding those effective in inhibiting priming, did not cause alteration of the secondary response when given only during the secondary response. However, when chloramphenicol and amethopterin were given for 5 days prior to and at least 5 days after the second antigen injection, slight suppression of peak secondary titers occurred. Therefore, drug dosages effective in suppressing priming had less effect on the secondary response. It thus appears that there is a real difference between "priming" and the induction of antibody synthesis. The Rockefeller University Press 1964-11-30 /pmc/articles/PMC2137792/ /pubmed/14238924 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
Butler, William T.
Coons, Albert H.
STUDIES ON ANTIBODY PRODUCTION : XII. INHIBITION OF PRIMING BY DRUGS
title STUDIES ON ANTIBODY PRODUCTION : XII. INHIBITION OF PRIMING BY DRUGS
title_full STUDIES ON ANTIBODY PRODUCTION : XII. INHIBITION OF PRIMING BY DRUGS
title_fullStr STUDIES ON ANTIBODY PRODUCTION : XII. INHIBITION OF PRIMING BY DRUGS
title_full_unstemmed STUDIES ON ANTIBODY PRODUCTION : XII. INHIBITION OF PRIMING BY DRUGS
title_short STUDIES ON ANTIBODY PRODUCTION : XII. INHIBITION OF PRIMING BY DRUGS
title_sort studies on antibody production : xii. inhibition of priming by drugs
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2137792/
https://www.ncbi.nlm.nih.gov/pubmed/14238924
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