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ENHANCEMENT OF ANTIBODY SYNTHESIS BY 6-MERCAPTOPURINE

The administration of 6-MP to rabbits led to either suppression or enhancement of antibody production, depending on when the drug was given in relation to the antigenic challenge. Maximum enhancement of antibody synthesis was found when a small dose of BGG was administered 5 days after the last dose...

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Detalles Bibliográficos
Autores principales: Chanmougan, Devendrathan, Schwartz, Robert S.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1966
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2138228/
https://www.ncbi.nlm.nih.gov/pubmed/4162484
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author Chanmougan, Devendrathan
Schwartz, Robert S.
author_facet Chanmougan, Devendrathan
Schwartz, Robert S.
author_sort Chanmougan, Devendrathan
collection PubMed
description The administration of 6-MP to rabbits led to either suppression or enhancement of antibody production, depending on when the drug was given in relation to the antigenic challenge. Maximum enhancement of antibody synthesis was found when a small dose of BGG was administered 5 days after the last dose of a 1 wk course of 6-MP. There were no indications that the macrophage system or immunological memory was affected in animals with augmented antibody synthesis. It was proposed that enhancement of antibody production by 6-MP was due to nucleic acids released from cells killed or injured by the drug. It was suggested that lymphocytes incorporating these nucleic acids were transformed into specialized cells capable of direct and immediate stimulation by antigen and lacking immunological memory (hemocytoblasts). A relatively small dose of antigen was apparently capable of stimulating all the hemocytoblasts representing a given clone) with the result that large amounts of antibody rapidly appeared in the serum.
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spelling pubmed-21382282008-04-17 ENHANCEMENT OF ANTIBODY SYNTHESIS BY 6-MERCAPTOPURINE Chanmougan, Devendrathan Schwartz, Robert S. J Exp Med Article The administration of 6-MP to rabbits led to either suppression or enhancement of antibody production, depending on when the drug was given in relation to the antigenic challenge. Maximum enhancement of antibody synthesis was found when a small dose of BGG was administered 5 days after the last dose of a 1 wk course of 6-MP. There were no indications that the macrophage system or immunological memory was affected in animals with augmented antibody synthesis. It was proposed that enhancement of antibody production by 6-MP was due to nucleic acids released from cells killed or injured by the drug. It was suggested that lymphocytes incorporating these nucleic acids were transformed into specialized cells capable of direct and immediate stimulation by antigen and lacking immunological memory (hemocytoblasts). A relatively small dose of antigen was apparently capable of stimulating all the hemocytoblasts representing a given clone) with the result that large amounts of antibody rapidly appeared in the serum. The Rockefeller University Press 1966-09-01 /pmc/articles/PMC2138228/ /pubmed/4162484 Text en Copyright © 1966 by The Rockefeller University Press 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
Chanmougan, Devendrathan
Schwartz, Robert S.
ENHANCEMENT OF ANTIBODY SYNTHESIS BY 6-MERCAPTOPURINE
title ENHANCEMENT OF ANTIBODY SYNTHESIS BY 6-MERCAPTOPURINE
title_full ENHANCEMENT OF ANTIBODY SYNTHESIS BY 6-MERCAPTOPURINE
title_fullStr ENHANCEMENT OF ANTIBODY SYNTHESIS BY 6-MERCAPTOPURINE
title_full_unstemmed ENHANCEMENT OF ANTIBODY SYNTHESIS BY 6-MERCAPTOPURINE
title_short ENHANCEMENT OF ANTIBODY SYNTHESIS BY 6-MERCAPTOPURINE
title_sort enhancement of antibody synthesis by 6-mercaptopurine
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2138228/
https://www.ncbi.nlm.nih.gov/pubmed/4162484
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