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TOLERANCE AND IMMUNITY TO MATERNALLY DERIVED INCOMPATIBLE IgG(2a)-GLOBULIN IN MICE

Progeny mice were confronted with maternal γ-globulin of a different allotype by either back-cross mating, intercross mating, or by foster nursing. In all cases, many mice subsequently produced alloantibodies directed against the incompatible maternal type of IgG(2a)-globulin. In one series of exper...

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Detalles Bibliográficos
Autores principales: Warner, Noel L., Herzenberg, Leonore A.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1970
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2138803/
https://www.ncbi.nlm.nih.gov/pubmed/5316260
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author Warner, Noel L.
Herzenberg, Leonore A.
author_facet Warner, Noel L.
Herzenberg, Leonore A.
author_sort Warner, Noel L.
collection PubMed
description Progeny mice were confronted with maternal γ-globulin of a different allotype by either back-cross mating, intercross mating, or by foster nursing. In all cases, many mice subsequently produced alloantibodies directed against the incompatible maternal type of IgG(2a)-globulin. In one series of experiments, immunologic tolerance to the maternally derived γ-globulin was demonstrated to exist in the period before formation of spontaneous antibody. The state of tolerance was then lost, unless maintenance injections of foreign γ-globulin were given. These studies demonstrate in a natural situation that maternally derived foreign proteins can first induce a state of immunological tolerance which is followed, after disappearance of the antigen, by a state of immunity. As such, this parallels the experimental induction of tolerance to foreign proteins by neonatal injections.
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spelling pubmed-21388032008-04-17 TOLERANCE AND IMMUNITY TO MATERNALLY DERIVED INCOMPATIBLE IgG(2a)-GLOBULIN IN MICE Warner, Noel L. Herzenberg, Leonore A. J Exp Med Article Progeny mice were confronted with maternal γ-globulin of a different allotype by either back-cross mating, intercross mating, or by foster nursing. In all cases, many mice subsequently produced alloantibodies directed against the incompatible maternal type of IgG(2a)-globulin. In one series of experiments, immunologic tolerance to the maternally derived γ-globulin was demonstrated to exist in the period before formation of spontaneous antibody. The state of tolerance was then lost, unless maintenance injections of foreign γ-globulin were given. These studies demonstrate in a natural situation that maternally derived foreign proteins can first induce a state of immunological tolerance which is followed, after disappearance of the antigen, by a state of immunity. As such, this parallels the experimental induction of tolerance to foreign proteins by neonatal injections. The Rockefeller University Press 1970-09-01 /pmc/articles/PMC2138803/ /pubmed/5316260 Text en Copyright © 1970 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
Warner, Noel L.
Herzenberg, Leonore A.
TOLERANCE AND IMMUNITY TO MATERNALLY DERIVED INCOMPATIBLE IgG(2a)-GLOBULIN IN MICE
title TOLERANCE AND IMMUNITY TO MATERNALLY DERIVED INCOMPATIBLE IgG(2a)-GLOBULIN IN MICE
title_full TOLERANCE AND IMMUNITY TO MATERNALLY DERIVED INCOMPATIBLE IgG(2a)-GLOBULIN IN MICE
title_fullStr TOLERANCE AND IMMUNITY TO MATERNALLY DERIVED INCOMPATIBLE IgG(2a)-GLOBULIN IN MICE
title_full_unstemmed TOLERANCE AND IMMUNITY TO MATERNALLY DERIVED INCOMPATIBLE IgG(2a)-GLOBULIN IN MICE
title_short TOLERANCE AND IMMUNITY TO MATERNALLY DERIVED INCOMPATIBLE IgG(2a)-GLOBULIN IN MICE
title_sort tolerance and immunity to maternally derived incompatible igg(2a)-globulin in mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2138803/
https://www.ncbi.nlm.nih.gov/pubmed/5316260
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