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GENETICS OF RESTRICTED ANTIBODIES TO STREPTOCOCCAL GROUP POLYSACCHARIDES IN MICE : I. STRAIN DIFFERENCES OF ISOELECTRIC FOCUSING SPECTRA OF GROUP A HYPERIMMUNE ANTISERA

The immune response of nine inbred and one outbred strain of mice to the streptococcal group A polysaccharide was investigated with respect to magnitude and restriction. Analytical isoelectric focusing served as a tool to estimate the degree of restriction of Group A polysaccharide-specific antibodi...

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Autores principales: Cramer, Matthias, Braun, Dietmar G.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1974
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2139689/
https://www.ncbi.nlm.nih.gov/pubmed/4133618
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author Cramer, Matthias
Braun, Dietmar G.
author_facet Cramer, Matthias
Braun, Dietmar G.
author_sort Cramer, Matthias
collection PubMed
description The immune response of nine inbred and one outbred strain of mice to the streptococcal group A polysaccharide was investigated with respect to magnitude and restriction. Analytical isoelectric focusing served as a tool to estimate the degree of restriction of Group A polysaccharide-specific antibodies. It proved feasible to distinguish low and intermediate from high responder strains, and to delineate strain-specificity of isoelectric focusing spectra of the immune sera. For example, immune sera of BALB/c mice, restricted high responders, and of C57BL/6 mice, heterogeneous low responders, had distinct focusing properties. Responsiveness was a dominant autosomal genetic trait in C57BL/6 x BALB/c F(1) hybrid mice, irrespective of the maternal and the paternal genotype; the immune sera of these mice had their own, rather uniform isoelectric focusing spectra whereby structural genes of the low responder strain were expressed to predominant levels in 81% of the hybrids. Responsiveness in C57BL/6 x BALB/c F(2) progeny segregated into 79% high and 21% low responders, and showed no genetic linkage to the following characteristics: hair color, sex, H-2 type, and Ig allotype of the heavy chain. The isoelectric focusing properties of these immune sera indicated segregation into patterns like BALB/c mice (40%), F(1) hybrids (48%), and C57BL/6 mice (12%). Since this segregation is independent of any of the above criteria in these F(2) mice a regulatory gene(s) is postulated that controls the clonal pattern of the immune response.
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spelling pubmed-21396892008-04-17 GENETICS OF RESTRICTED ANTIBODIES TO STREPTOCOCCAL GROUP POLYSACCHARIDES IN MICE : I. STRAIN DIFFERENCES OF ISOELECTRIC FOCUSING SPECTRA OF GROUP A HYPERIMMUNE ANTISERA Cramer, Matthias Braun, Dietmar G. J Exp Med Article The immune response of nine inbred and one outbred strain of mice to the streptococcal group A polysaccharide was investigated with respect to magnitude and restriction. Analytical isoelectric focusing served as a tool to estimate the degree of restriction of Group A polysaccharide-specific antibodies. It proved feasible to distinguish low and intermediate from high responder strains, and to delineate strain-specificity of isoelectric focusing spectra of the immune sera. For example, immune sera of BALB/c mice, restricted high responders, and of C57BL/6 mice, heterogeneous low responders, had distinct focusing properties. Responsiveness was a dominant autosomal genetic trait in C57BL/6 x BALB/c F(1) hybrid mice, irrespective of the maternal and the paternal genotype; the immune sera of these mice had their own, rather uniform isoelectric focusing spectra whereby structural genes of the low responder strain were expressed to predominant levels in 81% of the hybrids. Responsiveness in C57BL/6 x BALB/c F(2) progeny segregated into 79% high and 21% low responders, and showed no genetic linkage to the following characteristics: hair color, sex, H-2 type, and Ig allotype of the heavy chain. The isoelectric focusing properties of these immune sera indicated segregation into patterns like BALB/c mice (40%), F(1) hybrids (48%), and C57BL/6 mice (12%). Since this segregation is independent of any of the above criteria in these F(2) mice a regulatory gene(s) is postulated that controls the clonal pattern of the immune response. The Rockefeller University Press 1974-06-01 /pmc/articles/PMC2139689/ /pubmed/4133618 Text en Copyright © 1974 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
Cramer, Matthias
Braun, Dietmar G.
GENETICS OF RESTRICTED ANTIBODIES TO STREPTOCOCCAL GROUP POLYSACCHARIDES IN MICE : I. STRAIN DIFFERENCES OF ISOELECTRIC FOCUSING SPECTRA OF GROUP A HYPERIMMUNE ANTISERA
title GENETICS OF RESTRICTED ANTIBODIES TO STREPTOCOCCAL GROUP POLYSACCHARIDES IN MICE : I. STRAIN DIFFERENCES OF ISOELECTRIC FOCUSING SPECTRA OF GROUP A HYPERIMMUNE ANTISERA
title_full GENETICS OF RESTRICTED ANTIBODIES TO STREPTOCOCCAL GROUP POLYSACCHARIDES IN MICE : I. STRAIN DIFFERENCES OF ISOELECTRIC FOCUSING SPECTRA OF GROUP A HYPERIMMUNE ANTISERA
title_fullStr GENETICS OF RESTRICTED ANTIBODIES TO STREPTOCOCCAL GROUP POLYSACCHARIDES IN MICE : I. STRAIN DIFFERENCES OF ISOELECTRIC FOCUSING SPECTRA OF GROUP A HYPERIMMUNE ANTISERA
title_full_unstemmed GENETICS OF RESTRICTED ANTIBODIES TO STREPTOCOCCAL GROUP POLYSACCHARIDES IN MICE : I. STRAIN DIFFERENCES OF ISOELECTRIC FOCUSING SPECTRA OF GROUP A HYPERIMMUNE ANTISERA
title_short GENETICS OF RESTRICTED ANTIBODIES TO STREPTOCOCCAL GROUP POLYSACCHARIDES IN MICE : I. STRAIN DIFFERENCES OF ISOELECTRIC FOCUSING SPECTRA OF GROUP A HYPERIMMUNE ANTISERA
title_sort genetics of restricted antibodies to streptococcal group polysaccharides in mice : i. strain differences of isoelectric focusing spectra of group a hyperimmune antisera
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2139689/
https://www.ncbi.nlm.nih.gov/pubmed/4133618
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