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Coupled complementation of immune response genes controlling responsiveness to the H-2.2 alloantigen

The ability of various B10 congenic resistant strains to respond to the alloantigen H-2.2 was tested. High and low antibody-producing strains were distinguished by their anti-H-2.2 hemagglutinating respones. However, these strains do not differ in their ability to respond to these antigenic differen...

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Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1977
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2180781/
https://www.ncbi.nlm.nih.gov/pubmed/141489
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collection PubMed
description The ability of various B10 congenic resistant strains to respond to the alloantigen H-2.2 was tested. High and low antibody-producing strains were distinguished by their anti-H-2.2 hemagglutinating respones. However, these strains do not differ in their ability to respond to these antigenic differences in the mixed lymphocyte culture. The humoral response to the H-2.2 alloantigen was shown to be controlled by two interacting genes localized within the H-2 complex. Thus, F1 hybrids prepared between parental low responder strains could yield high level immune responses. In addition, strains bearing recombinant H- 2 haplotypes were used to map the two distinct genes controlling the immune response. The alleles at each locus were shown to be highly polymorphic as evidenced by the asymmetric complementation patterns observed. The restricted interactions of specific alleles was termed coupled complementation. The significance of the results in the terms of mechanisms of Ir gene control are discussed.
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spelling pubmed-21807812008-04-17 Coupled complementation of immune response genes controlling responsiveness to the H-2.2 alloantigen J Exp Med Articles The ability of various B10 congenic resistant strains to respond to the alloantigen H-2.2 was tested. High and low antibody-producing strains were distinguished by their anti-H-2.2 hemagglutinating respones. However, these strains do not differ in their ability to respond to these antigenic differences in the mixed lymphocyte culture. The humoral response to the H-2.2 alloantigen was shown to be controlled by two interacting genes localized within the H-2 complex. Thus, F1 hybrids prepared between parental low responder strains could yield high level immune responses. In addition, strains bearing recombinant H- 2 haplotypes were used to map the two distinct genes controlling the immune response. The alleles at each locus were shown to be highly polymorphic as evidenced by the asymmetric complementation patterns observed. The restricted interactions of specific alleles was termed coupled complementation. The significance of the results in the terms of mechanisms of Ir gene control are discussed. The Rockefeller University Press 1977-08-01 /pmc/articles/PMC2180781/ /pubmed/141489 Text en 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 Articles
Coupled complementation of immune response genes controlling responsiveness to the H-2.2 alloantigen
title Coupled complementation of immune response genes controlling responsiveness to the H-2.2 alloantigen
title_full Coupled complementation of immune response genes controlling responsiveness to the H-2.2 alloantigen
title_fullStr Coupled complementation of immune response genes controlling responsiveness to the H-2.2 alloantigen
title_full_unstemmed Coupled complementation of immune response genes controlling responsiveness to the H-2.2 alloantigen
title_short Coupled complementation of immune response genes controlling responsiveness to the H-2.2 alloantigen
title_sort coupled complementation of immune response genes controlling responsiveness to the h-2.2 alloantigen
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2180781/
https://www.ncbi.nlm.nih.gov/pubmed/141489