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SPECIFIC IMMUNE RESPONSE GENES OF THE GUINEA PIG : V. INFLUENCE OF THE GA AND GT IMMUNE RESPONSE GENES ON THE SPECIFICITY OF CELLULAR AND HUMORAL IMMUNE RESPONSES TO A TERPOLYMER OFL-GLUTAMIC ACID, L-ALANINE, ANDL-TYROSINE
The ability of guinea pigs to make immune responses to the random linear copolymer of L-glutamic acid and L-alanine, GA, and to L-glutamic acid and L-tyrosine, GT, is each controlled by a different immune response gene. On the other hand, the random linear terpolymer of L-glutamic acid, L-alanine, a...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
1972
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2139119/ https://www.ncbi.nlm.nih.gov/pubmed/5009706 |
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author | Bluestein, Harry G. Green, Ira Maurer, Paul H. Benacerraf, Baruj |
author_facet | Bluestein, Harry G. Green, Ira Maurer, Paul H. Benacerraf, Baruj |
author_sort | Bluestein, Harry G. |
collection | PubMed |
description | The ability of guinea pigs to make immune responses to the random linear copolymer of L-glutamic acid and L-alanine, GA, and to L-glutamic acid and L-tyrosine, GT, is each controlled by a different immune response gene. On the other hand, the random linear terpolymer of L-glutamic acid, L-alanine, and L-tyrosine, GAT, which contains both GA and GT antigenic determinants, is immunogenic in all guinea pigs. After GAT immunization, all animals develop delayed hvpersensitivity and serum antibody specific for GAT. However, only those guinea pigs possessing the GA immune response gene demonstrate cross-reactive delayed hypersensitivity when challenged with GA. In addition, the anti-GAT antisera produced by those animals having the GA gene contain cross-reacting anti-GA antibodies. The sera from guinea pigs lacking the GA gene have no anti-GA antibody activity. Thus, we have demonstrated that a specific immune response gene controlling responsiveness to a "simple" antigen can determine the specificity of both cellular and humoral immune responses to a more complex antigen. |
format | Text |
id | pubmed-2139119 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1972 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21391192008-04-17 SPECIFIC IMMUNE RESPONSE GENES OF THE GUINEA PIG : V. INFLUENCE OF THE GA AND GT IMMUNE RESPONSE GENES ON THE SPECIFICITY OF CELLULAR AND HUMORAL IMMUNE RESPONSES TO A TERPOLYMER OFL-GLUTAMIC ACID, L-ALANINE, ANDL-TYROSINE Bluestein, Harry G. Green, Ira Maurer, Paul H. Benacerraf, Baruj J Exp Med Article The ability of guinea pigs to make immune responses to the random linear copolymer of L-glutamic acid and L-alanine, GA, and to L-glutamic acid and L-tyrosine, GT, is each controlled by a different immune response gene. On the other hand, the random linear terpolymer of L-glutamic acid, L-alanine, and L-tyrosine, GAT, which contains both GA and GT antigenic determinants, is immunogenic in all guinea pigs. After GAT immunization, all animals develop delayed hvpersensitivity and serum antibody specific for GAT. However, only those guinea pigs possessing the GA immune response gene demonstrate cross-reactive delayed hypersensitivity when challenged with GA. In addition, the anti-GAT antisera produced by those animals having the GA gene contain cross-reacting anti-GA antibodies. The sera from guinea pigs lacking the GA gene have no anti-GA antibody activity. Thus, we have demonstrated that a specific immune response gene controlling responsiveness to a "simple" antigen can determine the specificity of both cellular and humoral immune responses to a more complex antigen. The Rockefeller University Press 1972-01-01 /pmc/articles/PMC2139119/ /pubmed/5009706 Text en Copyright © 1972 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 Bluestein, Harry G. Green, Ira Maurer, Paul H. Benacerraf, Baruj SPECIFIC IMMUNE RESPONSE GENES OF THE GUINEA PIG : V. INFLUENCE OF THE GA AND GT IMMUNE RESPONSE GENES ON THE SPECIFICITY OF CELLULAR AND HUMORAL IMMUNE RESPONSES TO A TERPOLYMER OFL-GLUTAMIC ACID, L-ALANINE, ANDL-TYROSINE |
title | SPECIFIC IMMUNE RESPONSE GENES OF THE GUINEA PIG : V. INFLUENCE OF THE GA AND GT IMMUNE RESPONSE GENES ON THE SPECIFICITY OF CELLULAR AND HUMORAL IMMUNE RESPONSES TO A TERPOLYMER OFL-GLUTAMIC ACID, L-ALANINE, ANDL-TYROSINE |
title_full | SPECIFIC IMMUNE RESPONSE GENES OF THE GUINEA PIG : V. INFLUENCE OF THE GA AND GT IMMUNE RESPONSE GENES ON THE SPECIFICITY OF CELLULAR AND HUMORAL IMMUNE RESPONSES TO A TERPOLYMER OFL-GLUTAMIC ACID, L-ALANINE, ANDL-TYROSINE |
title_fullStr | SPECIFIC IMMUNE RESPONSE GENES OF THE GUINEA PIG : V. INFLUENCE OF THE GA AND GT IMMUNE RESPONSE GENES ON THE SPECIFICITY OF CELLULAR AND HUMORAL IMMUNE RESPONSES TO A TERPOLYMER OFL-GLUTAMIC ACID, L-ALANINE, ANDL-TYROSINE |
title_full_unstemmed | SPECIFIC IMMUNE RESPONSE GENES OF THE GUINEA PIG : V. INFLUENCE OF THE GA AND GT IMMUNE RESPONSE GENES ON THE SPECIFICITY OF CELLULAR AND HUMORAL IMMUNE RESPONSES TO A TERPOLYMER OFL-GLUTAMIC ACID, L-ALANINE, ANDL-TYROSINE |
title_short | SPECIFIC IMMUNE RESPONSE GENES OF THE GUINEA PIG : V. INFLUENCE OF THE GA AND GT IMMUNE RESPONSE GENES ON THE SPECIFICITY OF CELLULAR AND HUMORAL IMMUNE RESPONSES TO A TERPOLYMER OFL-GLUTAMIC ACID, L-ALANINE, ANDL-TYROSINE |
title_sort | specific immune response genes of the guinea pig : v. influence of the ga and gt immune response genes on the specificity of cellular and humoral immune responses to a terpolymer ofl-glutamic acid, l-alanine, andl-tyrosine |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2139119/ https://www.ncbi.nlm.nih.gov/pubmed/5009706 |
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