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Type II collagen-induced arthritis in mice. I. Major histocompatibility complex (I region) linkage and antibody correlates
A model of arthritis was established by the injection of type II collagen into mice. Only mice bearing the H-2q haplotype were susceptible to the disease. Susceptibility was further mapped by the use of recombinant strains on the Iq locus. Type II collagen arthritis was observed in the (resistant X...
Formato: | Texto |
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Lenguaje: | English |
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The Rockefeller University Press
1981
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2186443/ https://www.ncbi.nlm.nih.gov/pubmed/6792316 |
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collection | PubMed |
description | A model of arthritis was established by the injection of type II collagen into mice. Only mice bearing the H-2q haplotype were susceptible to the disease. Susceptibility was further mapped by the use of recombinant strains on the Iq locus. Type II collagen arthritis was observed in the (resistant X susceptible) F1 cross. Mice strains were designated high, intermediate, or low responders with respect to the anti-type II antibody levels measured by radioimmunoassay. Arthritis-susceptible strains were all classified as high antibody responders. The clinical and histological appearance of type II collagen arthritis in the mouse indicates that it may be a good animal model for the investigation of various immunogenetic traits in rheumatoid arthritis. |
format | Text |
id | pubmed-2186443 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1981 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21864432008-04-17 Type II collagen-induced arthritis in mice. I. Major histocompatibility complex (I region) linkage and antibody correlates J Exp Med Articles A model of arthritis was established by the injection of type II collagen into mice. Only mice bearing the H-2q haplotype were susceptible to the disease. Susceptibility was further mapped by the use of recombinant strains on the Iq locus. Type II collagen arthritis was observed in the (resistant X susceptible) F1 cross. Mice strains were designated high, intermediate, or low responders with respect to the anti-type II antibody levels measured by radioimmunoassay. Arthritis-susceptible strains were all classified as high antibody responders. The clinical and histological appearance of type II collagen arthritis in the mouse indicates that it may be a good animal model for the investigation of various immunogenetic traits in rheumatoid arthritis. The Rockefeller University Press 1981-09-01 /pmc/articles/PMC2186443/ /pubmed/6792316 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 Type II collagen-induced arthritis in mice. I. Major histocompatibility complex (I region) linkage and antibody correlates |
title | Type II collagen-induced arthritis in mice. I. Major histocompatibility complex (I region) linkage and antibody correlates |
title_full | Type II collagen-induced arthritis in mice. I. Major histocompatibility complex (I region) linkage and antibody correlates |
title_fullStr | Type II collagen-induced arthritis in mice. I. Major histocompatibility complex (I region) linkage and antibody correlates |
title_full_unstemmed | Type II collagen-induced arthritis in mice. I. Major histocompatibility complex (I region) linkage and antibody correlates |
title_short | Type II collagen-induced arthritis in mice. I. Major histocompatibility complex (I region) linkage and antibody correlates |
title_sort | type ii collagen-induced arthritis in mice. i. major histocompatibility complex (i region) linkage and antibody correlates |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2186443/ https://www.ncbi.nlm.nih.gov/pubmed/6792316 |