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Efficient and selective presentation of antigen-antibody complexes by rheumatoid factor B cells
Using Epstein-Barr virus B cell clones and antigen-specific T cell clones, we asked how antigen-antibody complexes are handled by B cells. We found that the only B cells capable of efficient presentation of antigen-antibody complexes are those that bind the complexes via membrane immunoglobulin, i.e...
Formato: | Texto |
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Lenguaje: | English |
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The Rockefeller University Press
1991
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2118796/ https://www.ncbi.nlm.nih.gov/pubmed/1703209 |
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collection | PubMed |
description | Using Epstein-Barr virus B cell clones and antigen-specific T cell clones, we asked how antigen-antibody complexes are handled by B cells. We found that the only B cells capable of efficient presentation of antigen-antibody complexes are those that bind the complexes via membrane immunoglobulin, i.e., rheumatoid factor-producing B cells and, to a lower extent, antigen-specific B cells. On the contrary, nonspecific B cells, although capable of binding antigen-antibody complexes, fail to present them to T cells. Thus, rheumatoid factor B cells can present any antigen in the context of an immune complex and be triggered by T cells specific for a variety of foreign antigens. These results demonstrate a mechanism of intermolecular help that may be responsible for the production of rheumatoid factor and possibly of other types of autoantibodies. |
format | Text |
id | pubmed-2118796 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1991 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21187962008-04-17 Efficient and selective presentation of antigen-antibody complexes by rheumatoid factor B cells J Exp Med Articles Using Epstein-Barr virus B cell clones and antigen-specific T cell clones, we asked how antigen-antibody complexes are handled by B cells. We found that the only B cells capable of efficient presentation of antigen-antibody complexes are those that bind the complexes via membrane immunoglobulin, i.e., rheumatoid factor-producing B cells and, to a lower extent, antigen-specific B cells. On the contrary, nonspecific B cells, although capable of binding antigen-antibody complexes, fail to present them to T cells. Thus, rheumatoid factor B cells can present any antigen in the context of an immune complex and be triggered by T cells specific for a variety of foreign antigens. These results demonstrate a mechanism of intermolecular help that may be responsible for the production of rheumatoid factor and possibly of other types of autoantibodies. The Rockefeller University Press 1991-02-01 /pmc/articles/PMC2118796/ /pubmed/1703209 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 Efficient and selective presentation of antigen-antibody complexes by rheumatoid factor B cells |
title | Efficient and selective presentation of antigen-antibody complexes by rheumatoid factor B cells |
title_full | Efficient and selective presentation of antigen-antibody complexes by rheumatoid factor B cells |
title_fullStr | Efficient and selective presentation of antigen-antibody complexes by rheumatoid factor B cells |
title_full_unstemmed | Efficient and selective presentation of antigen-antibody complexes by rheumatoid factor B cells |
title_short | Efficient and selective presentation of antigen-antibody complexes by rheumatoid factor B cells |
title_sort | efficient and selective presentation of antigen-antibody complexes by rheumatoid factor b cells |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2118796/ https://www.ncbi.nlm.nih.gov/pubmed/1703209 |