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Expression of Ia antigens on hapten-specific B cells. I. Delineation of B-cell subpopulations
The nonimmune adult spleen contains at least two B-cell subpopulations. The majority of primary B cells express cell surface Ia determinants and have the capacity to give rise to IgG antibody-producing clones after T-cell dependent antigenic stimulation. There is also a small subpopulation of primar...
Formato: | Texto |
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Lenguaje: | English |
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The Rockefeller University Press
1976
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2190390/ https://www.ncbi.nlm.nih.gov/pubmed/1085328 |
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collection | PubMed |
description | The nonimmune adult spleen contains at least two B-cell subpopulations. The majority of primary B cells express cell surface Ia determinants and have the capacity to give rise to IgG antibody-producing clones after T-cell dependent antigenic stimulation. There is also a small subpopulation of primary B cells which are, by definition, Ia negative, since their activity is not eliminated by negative selection with anti- Ia serum and complement. The Ia-negative B cells give rise to clones that produce only IgM antibody. These B-cell subsets may form a continuum in B-cell maturation, or they may exist as discrete B-cell lineages. Since the cellular expression of Ia antigens appears to correlate with the ability of the B cell to generate IgG-producing clones, it is speculated that Ia molecules may have a role in the IgM to IgG B-cell switch mechanism. |
format | Text |
id | pubmed-2190390 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1976 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21903902008-04-17 Expression of Ia antigens on hapten-specific B cells. I. Delineation of B-cell subpopulations J Exp Med Articles The nonimmune adult spleen contains at least two B-cell subpopulations. The majority of primary B cells express cell surface Ia determinants and have the capacity to give rise to IgG antibody-producing clones after T-cell dependent antigenic stimulation. There is also a small subpopulation of primary B cells which are, by definition, Ia negative, since their activity is not eliminated by negative selection with anti- Ia serum and complement. The Ia-negative B cells give rise to clones that produce only IgM antibody. These B-cell subsets may form a continuum in B-cell maturation, or they may exist as discrete B-cell lineages. Since the cellular expression of Ia antigens appears to correlate with the ability of the B cell to generate IgG-producing clones, it is speculated that Ia molecules may have a role in the IgM to IgG B-cell switch mechanism. The Rockefeller University Press 1976-08-01 /pmc/articles/PMC2190390/ /pubmed/1085328 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 Expression of Ia antigens on hapten-specific B cells. I. Delineation of B-cell subpopulations |
title | Expression of Ia antigens on hapten-specific B cells. I. Delineation of B-cell subpopulations |
title_full | Expression of Ia antigens on hapten-specific B cells. I. Delineation of B-cell subpopulations |
title_fullStr | Expression of Ia antigens on hapten-specific B cells. I. Delineation of B-cell subpopulations |
title_full_unstemmed | Expression of Ia antigens on hapten-specific B cells. I. Delineation of B-cell subpopulations |
title_short | Expression of Ia antigens on hapten-specific B cells. I. Delineation of B-cell subpopulations |
title_sort | expression of ia antigens on hapten-specific b cells. i. delineation of b-cell subpopulations |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2190390/ https://www.ncbi.nlm.nih.gov/pubmed/1085328 |