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ABPC 48 cross-reactive idiotopes in BALB/c mice. Natural and levan- induced expression

Using monoclonal antiidiotypic antibodies, we developed a sensitive binding assay that detects molecules with one or with two idiotopes of the ABPC48 idiotype. ABPC48 cross-reactive idiotypes were thus shown to be present in substantial amounts in sera of nonimmunized mice. Levan binding sites are f...

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Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1983
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2187107/
https://www.ncbi.nlm.nih.gov/pubmed/6886629
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description Using monoclonal antiidiotypic antibodies, we developed a sensitive binding assay that detects molecules with one or with two idiotopes of the ABPC48 idiotype. ABPC48 cross-reactive idiotypes were thus shown to be present in substantial amounts in sera of nonimmunized mice. Levan binding sites are found on these idiotypes. During the life time of the mice, the natural anti-levan titer increases while ABPC48 idiotypic expression remains constant, suggesting different controls for these two activities. On the other hand, ABPC48 cross-reactive idiotypes participate--as minor components--in the response that follows a deliberate immunization with bacterial levan. This induction process is likely to reflect the selection of idiotopes expressed by the B cell clones preactivated in sera of nonimmunized mice rather than the activation of silent clones. We suggest that a similar situation might explain the reported emergence of ABPC48 idiotypes in animals primed with antiidiotypic antibodies and subsequently stimulated with levan.
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spelling pubmed-21871072008-04-17 ABPC 48 cross-reactive idiotopes in BALB/c mice. Natural and levan- induced expression J Exp Med Articles Using monoclonal antiidiotypic antibodies, we developed a sensitive binding assay that detects molecules with one or with two idiotopes of the ABPC48 idiotype. ABPC48 cross-reactive idiotypes were thus shown to be present in substantial amounts in sera of nonimmunized mice. Levan binding sites are found on these idiotypes. During the life time of the mice, the natural anti-levan titer increases while ABPC48 idiotypic expression remains constant, suggesting different controls for these two activities. On the other hand, ABPC48 cross-reactive idiotypes participate--as minor components--in the response that follows a deliberate immunization with bacterial levan. This induction process is likely to reflect the selection of idiotopes expressed by the B cell clones preactivated in sera of nonimmunized mice rather than the activation of silent clones. We suggest that a similar situation might explain the reported emergence of ABPC48 idiotypes in animals primed with antiidiotypic antibodies and subsequently stimulated with levan. The Rockefeller University Press 1983-09-01 /pmc/articles/PMC2187107/ /pubmed/6886629 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
ABPC 48 cross-reactive idiotopes in BALB/c mice. Natural and levan- induced expression
title ABPC 48 cross-reactive idiotopes in BALB/c mice. Natural and levan- induced expression
title_full ABPC 48 cross-reactive idiotopes in BALB/c mice. Natural and levan- induced expression
title_fullStr ABPC 48 cross-reactive idiotopes in BALB/c mice. Natural and levan- induced expression
title_full_unstemmed ABPC 48 cross-reactive idiotopes in BALB/c mice. Natural and levan- induced expression
title_short ABPC 48 cross-reactive idiotopes in BALB/c mice. Natural and levan- induced expression
title_sort abpc 48 cross-reactive idiotopes in balb/c mice. natural and levan- induced expression
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2187107/
https://www.ncbi.nlm.nih.gov/pubmed/6886629