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Neonatal treatment with low doses of anti-idiotypic antibody leads to the expression of a silent clone

BALB/c mice immunized with bacterial levan (BL) produce an immune response that fails to generate antibody expressing the idiotype (Id) of the beta (2 leads to 6) fructosan-binding myeloma protein ABPC 48 (A48). Pretreatment of newborn BALB/c mice (at 1 d of age) with 0.01-10 microgram of affinity p...

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Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1981
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2186123/
https://www.ncbi.nlm.nih.gov/pubmed/7019374
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collection PubMed
description BALB/c mice immunized with bacterial levan (BL) produce an immune response that fails to generate antibody expressing the idiotype (Id) of the beta (2 leads to 6) fructosan-binding myeloma protein ABPC 48 (A48). Pretreatment of newborn BALB/c mice (at 1 d of age) with 0.01-10 microgram of affinity purified BALB/c anti-A48 Id antibody followed by immunization with BL 1-2 mo later produces an anti-BL response that expresses the A48 Id. This shows that A48 Id+ anti-BL clones belong to a normally silent fraction of the anti-BL repertoire. The activation of A48 Id+ anti-BL clones anti-A48 Id antibody is specific because the pretreatment of newborn mice with anti-MOPC 384 Id antibody, followed by immunization with BL, does not lead to its activation. Moreover, pretreatment of mice with anti-A48 Id antibody does not alter the MOPC 460 Id+ component of the anti-TNP response. It is also important to note that the activation of the A48 Id+ clone in pretreated mice requires subsequent immunization with BL.
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spelling pubmed-21861232008-04-17 Neonatal treatment with low doses of anti-idiotypic antibody leads to the expression of a silent clone J Exp Med Articles BALB/c mice immunized with bacterial levan (BL) produce an immune response that fails to generate antibody expressing the idiotype (Id) of the beta (2 leads to 6) fructosan-binding myeloma protein ABPC 48 (A48). Pretreatment of newborn BALB/c mice (at 1 d of age) with 0.01-10 microgram of affinity purified BALB/c anti-A48 Id antibody followed by immunization with BL 1-2 mo later produces an anti-BL response that expresses the A48 Id. This shows that A48 Id+ anti-BL clones belong to a normally silent fraction of the anti-BL repertoire. The activation of A48 Id+ anti-BL clones anti-A48 Id antibody is specific because the pretreatment of newborn mice with anti-MOPC 384 Id antibody, followed by immunization with BL, does not lead to its activation. Moreover, pretreatment of mice with anti-A48 Id antibody does not alter the MOPC 460 Id+ component of the anti-TNP response. It is also important to note that the activation of the A48 Id+ clone in pretreated mice requires subsequent immunization with BL. The Rockefeller University Press 1981-04-01 /pmc/articles/PMC2186123/ /pubmed/7019374 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
Neonatal treatment with low doses of anti-idiotypic antibody leads to the expression of a silent clone
title Neonatal treatment with low doses of anti-idiotypic antibody leads to the expression of a silent clone
title_full Neonatal treatment with low doses of anti-idiotypic antibody leads to the expression of a silent clone
title_fullStr Neonatal treatment with low doses of anti-idiotypic antibody leads to the expression of a silent clone
title_full_unstemmed Neonatal treatment with low doses of anti-idiotypic antibody leads to the expression of a silent clone
title_short Neonatal treatment with low doses of anti-idiotypic antibody leads to the expression of a silent clone
title_sort neonatal treatment with low doses of anti-idiotypic antibody leads to the expression of a silent clone
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2186123/
https://www.ncbi.nlm.nih.gov/pubmed/7019374