Cargando…

THE ENHANCEMENT OF 19S ANTIBODY PRODUCTION BY PARTICULATE ANTIGEN

Injection of human thyroglobulin solution into rabbits gave rise to a transient 19S antibody response which could however be maintained by repeated administration of antigen. When the antigen was coated onto acrylic resin particles, the titre of 19S antibodies was increased nearly 20-fold whereas 7S...

Descripción completa

Detalles Bibliográficos
Autores principales: Torrigiani, G., Roitt, I. M.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1965
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2138032/
https://www.ncbi.nlm.nih.gov/pubmed/14325470
_version_ 1782143468315869184
author Torrigiani, G.
Roitt, I. M.
author_facet Torrigiani, G.
Roitt, I. M.
author_sort Torrigiani, G.
collection PubMed
description Injection of human thyroglobulin solution into rabbits gave rise to a transient 19S antibody response which could however be maintained by repeated administration of antigen. When the antigen was coated onto acrylic resin particles, the titre of 19S antibodies was increased nearly 20-fold whereas 7S antibody levels were unchanged. This selective enhancement of 19S antibody synthesis by particulate antigen was also seen using human γ-globulin. "Intermediate" sedimenting and 7S γ(1)-antibodies were also increased in animals given particulate antigen. These phenomena may be due to prolonged persistence of the antigen in appropriate macrophages or perhaps to an increased uptake into these cells. The results are discussed in terms of the relationship between 19S and 7S globulin-producing cells.
format Text
id pubmed-2138032
institution National Center for Biotechnology Information
language English
publishDate 1965
publisher The Rockefeller University Press
record_format MEDLINE/PubMed
spelling pubmed-21380322008-04-17 THE ENHANCEMENT OF 19S ANTIBODY PRODUCTION BY PARTICULATE ANTIGEN Torrigiani, G. Roitt, I. M. J Exp Med Article Injection of human thyroglobulin solution into rabbits gave rise to a transient 19S antibody response which could however be maintained by repeated administration of antigen. When the antigen was coated onto acrylic resin particles, the titre of 19S antibodies was increased nearly 20-fold whereas 7S antibody levels were unchanged. This selective enhancement of 19S antibody synthesis by particulate antigen was also seen using human γ-globulin. "Intermediate" sedimenting and 7S γ(1)-antibodies were also increased in animals given particulate antigen. These phenomena may be due to prolonged persistence of the antigen in appropriate macrophages or perhaps to an increased uptake into these cells. The results are discussed in terms of the relationship between 19S and 7S globulin-producing cells. The Rockefeller University Press 1965-07-01 /pmc/articles/PMC2138032/ /pubmed/14325470 Text en Copyright © 1965 by The Rockefeller Institute 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 Article
Torrigiani, G.
Roitt, I. M.
THE ENHANCEMENT OF 19S ANTIBODY PRODUCTION BY PARTICULATE ANTIGEN
title THE ENHANCEMENT OF 19S ANTIBODY PRODUCTION BY PARTICULATE ANTIGEN
title_full THE ENHANCEMENT OF 19S ANTIBODY PRODUCTION BY PARTICULATE ANTIGEN
title_fullStr THE ENHANCEMENT OF 19S ANTIBODY PRODUCTION BY PARTICULATE ANTIGEN
title_full_unstemmed THE ENHANCEMENT OF 19S ANTIBODY PRODUCTION BY PARTICULATE ANTIGEN
title_short THE ENHANCEMENT OF 19S ANTIBODY PRODUCTION BY PARTICULATE ANTIGEN
title_sort enhancement of 19s antibody production by particulate antigen
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2138032/
https://www.ncbi.nlm.nih.gov/pubmed/14325470
work_keys_str_mv AT torrigianig theenhancementof19santibodyproductionbyparticulateantigen
AT roittim theenhancementof19santibodyproductionbyparticulateantigen
AT torrigianig enhancementof19santibodyproductionbyparticulateantigen
AT roittim enhancementof19santibodyproductionbyparticulateantigen