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Association of host immunoglobulins with solid tumours in vivo.

Using a direct radioimmune antiglobulin technique and a competitive double-antibody radioimmune assay, we have demonstrated the presence of appreciable amounts of host immunoglobulins on the surface and in extracts of cell suspensions from freshly excised solid tumours. IgA appeared to have the grea...

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Detalles Bibliográficos
Autores principales: James, K., Bessos, Y. H., Merriman, J.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1979
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2010121/
https://www.ncbi.nlm.nih.gov/pubmed/315785
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author James, K.
Bessos, Y. H.
Merriman, J.
author_facet James, K.
Bessos, Y. H.
Merriman, J.
author_sort James, K.
collection PubMed
description Using a direct radioimmune antiglobulin technique and a competitive double-antibody radioimmune assay, we have demonstrated the presence of appreciable amounts of host immunoglobulins on the surface and in extracts of cell suspensions from freshly excised solid tumours. IgA appeared to have the greatest concentrations from freshly excised solid tumours. IgA appeared to have the greatest concentration, followed in turn by IgM congruent to IgG2a greater than IgG1 congruent to IgG2b greater than IgG3. The amount of immunoglobulin appeared to be influenced by the tumour under investigation and its mode of maintenance. It could also be increased by the administration of C. parvum but was not significantly influenced by the T-cell status of the host.
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spelling pubmed-20101212009-09-10 Association of host immunoglobulins with solid tumours in vivo. James, K. Bessos, Y. H. Merriman, J. Br J Cancer Research Article Using a direct radioimmune antiglobulin technique and a competitive double-antibody radioimmune assay, we have demonstrated the presence of appreciable amounts of host immunoglobulins on the surface and in extracts of cell suspensions from freshly excised solid tumours. IgA appeared to have the greatest concentrations from freshly excised solid tumours. IgA appeared to have the greatest concentration, followed in turn by IgM congruent to IgG2a greater than IgG1 congruent to IgG2b greater than IgG3. The amount of immunoglobulin appeared to be influenced by the tumour under investigation and its mode of maintenance. It could also be increased by the administration of C. parvum but was not significantly influenced by the T-cell status of the host. Nature Publishing Group 1979-11 /pmc/articles/PMC2010121/ /pubmed/315785 Text en https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Research Article
James, K.
Bessos, Y. H.
Merriman, J.
Association of host immunoglobulins with solid tumours in vivo.
title Association of host immunoglobulins with solid tumours in vivo.
title_full Association of host immunoglobulins with solid tumours in vivo.
title_fullStr Association of host immunoglobulins with solid tumours in vivo.
title_full_unstemmed Association of host immunoglobulins with solid tumours in vivo.
title_short Association of host immunoglobulins with solid tumours in vivo.
title_sort association of host immunoglobulins with solid tumours in vivo.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2010121/
https://www.ncbi.nlm.nih.gov/pubmed/315785
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