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An immunoglobulin E-dependent recombinant histamine-releasing factor induces interleukin-4 secretion from human basophils

A novel recombinant histamine-releasing factor (rHFR), which stimulates secretion from a subpopulation of human basophils that express a particular type of immunoglobulin E (IgE) or IgE+, was found to induce interleukin-4 (IL-4) production from cells isolated from these same donors. The secretion of...

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Detalles Bibliográficos
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1996
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2192336/
https://www.ncbi.nlm.nih.gov/pubmed/8642270
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description A novel recombinant histamine-releasing factor (rHFR), which stimulates secretion from a subpopulation of human basophils that express a particular type of immunoglobulin E (IgE) or IgE+, was found to induce interleukin-4 (IL-4) production from cells isolated from these same donors. The secretion of IL-4 protein induced by rHRF significantly correlated with histamine release and the amount of protein generated, and the kinetics were identical to those caused by anti-IgE activation. Furthermore, the ability of rHRF to induce IL-4 protein production from cells not normally responsive to this protein was transferred by passive sensitization with plasma containing IgE+ antibody. That this novel protein stimulates both mediator release and the secretion of IL- 4 protein from human basophils suggests a prominent role for this molecule in allergic disease.
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spelling pubmed-21923362008-04-16 An immunoglobulin E-dependent recombinant histamine-releasing factor induces interleukin-4 secretion from human basophils J Exp Med Articles A novel recombinant histamine-releasing factor (rHFR), which stimulates secretion from a subpopulation of human basophils that express a particular type of immunoglobulin E (IgE) or IgE+, was found to induce interleukin-4 (IL-4) production from cells isolated from these same donors. The secretion of IL-4 protein induced by rHRF significantly correlated with histamine release and the amount of protein generated, and the kinetics were identical to those caused by anti-IgE activation. Furthermore, the ability of rHRF to induce IL-4 protein production from cells not normally responsive to this protein was transferred by passive sensitization with plasma containing IgE+ antibody. That this novel protein stimulates both mediator release and the secretion of IL- 4 protein from human basophils suggests a prominent role for this molecule in allergic disease. The Rockefeller University Press 1996-03-01 /pmc/articles/PMC2192336/ /pubmed/8642270 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
An immunoglobulin E-dependent recombinant histamine-releasing factor induces interleukin-4 secretion from human basophils
title An immunoglobulin E-dependent recombinant histamine-releasing factor induces interleukin-4 secretion from human basophils
title_full An immunoglobulin E-dependent recombinant histamine-releasing factor induces interleukin-4 secretion from human basophils
title_fullStr An immunoglobulin E-dependent recombinant histamine-releasing factor induces interleukin-4 secretion from human basophils
title_full_unstemmed An immunoglobulin E-dependent recombinant histamine-releasing factor induces interleukin-4 secretion from human basophils
title_short An immunoglobulin E-dependent recombinant histamine-releasing factor induces interleukin-4 secretion from human basophils
title_sort immunoglobulin e-dependent recombinant histamine-releasing factor induces interleukin-4 secretion from human basophils
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2192336/
https://www.ncbi.nlm.nih.gov/pubmed/8642270