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THE STIMULATION OF NON-SPECIFIC HOST RESISTANCE TO INFECTION BY CHEMICALLY MODIFIED ENDOTOXIN

An acetylated derivative prepared from Salmonella typhosa O-901 endotoxin has been found to retain the ability to stimulate non-specific host resistance to a variety of bacterial infections. Relative to the parent endotoxin, the derivative has been reduced in the gross in its pyrogenicity to rabbits...

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Detalles Bibliográficos
Autores principales: Sultzer, Barnet M., Freedman, Henry H.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1962
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2137588/
https://www.ncbi.nlm.nih.gov/pubmed/13979233
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author Sultzer, Barnet M.
Freedman, Henry H.
author_facet Sultzer, Barnet M.
Freedman, Henry H.
author_sort Sultzer, Barnet M.
collection PubMed
description An acetylated derivative prepared from Salmonella typhosa O-901 endotoxin has been found to retain the ability to stimulate non-specific host resistance to a variety of bacterial infections. Relative to the parent endotoxin, the derivative has been reduced in the gross in its pyrogenicity to rabbits and lethality to mice. With the use of this chemically modified preparation under a variety of conditions, the direct dissociation of the toxic properties of endotoxin from its protective capacity appears evident. In young male mice, the endotoxin and its derivative produced a leucocytosis but no leucopenia. However, no direct correlation could be found with the level of the peripheral white blood cells and resistance to infection with Escherichia coli. Furthermore, under the conditions employed, passive transfer of early resistance to infection by serum or plasma was not detectable.
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spelling pubmed-21375882008-04-17 THE STIMULATION OF NON-SPECIFIC HOST RESISTANCE TO INFECTION BY CHEMICALLY MODIFIED ENDOTOXIN Sultzer, Barnet M. Freedman, Henry H. J Exp Med Article An acetylated derivative prepared from Salmonella typhosa O-901 endotoxin has been found to retain the ability to stimulate non-specific host resistance to a variety of bacterial infections. Relative to the parent endotoxin, the derivative has been reduced in the gross in its pyrogenicity to rabbits and lethality to mice. With the use of this chemically modified preparation under a variety of conditions, the direct dissociation of the toxic properties of endotoxin from its protective capacity appears evident. In young male mice, the endotoxin and its derivative produced a leucocytosis but no leucopenia. However, no direct correlation could be found with the level of the peripheral white blood cells and resistance to infection with Escherichia coli. Furthermore, under the conditions employed, passive transfer of early resistance to infection by serum or plasma was not detectable. The Rockefeller University Press 1962-11-30 /pmc/articles/PMC2137588/ /pubmed/13979233 Text en ©Copyright, 1962, 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
Sultzer, Barnet M.
Freedman, Henry H.
THE STIMULATION OF NON-SPECIFIC HOST RESISTANCE TO INFECTION BY CHEMICALLY MODIFIED ENDOTOXIN
title THE STIMULATION OF NON-SPECIFIC HOST RESISTANCE TO INFECTION BY CHEMICALLY MODIFIED ENDOTOXIN
title_full THE STIMULATION OF NON-SPECIFIC HOST RESISTANCE TO INFECTION BY CHEMICALLY MODIFIED ENDOTOXIN
title_fullStr THE STIMULATION OF NON-SPECIFIC HOST RESISTANCE TO INFECTION BY CHEMICALLY MODIFIED ENDOTOXIN
title_full_unstemmed THE STIMULATION OF NON-SPECIFIC HOST RESISTANCE TO INFECTION BY CHEMICALLY MODIFIED ENDOTOXIN
title_short THE STIMULATION OF NON-SPECIFIC HOST RESISTANCE TO INFECTION BY CHEMICALLY MODIFIED ENDOTOXIN
title_sort stimulation of non-specific host resistance to infection by chemically modified endotoxin
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2137588/
https://www.ncbi.nlm.nih.gov/pubmed/13979233
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