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Subversion of host defense mechanisms by malignant tumors: an established tumor as a privileged site for bacterial growth
Mice carrying any one of three murine tumors in their right hind foot pad were incapable of eliminating an inoculum of the bacterial parasite Listeria monocytogenes from the progressive tumor. In contrast, they were as capable as control mice in efficiently eliminating the organism from their contra...
Formato: | Texto |
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Lenguaje: | English |
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The Rockefeller University Press
1977
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2180651/ https://www.ncbi.nlm.nih.gov/pubmed/404387 |
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collection | PubMed |
description | Mice carrying any one of three murine tumors in their right hind foot pad were incapable of eliminating an inoculum of the bacterial parasite Listeria monocytogenes from the progressive tumor. In contrast, they were as capable as control mice in efficiently eliminating the organism from their contralateral tumor-free foot pad, and from their lymph nodes and livers. The results serve to show, therefore, that conditions within an established tumor are not only antagonistic to the expression of concomitant anti-tumor immunity, but that they are also antagonistic to the expression of T-cell-mediated anti-bacterial immunity. The possibility was discussed that the tumor contains factors that act pharmacologically to locally suppress the function of sensitized T cells and activated macrophages. |
format | Text |
id | pubmed-2180651 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1977 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21806512008-04-17 Subversion of host defense mechanisms by malignant tumors: an established tumor as a privileged site for bacterial growth J Exp Med Articles Mice carrying any one of three murine tumors in their right hind foot pad were incapable of eliminating an inoculum of the bacterial parasite Listeria monocytogenes from the progressive tumor. In contrast, they were as capable as control mice in efficiently eliminating the organism from their contralateral tumor-free foot pad, and from their lymph nodes and livers. The results serve to show, therefore, that conditions within an established tumor are not only antagonistic to the expression of concomitant anti-tumor immunity, but that they are also antagonistic to the expression of T-cell-mediated anti-bacterial immunity. The possibility was discussed that the tumor contains factors that act pharmacologically to locally suppress the function of sensitized T cells and activated macrophages. The Rockefeller University Press 1977-05-01 /pmc/articles/PMC2180651/ /pubmed/404387 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 Subversion of host defense mechanisms by malignant tumors: an established tumor as a privileged site for bacterial growth |
title | Subversion of host defense mechanisms by malignant tumors: an established tumor as a privileged site for bacterial growth |
title_full | Subversion of host defense mechanisms by malignant tumors: an established tumor as a privileged site for bacterial growth |
title_fullStr | Subversion of host defense mechanisms by malignant tumors: an established tumor as a privileged site for bacterial growth |
title_full_unstemmed | Subversion of host defense mechanisms by malignant tumors: an established tumor as a privileged site for bacterial growth |
title_short | Subversion of host defense mechanisms by malignant tumors: an established tumor as a privileged site for bacterial growth |
title_sort | subversion of host defense mechanisms by malignant tumors: an established tumor as a privileged site for bacterial growth |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2180651/ https://www.ncbi.nlm.nih.gov/pubmed/404387 |