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Differential release of tumor necrosis factor‐α from murine peritoneal macrophages stimulated with virulent and avirulent species of mycobacteria
Author(s) -
Falcone Valeria,
Bassey Effiong B.,
Toniolo Antonio,
Conaldi Pier Giulio,
Collins Frank M.
Publication year - 1994
Publication title -
fems immunology & medical microbiology
Language(s) - English
Resource type - Journals
eISSN - 1574-695X
pISSN - 0928-8244
DOI - 10.1111/j.1574-695x.1994.tb00447.x
Subject(s) - tumor necrosis factor alpha , biology , microbiology and biotechnology , virulence , macrophage , secretion , mycobacterium bovis , mycobacterium tuberculosis , immunology , tuberculosis , in vitro , medicine , pathology , biochemistry , gene
Abstract The ability of Mycobacterium tuberculosis H37Rv and H37Ra, M. bovis BCG and M. smegmatis to induce the secretion of tumor necrosis factor‐α (TNF‐α) by cultured murine peritoneal macrophages is inversely related to their virulence. The avirulent species of mycobacteria which were unable to persist in macrophages were capable of inducing significant levels of TNF‐α compared to that formed in cultures infected with the virulent M. tuberculosis H37Rv. This difference was also associated with an inherent toxicity by live H37Rv for macrophage cultures. Heat‐killed H37Rv was non‐toxic and induced significant levels of TNF‐α; in contrast, live and heat‐killed suspensions of avirulent mycobacteria had an equivalent ability to trigger TNF‐α secretion. The TNF‐α response was dose‐dependent, related directly to the percentage of infected cells, and peaked 6–12 h post‐infection. An early and vigorous TNF‐α response appears to be a marker of macrophage resistance, while the downregulation of this response seems associated with macrophage toxicity and unrestricted mycobacterial growth.

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