Herpes simplex virus-induced suppression of macrophage-mediated tumoricidal activity in murine macrophages

Herpes simplex virus (HSV) infections can enhance the progression of neoplastic diseases. Since macrophages can be activated to become tumorilytic and may figure prominently in host defense against cancer, the ability of HSV to modify macrophage-mediated tumoricidal functions was evaluated. Murine p...

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Bibliographic Details
Published in:Cancer research (Chicago, Ill.) Ill.), 1987-03, Vol.47 (6), p.1534-1537
Main Authors: KOFF, W. C, DUNEGAN, M. A, CHAKRABARTY, M. K, HAMPAR, B, SHOWALTER, S. D
Format: Article
Language:English
Subjects:
Animals
Applied sciences
Cytotoxicity, Immunologic
Exact sciences and technology
Immune Tolerance
Interferons - pharmacology
Macrophage Activation
Macrophages - immunology
Male
Mice
Mice, Inbred C3H
Mice, Inbred C57BL
Neoplasms, Experimental - immunology
Other techniques and industries
Simplexvirus - immunology
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Summary:Herpes simplex virus (HSV) infections can enhance the progression of neoplastic diseases. Since macrophages can be activated to become tumorilytic and may figure prominently in host defense against cancer, the ability of HSV to modify macrophage-mediated tumoricidal functions was evaluated. Murine peritoneal macrophages treated with HSV could not be activated to a tumoricidal state by mouse recombinant gamma-interferon (IFN-gamma). Addition of HSV 4 h after treatment with IFN-gamma, at a time when the macrophages are fully committed to developing the cytotoxic phenotype, blocked macrophage-mediated lysis of syngeneic melanoma target cells. This inhibition of activation and cytotoxicity was not due simply to uptake of virus particles, because treatment with heat-inactivated HSV at 4-h posttreatment with IFN-gamma had no effect. In addition, HSV did not undergo a productive infection within macrophages, suggesting that the observed inhibitory activity might be due to a virus-induced product. In this regard, treatment of macrophages with recombinant alpha-interferon suppressed the activation of these cells by IFN-gamma, suggesting that virus-induced alpha-interferon may be mediating all or part of the suppressive activity. These studies suggest that enhancement of tumor progression following HSV infection may be related to the virus-induced suppression of macrophage-mediated tumoricidal activity.
ISSN:0008-5472
1538-7445