Inhibition of normal rat macrophage functions by soluble tumor products. Effect of systemic treatment with bacterial immunomodulators
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Abstract:
The phagocytic and chemotactic activities of normal rat peritoneal macrophages were inhibited by sera from tumor-bearing rats (TBR) and 3 M KCl extracts of tumor mass. However, sera from Corynebacterium parvum- or Listeria monocytogenes-treated TBR did not inhibit phagocytosis. On the other hand, sera from C. parvum-treated, but not from L. monocytogenes-treated TBR still inhibited the chemotactic response of the normal macrophages. Furthermore, 3 M KCl extracts of tumors from C. parvum-treated TBR did not inhibit phagocytosis and chemotactic response of the same cells. Similar results were obtained with extracts of tumor masses from L. monocytogenes-treated rats. It is suggested that treatment with bacterial immunomodulators can influence the release from neoplastic cells of soluble products influencing normal macrophage functions.
Insights
Sera from tumor-bearing rats inhibit macrophage functions. Bacterial immunomodulator treatment of tumor-bearing rats partially restored normal macrophage phagocytic and chemotactic activities, suggesting modulation of tumor-derived inhibitory factors.
Area of Science:
- Immunology
- Cancer Biology
- Macrophage Function
Background:
- Tumor-bearing rats (TBR) exhibit sera and tumor extracts that inhibit normal macrophage phagocytosis and chemotaxis.
- Bacterial immunomodulators are known to affect immune responses in cancer models.
Purpose of the Study:
- To investigate the effect of bacterial immunomodulator treatment on the inhibitory properties of TBR sera and tumor extracts on normal rat peritoneal macrophages.
- To determine if immunomodulator treatment alters the release of soluble factors from tumor cells that affect macrophage function.
Main Methods:
- Collection of sera and 3 M KCl tumor extracts from normal rats, TBR, and TBR treated with Corynebacterium parvum or Listeria monocytogenes.
- Assay of phagocytic and chemotactic activities of normal rat peritoneal macrophages incubated with these sera and extracts.
Main Results:
- Sera from untreated TBR inhibited both phagocytosis and chemotaxis.
- Sera from C. parvum- or L. monocytogenes-treated TBR showed reduced inhibition of phagocytosis.
- Sera from C. parvum-treated TBR still inhibited chemotaxis, while L. monocytogenes treatment did not.
- Tumor extracts from immunomodulator-treated TBR did not inhibit macrophage phagocytosis or chemotaxis.
Conclusions:
- Treatment with bacterial immunomodulators can reverse or reduce the inhibitory effects of tumor-derived factors on macrophage functions.
- Immunomodulator therapy may influence the production of soluble suppressive factors by tumor cells, thereby restoring macrophage activity.
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