Abstract
Mycoplasmas (M. gallisepticum, chicken mycoplasmas), in concert with interferon γ (IFNγ), were effective in activating macrophages (Mθ) to be tumoricidal. The Mθ-activating capacity of mycoplasmas was maintained after treatment with heat, 0.1 M NaOH, 1 M HC1, or trypsin. Mθ-activating factor was extracted from mycoplasmas with chloroform/methanol and water (Mf-B). Mf-B was also effective in activating Mθ in the presence of IFNγ. The threshold dose of Mf-B for Mθ of ordinary C3H/He mice and that for those of C3H/HeJ mice, the latter being known to be low responders to bacterial lipopolysaccharide, were actually the same. This seems to indicate that the effectiveness of Mf-B was not attributable to possibly contaminating lipopolysaccharides, and that the pathway of activity of Mf-B is different from that of lipopolysaccharides. Since the Mθ-activating principle was only a very small part of Mf-B, we have not yet succeeded in identifying it, but there was no evidence that it was protein, nucleic acid, sugar, or lipid. The cytotoxicity of Mθ activated by Mf-B plus IFNγ was dependent on l-arginine in the culture, suggesting that arginine metabolites are involved in Mθ cytotoxicity. Mf-B induced a small amount of tumor necrosis factor in Mθ, and this induction was markedly enhanced by IFNγ.
Original language | English |
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Pages (from-to) | 39-44 |
Number of pages | 6 |
Journal | Cancer Immunology Immunotherapy |
Volume | 33 |
Issue number | 1 |
DOIs | |
Publication status | Published - 01-1991 |
Externally published | Yes |
All Science Journal Classification (ASJC) codes
- Immunology and Allergy
- Immunology
- Oncology
- Cancer Research