Tumor necrosis factor-a in combination with interferon-y , but not with interleukin 4 activates murine macrophages for elimination of Leishmania major amastigotes" We have previously shown that during an infection with Leishmania major, susceptible BALBlc mice, as opposed to mice of a resistant str
Anti-tumor activity of tumor necrosis factor in combination with interferon-γ is not affected by prior tolerization
✍ Scribed by Nozomi Takahashi; Walter Fiers; Peter Brouckaert
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- French
- Weight
- 730 KB
- Volume
- 63
- Category
- Article
- ISSN
- 0020-7136
No coin nor oath required. For personal study only.
✦ Synopsis
Repetitive administration of low doses of tumor necrosis factor (TNF) results in a state of selective tolerance to some of its effects. We have demonstrated that tolerance does not impair the therapeutic efficacy of TNF against a syngeneic murine B I6BL6 melanoma and allows a complete cure. Another study, performed with a distinct tumor model, came to apparently contradictory results. To claritj this, we investigated whether the outcome depended on the tumor type and on the inclusion of interferon-y (IFNy) in the treatment. Three syngeneic tumors of different histological origin, i.e., B I6BL6 melanoma, Lewis lung carcinoma (LLC) and EL4 lymphoma, were compared in C57BLl6 mice. The anti-tumor efficacy of TNF against B I6BL6 and EL4 was not impaired in tolerant mice, but the effect of TNF against LLC was slightly, though significantly, reduced. Inclusion of IFNy in the treatment regimen, however, abolished this difference and resulted in complete cure for all 3 tumor systems. As therapeutically optimal doses were lethal in normal mice, only tolerance allowed a long-term cure. We conclude that the influence of tolerance on the anti-tumor activity of TNF as a single agent depends on the tumor type; in combination therapy with IFNy, however, tolerance allowed us to dissociate lethal toxicity from anti-tumor activity, irrespective of the tumor type tested.
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