## Abstract Cells of a methylcholanthreneβinduced fibrosarcoma, injected intravenously into syngeneic C57Bl mice, generated tumour nodules (βmetastasesβ) in the lungs. The number of tumour nodules was reduced in recipients whose spleens had been previously removed. This effect of splenectomy was sp
The effect of interferon on experimental metastases in immunocompetent and immunodeficient mice
β Scribed by P. Ramani; I. R. Hart; F. R. Balkwill
- Publisher
- John Wiley and Sons
- Year
- 1986
- Tongue
- French
- Weight
- 556 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0020-7136
No coin nor oath required. For personal study only.
β¦ Synopsis
A recombinant human hybrid alpha interferon (rlFN-a AID) with antiviral, immunomodulating and cell-growth-inhibitory activity on murine cells strongly inhibited the development of experimental pulrnonary metastases of the Colo 26 adenocarcinoma in BALBlc mice. Twenty-one days after i.v. injection of 5 x lo4 cells, 8/8 control mice had >200 lung tumour nodules whereas 1/6 mice receiving 500 ng rlFN-a A/ D had one lung tumour nodule and the other 5 mice were tumour-free. Equally strong inhibition was seen in immunodeficient BALBlc nulnu (athymic) and beige nu/nu (athymic and NK-deficient) mice. Scheduling experiments in vivo showed that the most important time of IFN treatment was from the day of tumour cell injection to day 5, although statistically significant reductions in lung tumour nodule number and lung weight were seen even when IFN treatment was started 7 days after cell injection. rlFN-a A/D was cytostatic to Colo 26 in vitro, causing 50% or more inhibition of cell growth or colony number at IFN levels that could be achieved in the sera of IFN-treated mice. Although rlFN-rn AID stimulated NK-cell activity in BALB/c mice, Colo 26 cells were resistant in vitro to such cells whether from control or IFN treated mice.
π SIMILAR VOLUMES
The effect of a human recombinant hybrid alpha interferon (referred to as rHulFN-alphaA/D) on pulmonary metastases induced by intravenous injection of B16 FIO melanoma cells in C57BU6 mice was examined; rHulFN-alphaAID has been previously shown to have anti-viral, anti-proliferative and immunomodula
DBAl2 mice were injected i.v. with IFN alp-resistant 3C I 8 Friend erythroleukemia cells (FLC) which metastasize to the liver and spleen. IFN d p treatment of FLC-injected mice increased their survival time and these mice developed a resistance to a second challenge with FLC. The efficacy of IFN d p