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Enhanced tumor development in mice lacking a functional type I interferon receptor.

Sandrine Picaud·Boris Bardot·Edward De Maeyer·Isabelle Seif
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Abstract

The aim of this study was to investigate the contribution of endogenous - that is, without the addition of any interferon (IFN) inducer - type I IFN production in the defense against tumor development. To this purpose, the IFN-alpha receptor (IFNAR) knockout (KO)-induced mutation, resulting in the complete absence of IFN-alpha/beta activity, was introduced into a C3H genetic background by 10 backcross generations, followed by brother-sister matings for at least four generations. The resulting mice were inoculated either with syngeneic C3H melanoma K1735 cells, with allogeneic 3LL carcinoma cells, or with allogeneic B16F10 melanoma cells. With all three tumor cell lines, tumor development and ensuing mortality were enhanced in the IFNAR KO animals. This indicates that endogenous IFN-alpha/beta production is a mediator of natural immunity to tumor development.

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AnimalsCarcinoma, Lewis LungCell DivisionFemaleInjections, IntramuscularInjections, SubcutaneousKineticsMaleMelanoma, ExperimentalMembrane ProteinsMiceMice, Inbred C3HMice, KnockoutNeoplasm TransplantationNeoplasms, ExperimentalReceptor, Interferon alpha-betaReceptors, InterferonSurvival RateTumor Cells, CulturedComparative StudyJournal Article

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Sandrine Picaud, Boris Bardot, Edward De Maeyer, Isabelle Seif. 2002. Enhanced tumor development in mice lacking a functional type I interferon receptor.. https://doi.org/10.1089/10799900252952244

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