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Immunotherapy with mannan-MUC1 and IL-12 in MUC1 transgenic mice

Identifieur interne : 001F30 ( Istex/Checkpoint ); précédent : 001F29; suivant : 001F31

Immunotherapy with mannan-MUC1 and IL-12 in MUC1 transgenic mice

Auteurs : Catherine J. Lees [Australie] ; Vasso Apostolopoulos [Australie] ; Bruce Acres [France] ; Ian Ramshaw [Australie] ; Alistair Ramsay [Australie] ; Chin.-Swee Ong [Australie] ; Ian F. C Mckenzie [Australie]

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RBID : ISTEX:0436D241201D03E24ACFA04DF57DB24A63713B39

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English descriptors

Abstract

Abstract: Mice immunised with oxidised mannan-MUC1 fusion protein (M-FP) develop MHC restricted CD8+ cytotoxic T cells. We now demonstrate that in MUC1/HLA-A2 transgenic mice, IL-12 gives enhanced CTL, CTLp and tumor protection. CTLp in MUC1 transgenic mice with M-FP were 1/55,000, and with IL-12, this increased to 1/19,000, with improved tumor protection. Thus, IL-12 is important for effective CTL responses to MUC1 in transgenic mice.

Url:
DOI: 10.1016/S0264-410X(00)00065-7


Affiliations:


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ISTEX:0436D241201D03E24ACFA04DF57DB24A63713B39

Le document en format XML

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<div type="abstract" xml:lang="en">Abstract: Mice immunised with oxidised mannan-MUC1 fusion protein (M-FP) develop MHC restricted CD8+ cytotoxic T cells. We now demonstrate that in MUC1/HLA-A2 transgenic mice, IL-12 gives enhanced CTL, CTLp and tumor protection. CTLp in MUC1 transgenic mice with M-FP were 1/55,000, and with IL-12, this increased to 1/19,000, with improved tumor protection. Thus, IL-12 is important for effective CTL responses to MUC1 in transgenic mice.</div>
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