CD4^+T cell-mediated protection against a lethal outcome of systemic infection with vesicular stomatitis virus requires CD40 ligand expression, but not IFN-γ or IL-4
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概要
- 論文の詳細を見る
- 1999-12-01
著者
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Thomsen A
Univ. Copenhagen Copenhagen Dnk
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Thomsen Allan
Institute Of Medical Microbiology And Immunology Panum Institute University Of Copenhagen
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Andersen Camilla
Institute Of Medical Microbiology And Immunology Panum Institute University Of Copenhagen
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NANSEN Anneline
Institute of Medical Microbiology and Immunology, The Panum Institute, University of Copenhagen
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MARKER Ole
Institute of Medical Microbiology and Immunology, The Panum Institute, University of Copenhagen
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JENSEN Teis
Institute of Medical Microbiology and Immunology, Panum Institute, University of Copenhagen
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Jensen Teis
Institute Of Medical Microbiology And Immunology Panum Institute University Of Copenhagen
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Marker Ole
Institute Of Medical Microbiology And Immunology Panum Institute University Of Copenhagen
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Nansen Anneline
Institute Of Medical Microbiology And Immunology Panum Institute University Of Copenhagen
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Thomsen Allan
Institute Of Medical Microbiology And Immunology Panum Institute
関連論文
- Virus-induced polyclonal T cell activation is followed by apoptosis: partitioning of CD8^+ T cells based on α4 integrin expression
- Effect of the CTL proliferation program on virus dynamics
- Cooperation of B cells and T cells is required for survival of mice infected with vesicular stomatitis virus
- CD4^+T cell-mediated protection against a lethal outcome of systemic infection with vesicular stomatitis virus requires CD40 ligand expression, but not IFN-γ or IL-4
- Virus-induced non-specific signals cause cell cycle progression of primed CD^+ T cells but do not induce cell differentiation
- Characterization of virus-primed CD8^+ T cells with a type 1 cytokine profile
- Role of CD28 co-stimulation in generation and maintenance of virus-specific T cells