An analysis of the events involved in the differentiation of naive CD8+T cells during a primary immune response in vivo

An analysis of the events involved in the differentiation of naive CD8+T cells during a primary immune response in vivo

Bibliografiska uppgifter
Huvudupphovsmän:	Chiu, C, Bangham, C, Mcmichael, A, Callan, M
Materialtyp:	Conference item
Publicerad:	2005

Liknande verk

Early acquisition of cytolytic function and transcriptional changes in a primary CD8+ T-cell response in vivo.
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CD8(+) T-cell selection, function, and death in the primary immune response in vivo.
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Direct visualization of antigen-specific CD8+ T cells during the primary immune response to Epstein-Barr virus In vivo.
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Human naive CD8 T cells down-regulate expression of the WNT pathway transcription factors lymphoid enhancer binding factor 1 and transcription factor 7 (T cell factor-1) following antigen encounter in vitro and in vivo.
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T cell selection during the evolution of CD8+ T cell memory in vivo.
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Naïve Primary Mouse CD8+ T Cells Retain In Vivo Immune Responsiveness After Electroporation-Based CRISPR/Cas9 Genetic Engineering
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CD45-mediated control of TCR tuning in naïve and memory CD8+ T cells
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BM-MSCs delay the senescence of naive CD8+T cells
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Differentiation of subsets of CD4+ and CD8+ T cells - Discussion
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A single-chain H-2Db molecule presenting an influenza virus nucleoprotein epitope shows enhanced ability at stimulating CD8+ T cell responses in vivo.
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Altered primary CD8+ T cell response to a modified virus Ankara(MVA)-vectored vaccine in the absence of CD4+ T cell help.
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Vaccine route, dose and type of delivery vector determine patterns of primary CD8+ T cell responses.
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Cell Cycle Entry Control in Naïve and Memory CD8+ T Cells
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Primary culture of immature, naïve mouse CD4+ T cells
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Distribution of naive and memory/effector CD4+ T lymphocytes and expression of CD38 on CD8+ T lymphocytes in AIDS patients with tuberculosis
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Sepsis leads to lasting changes in phenotype and function of naïve CD8 T cells.
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Human 'memory' CD4+ T cells are distributed between five phenotypically and functionally distinct subsets.
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Human CD4+ T cells are predominantly distributed among six phenotypically and functionally distinct subsets.
av: Amyes, E, et al.
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