Literature DB >> 8812696

Isolation of CD4+ and CD8+ T-Cell Clones from Mice Immunized with Synthetic Peptides on Splenic Dendritic Cells

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Abstract

Splenic dendritic cells (DC) express high levels of MHC, co-stimulator, and adhesion molecules and have been shown to be extremely potent antigen-presenting cells for both CD4(+) and CD8(+) T-cell responses. Previous studies have shown that murine DC can be loaded with exogenous antigens and used to prime CD4(+), Class II-restricted T-cell responses in vivo. This article describes protocols for immunization using DC loaded with peptides bound to Class I or Class II molecules and for the derivation and characterization of CD4(+) and CD8(+) antigen-specific T-cell lines and clones. The rationale for using DC as antigen-presenting cells is discussed, together with the advantages and disadvantages of these cells compared with more conventional methods of immunization.

Entities:  

Year:  1996        PMID: 8812696     DOI: 10.1006/meth.1996.0048

Source DB:  PubMed          Journal:  Methods        ISSN: 1046-2023            Impact factor:   3.608


  3 in total

1.  Genes predisposing to autoimmunity augment constitutive major histocompatibility complex class II-associated presentation of the self-antigen IgG2a in vivo.

Authors:  K Bartnes; X Li; M Iwamoto; S Izui; K Hannestad
Journal:  Immunology       Date:  2000-08       Impact factor: 7.397

2.  Native IgG2a(b) is barely antigenic to major histocompatibility complex class II-restricted T cells owing to inefficient internalization by professional antigen-presenting cells.

Authors:  K Bartnes; K Hannestad
Journal:  Immunology       Date:  2000-04       Impact factor: 7.397

3.  Direct, help-independent priming of CD8+ T cells by adeno-associated virus-transduced hepatocytes.

Authors:  Sherry A Wuensch; Jessica Spahn; Ian N Crispe
Journal:  Hepatology       Date:  2010-09       Impact factor: 17.425

  3 in total

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