Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Accept all cookies' we'll assume that you are happy to receive all cookies and you won't see this message again. If you click 'Reject all non-essential cookies' only necessary cookies providing core functionality such as security, network management, and accessibility will be enabled. Click 'Find out more' for information on how to change your cookie settings.

Influenza nucleoprotein (NP)-specific T-cell receptor transgenic mice (F5) were crossed with transgenic mice expressing the cognate antigenic protein under the control of the H-2Kb promoter. Double-transgenic mice show negative selection of thymocytes at the CD4+8+TCRlo to CD4+8+TCRhi transition stage. A few CD8+ T cells, however, escape clonal deletion, and in the peripheral lymphoid organs of these mice, they exhibit low levels of the transgenic receptor and upregulated levels of the CD44 memory marker. Such cells do not proliferate upon exposure to antigen stimulation in vivo or ex vivo, however, they can develop low but detectable levels of antigen-specific cytotoxic function after stimulation in vitro in the presence of IL-2.

Original publication

DOI

10.1155/1995/54219

Type

Journal article

Journal

Dev Immunol

Publication Date

1996

Volume

4

Pages

299 - 315

Keywords

Animals, Antigen Presentation, CD4 Antigens, CD8 Antigens, Cytotoxicity, Immunologic, Flow Cytometry, Gene Expression, Hyaluronan Receptors, Immune Tolerance, Lymph Nodes, Mice, Mice, Inbred C57BL, Mice, Transgenic, Nucleoproteins, RNA-Binding Proteins, Receptors, Antigen, T-Cell, T-Lymphocytes, Thymus Gland, Viral Core Proteins