
pmid: 15105501
Memory T cells are long-lived antigen-experienced T cells that are generally accepted to be direct descendants of proliferating primary effector cells. However, the factors that permit selective survival of these T cells are not well established. We show that homodimeric α chains of the CD8 molecule (CD8αα) are transiently induced on a selected subset of CD8αβ + T cells upon antigenic stimulation. These CD8αα molecules promote the survival and differentiation of activated lymphocytes into memory CD8 T cells. Thus, memory precursors can be identified among primary effector cells and are selected for survival and differentiation by CD8αα.
Mice, Knockout, Membrane Glycoproteins, Receptors, Interleukin-7, Cell Survival, CD8 Antigens, Antigen-Presenting Cells, Cell Differentiation, Mice, Transgenic, CD8-Positive T-Lymphocytes, Lymphocyte Activation, Mice, Inbred C57BL, Interferon-gamma, Mice, T-Lymphocyte Subsets, Animals, Arenaviridae Infections, Lymphocytic choriomeningitis virus, Immunologic Memory
Mice, Knockout, Membrane Glycoproteins, Receptors, Interleukin-7, Cell Survival, CD8 Antigens, Antigen-Presenting Cells, Cell Differentiation, Mice, Transgenic, CD8-Positive T-Lymphocytes, Lymphocyte Activation, Mice, Inbred C57BL, Interferon-gamma, Mice, T-Lymphocyte Subsets, Animals, Arenaviridae Infections, Lymphocytic choriomeningitis virus, Immunologic Memory
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