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      Ablation of CD8 and CD4 T cell responses by high viral loads.

      The Journal of Immunology Author Choice

      Animals, immunology, Virus Activation, Viral Load, biosynthesis, Tumor Necrosis Factor-alpha, secretion, metabolism, Serine Endopeptidases, Pore Forming Cytotoxic Proteins, Perforin, Mice, Knockout, Mice, Inbred DBA, Mice, Inbred C57BL, Mice, genetics, deficiency, Membrane Glycoproteins, Male, Lymphocytic choriomeningitis virus, virology, Lymphocytic Choriomeningitis, Interleukin-2, Interferon-gamma, Granzymes, Gene Rearrangement, beta-Chain T-Cell Antigen Receptor, Female, Epitopes, T-Lymphocyte, Enzyme Activation, Down-Regulation, Clonal Anergy, Cells, Cultured, CD8-Positive T-Lymphocytes, CD4-Positive T-Lymphocytes

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          To evaluate the impact of sustained viral loads on anti-viral T cell responses we compared responses that cleared acute lymphocytic choriomeningitis virus infection with those that were elicited but could not resolve chronic infection. During acute infection, as replicating virus was cleared, CD8 T cell responses were down-regulated, and a pool of resting memory cells developed. In chronically infected hosts, the failure to control the infection was associated with pronounced and prolonged activation of virus-specific CD8 T cells. Nevertheless, there was a progressive diminution of their effector activities as their capacity to produce first IL-2, then TNF-alpha, and finally IFN-gamma was lost. Chronic lymphocytic choriomeningitis virus infection was also associated with differential contraction of certain CD8 T cell responses, resulting in altered immunodominance. However, this altered immunodominance was not due to selective expansion of T cells expressing particular TCR Vbeta segments during chronic infection. High viral loads were not only associated with the ablation of CD8 T cell responses, but also with impaired production of IL-2 by virus-specific CD4 T cells. Taken together, our data show that sustained exposure to high viral loads results in the progressive functional inactivation of virus-specific T cell responses, which may further promote virus persistence.

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