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      Interplay between alpha/beta and gamma interferons with B, T, and natural killer cells in the defense against herpes simplex virus type 1.

      Journal of Biology
      Animals, B-Lymphocytes, immunology, Central Nervous System Infections, virology, DNA, Viral, isolation & purification, Herpes Simplex, Herpesvirus 1, Human, pathogenicity, Interferons, physiology, Killer Cells, Natural, Lymphocyte Subsets, Membrane Proteins, Mice, Mice, Congenic, Mice, Inbred C57BL, Mice, Knockout, Receptor, Interferon alpha-beta, Receptors, Interferon, deficiency, genetics, T-Lymphocytes

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          Abstract

          The essential components of the immune system that control primary and chronic infection with herpes simplex virus type 1 (HSV-1) in mice were investigated. Infection within the first few days can be controlled by alpha/beta interferon (IFN-alpha/beta) alone without significant contribution of B, T, or NK cells. IFN-alpha/beta and IFN-gamma cooperate in the elimination of virus in the absence of these lymphocytes. In contrast, B, T, or NK cells appear to be required to control persistent infection with HSV-1. These results suggest that distinct and essential immune elements are recruited in a time-dependent fashion to control acute and persistent HSV-1 infection.

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