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      Hydroxyurea exerts an anti-proliferative effect on T cells but has no direct impact on cellular activation.

      Clinical and Experimental Immunology
      Anti-HIV Agents, pharmacology, Antigens, CD, metabolism, Antigens, CD38, Antigens, Differentiation, T-Lymphocyte, Cell Proliferation, drug effects, Cells, Cultured, Dose-Response Relationship, Drug, Humans, Hydroxyurea, Interleukin-2 Receptor alpha Subunit, Lectins, C-Type, Lymphocyte Activation, T-Lymphocytes, immunology

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          Abstract

          Hydroxyurea (HU) is a cytostatic drug which has been used as an anti-HIV agent due mainly to its synergistic activity when combined with certain anti-retrovirals. In addition, HU might have a beneficial effect on parameters involved in the pathogenesis of HIV infection, such as immune activation. To test this hypothesis, the effect of HU on T cell proliferation and T cell activation, as well as the potential association between these two phenomena, were examined in an in vitro model. HU exerted a dose-dependent anti-proliferative effect on T cells, and modulated the expression of different activation markers. In cells exposed to HU, expression of CD25 and CD38 diminished in a dose-dependent manner, whereas expression of CD69 increased. However, when the expression of these markers was examined separately on proliferating and non-proliferating lymphocytes, HU did not exert any significant effect. Thus, the effect of HU on T cell activation is not direct and seems to be mediated through its effect on T cell proliferation.

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