Interleukin-7 promotes CD8 T cell activity in patients with enterovirus 71 associated encephalitis.

Int Immunopharmacol

The First Ward in Department of Neurology, The First Affiliated Hospital of Xinxiang Medical University, Weihui, Xinxiang, Henan Province 453100, PR China.

Published: October 2019

Enterovirus 71 (EV71) always induces severe hand, foot, and mouth disease with neurological complications, such as encephalitis. Interleukin (IL)-7 augments CD8 T cells activity in chronic viral infection and cancers. However, few studies have focused on common γ-chain (γc) cytokine expression and regulatory function of IL-7 to CD8 T cells in EV71 associated encephalitis. In this study, twenty-one patients with EV71 associated encephalitis, twenty-seven patients with febrile convulsion (FC), and twenty healthy individuals were enrolled. γc cytokine (IL-2, IL-4, IL-7 and IL-15) concentration was measured by ELISA. IL-7 receptor α chain (membrane/soluble CD127) expression was also investigated. Purified CD8 T cells were stimulated with recombinant human IL-7 in vitro. The regulatory activity of IL-7 to CD8 T cells from peripheral blood and cerebrospinal fluids (CSF) was investigated in direct and indirect contact co-culture with U-87MG cells. IL-7 in the serum and CSF, but not IL-2, IL-4, or IL-15, was significant increased in EV71 associated encephalitis. Both total CD127 mRNA relative level and membrane/soluble CD127 expression was comparable among three groups. IL-7 stimulation promoted CD8 T cells proliferation, up-regulated perforin/granzyme B level, but reduced programmed death-1 expression in CD8 T cells from EV71 associated encephalitis patients. Cytotoxicity and interferon-γ production of CD8 T cells from peripheral blood and CSF was also augmented in response to IL-7 stimulation in both direct and indirect co-culture systems in EV71 associated encephalitis. The present data indicated that IL-7 induced cytolytic and non-cytolytic functions of CD8 T cells in EV71 associated encephalitis. IL-7 might be considered as one of the immunomodulatory therapeutic candidates for EV71 infection.

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http://dx.doi.org/10.1016/j.intimp.2019.105773DOI Listing

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