Increased cell-mediated immune responses in patients with recurrent herpes simplex virus type 2 meningitis

Clin Vaccine Immunol. 2011 Apr;18(4):655-60. doi: 10.1128/CVI.00333-10. Epub 2011 Feb 16.

Abstract

The clinical picture of herpes simplex virus type 2 (HSV-2) infection includes genital blisters and less frequently meningitis, and some individuals suffer from recurrent episodes of these manifestations. We hypothesized that adaptive and/or innate immune functional deficiencies may be a major contributing factor in susceptibility to recurrent HSV-2 meningitis. Ten patients with recurrent HSV-2 meningitis were studied during clinical remission. For comparison, 10 patients with recurrent genital HSV infections as well as 21 HSV-seropositive and 19 HSV-seronegative healthy blood donors were included. HSV-specific T cell blasting and cytokine secretion were evaluated in whole blood cultures. HSV-2-induced NK cell gamma interferon production, dendritic cell Toll-like receptor (TLR) expression, and TLR agonist-induced alpha interferon secretion were analyzed. Patients with recurrent HSV-2 meningitis had elevated T cell blasting and Th1 and Th2 cytokine production in response to HSV antigens compared to those of patients with recurrent genital infections. A somewhat increased NK cell response, increased dendritic cell expression of TLR3 and -9, and increased TLR-induced alpha interferon responses were also noted. Contrary to our expectation, recurrent HSV-2 meningitis patients have increased HSV-specific adaptive and innate immune responses, raising the possibility of immune-mediated pathology in the development of recurrent HSV2 meningitis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Cytokines / metabolism
  • Dendritic Cells / immunology
  • Female
  • Gene Expression
  • Herpes Simplex / immunology*
  • Herpesvirus 2, Human / immunology*
  • Humans
  • Immunity, Cellular*
  • Killer Cells, Natural / immunology
  • Male
  • Meningitis, Viral / immunology*
  • Middle Aged
  • Recurrence
  • T-Lymphocytes / immunology
  • Toll-Like Receptors / immunology

Substances

  • Cytokines
  • Toll-Like Receptors