IN-VIVO PRODUCTION OF CYTOKINES AND BETA-(C-C) CHEMOKINES IN HUMAN RECURRENT HERPES-SIMPLEX LESIONS - DO HERPES-SIMPLEX VIRUS-INFECTED KERATINOCYTES CONTRIBUTE TO THEIR PRODUCTION
Z. Mikloska et al., IN-VIVO PRODUCTION OF CYTOKINES AND BETA-(C-C) CHEMOKINES IN HUMAN RECURRENT HERPES-SIMPLEX LESIONS - DO HERPES-SIMPLEX VIRUS-INFECTED KERATINOCYTES CONTRIBUTE TO THEIR PRODUCTION, The Journal of infectious diseases, 177(4), 1998, pp. 827-838
Recurrent human herpes simplex lesions are infiltrated by macrophages
and CD4 and CD8 lymphocytes, which secrete cytokines and chemokines. V
esicle fluid was examined by ELISA for the presence of cytokines and b
eta (C-C) chemokines. On the first day of the lesion, high concentrati
ons of interleukin (IL)-1 beta and IL-6, moderate concentrations of IL
-1 alpha and IL-10, and low concentrations of IL-12 and beta chemokine
s were found; levels of macrophage inflammatory protein (MIP)-1 beta w
ere significantly higher than levels of MIP-1 alpha and RANTES. At day
3, the concentrations of IL-1 beta, IL-6, and MIP-1 beta were lower,
whereas the levels of IL-10, IL-12, and MIP-1 alpha remained similar,
and the level of tumor necrosis factor-alpha was now detectable. Herpe
s simplex virus infection of keratinocytes in vitro stimulated product
ion of beta chemokines followed by IL-12 and then IL-10, IL-1 alpha, I
L-1 beta, and IL-6, indicating a potential role for these events in ea
rly recruitment, activation, and interferon-gamma production of CD4 ce
lls in herpetic lesions.