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

Citation
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
Citations number
48
Categorie Soggetti
Infectious Diseases
ISSN journal
00221899
Volume
177
Issue
4
Year of publication
1998
Pages
827 - 838
Database
ISI
SICI code
0022-1899(1998)177:4<827:IPOCAB>2.0.ZU;2-Y
Abstract
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.