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Stimulation of Macrophages by Endotoxin Results in the Reactivation of a Persistent Herpes Simplex Virus Infection
Author(s) -
DOMKEOPITZ I.,
KIRCHNER H
Publication year - 1990
Publication title -
scandinavian journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.934
H-Index - 88
eISSN - 1365-3083
pISSN - 0300-9475
DOI - 10.1111/j.1365-3083.1990.tb02895.x
Subject(s) - herpes simplex virus , lytic cycle , virus , lipopolysaccharide , macrophage , virology , tumor necrosis factor alpha , stimulation , biology , herpesviridae , cytopathic effect , immunology , microbiology and biotechnology , viral disease , in vitro , biochemistry , neuroscience
Previous work has shown that splenic macrophages derived from herpes simplex virus (HSV)‐resistant C57BL/6 mice undergo a persistent HSV infection which is characterized by the continuous release of infectious virus particles from a small subpopulation of infected cells. Treatment of persistently infected macrophages for 2 weeks with lipopolysaccharide (LPS) resulted in an increase of HSV yield and in virus‐induced cytopathic effects. HSV was also reactivated by treatment of macrophage cultures with lipid A or tumour necrosis factor (TNF). Like macrophages of C57 BL/6 origin, cells from LPS‐hyporesponsive C3H/HeJ mice could be persistently infected with HSV. These cells were resistant to LPS‐induced virus reactivation. The results show that macrophages derived from C57BL6 mice are rendered susceptible to lytic HSV infection by treatment with LPS or TNF. Thus, these substances may interfere with persistent HSV infection which can he established due to genetically controlled properties of the host.