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Journal of Virology, March 1999, p. 1767-1773, Vol. 73, No. 3
Departments of
Ophthalmology1 and
Pathology and
Microbiology,2 University of Bristol, Bristol
BS8 1TD, United Kingdom
Received 21 September 1998/Accepted 12 November 1998
Reactivation of herpes simplex virus type 1 (HSV-1) in the
trigeminal ganglion (TG) was induced by UV irradiation of the corneas of latently infected mice. Immunocytochemistry was used to monitor the
dynamics of cytokine (interleukin-2 [IL-2], IL-4, IL-6, IL-10, gamma
interferon [IFN-
0022-538X/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Reactivation of Herpes Simplex Virus Type 1 in the
Mouse Trigeminal Ganglion: an In Vivo Study of Virus Antigen
and Cytokines
], and tumor necrosis factor alpha [TNF-
]) and viral antigen production in the TG and the adjacent central nervous
system on days 1 to 4, 6, 7, and 10 after irradiation. UV irradiation
induced increased expression of IL-6 and TNF-
from satellite cells
in uninfected TG. In latently infected TG, prior to reactivation, all
satellite cells were TNF-
+ and most were also
IL-6+. Reactivation, evidenced by HSV-1 antigens and/or
infiltrating immune cells, occurred in 28 of 45 (62%) TG samples.
Viral antigens were present in the TG in neurons, often disintegrating
on days 2 to 6 after irradiation. Infected neurons were usually
surrounded by satellite cells and the foci of immune cells producing
TNF-
and/or IL-6. IL-4+ cells were detected as early as
day 3 and were more numerous by day 10 (a very few IL-2+
and/or IFN-
+ cells were seen at this time). No IL-10 was
detected at any time. Our observations indicate that UV irradiation of
the cornea may modulate cytokine production by satellite cells. We
confirm that neurons are the site of reactivation and that they
probably do not survive this event. The predominance of TNF-
and
IL-6 following reactivation parallels primary infection in the TG and
suggests a role in viral clearance. The presence of Th2-type cytokines (IL-4 and IL-6) indicates a role for antibody. Thus, several clearance mechanisms may be at work.
*
Corresponding author. Mailing address: Department of
Ophthalmology, School of Medical Sciences, University Walk, Bristol BS8 1TD, United Kingdom. Phone: 44-117-9287627. Fax: 44-117-9287896. E-mail: C.Shimeld{at}bris.ac.uk.
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