Journal of Virology, August 1999, p. 6380-6386, Vol. 73, No. 8
0022-538X/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Division of Infectious Diseases, Children's Hospital Medical Center, and Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio 45229
Received 24 February 1999/Accepted 3 May 1999
Large numbers of polymorphonuclear leukocytes (PMNs) infiltrated
the murine vaginal mucosa within 24 h after intravaginal inoculation with an attenuated strain of herpes simplex virus type 2 (HSV-2). The role of these cells in resolution of a primary genital
infection and in protection of HSV-immune animals against challenge
with a fully virulent HSV-2 strain was investigated. Depletion of
greater than 95% of the PMNs at the vaginal mucosal surface prior to
intravaginal inoculation with an attenuated HSV-2 strain resulted in
significantly higher virus titers on days 3 to 7 but only slightly
delayed resolution of the primary genital infection. These results
suggest that neutrophils helped control the infection but that other
immune mechanisms ultimately cleared the virus. Interestingly,
depletion of PMNs from HSV-immune mice prior to challenge with a fully
virulent HSV-2 strain resulted in a rise in virus titers to levels
comparable to those of nonimmune mice and a more pronounced diminution
of virus clearance from the vaginal mucosa despite the presence of
HSV-specific B and T cells. Levels of gamma interferon (IFN-
) and
HSV-specific antibody were comparable in neutrophil-depleted and
control-treated immune mice following HSV-2 challenge, suggesting that
RB6-8C5 treatment did not impair T- and B-cell function. Therefore,
these results suggest that neutrophils play a role in limiting and
clearing HSV-2 vaginal infections and that they are, in association
with HSV-specific B and T cells, an important component in immune
protection of the vaginal mucosa.
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