Role of histamine in natural killer cell-dependent protection against herpes simplex virus type 2 infection in mice

Author:

Hellstrand K1,Asea A1,Hermodsson S1

Affiliation:

1. Department of Clinical Virology, University of Göteborg, Sweden.

Abstract

Depletion of natural killer (NK) cells in vivo with anti-NK1.1 monoclonal antibody or anti-asialo-GM1 antiserum drastically reduced survival time in Swiss albino mice infected intravenously (i.v.) with herpes simplex virus type 2 (HSV-2). In contrast, depletion of NK cells did not affect the survival time of mice inoculated with HSV-2 by the intraperitoneal route. A single dose of histamine prolonged survival time in animals inoculated with HSV-2 i.v. but not in animals infected intraperitoneally. Treatment with the histamine H2 receptor antagonist ranitidine alone reduced survival time in i.v.-infected animals and blocked the protective effect of histamine. Histamine or ranitidine did not affect survival time in anti-NK1.1- or anti-asialo-GM1-treated animals. Our data suggest a role for histaminergic mechanisms in NK cell-mediated protection against HSV-2.

Publisher

American Society for Microbiology

Subject

Microbiology (medical),Clinical Biochemistry,Immunology,Immunology and Allergy

Reference34 articles.

1. Induction of natural killer cells by herpes simplex virus type 2 in resistant and sensitive inbred mouse strains;Ammerding D.;Immunobiology,1981

2. .Asea A. et al. Submitted for publication.

3. Bergström T. 1991. Neuropathogenicity of herpes simplex virus p. 7-47. Ph.D. thesis. University of Göteborg Göteborg Sweden.

4. Activation of human natural killer cells by herpes simplex virus type 1-infected cells;Bishop G. A.;Intervirology,1987

5. Adoptive transfer studies demonstrating the antiviral effects of NK cells in vivo;Bukowski J. F.;J. Exp. Med.,1985

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