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Infection and Immunity, December 1998, p. 5862-5866, Vol. 66, No. 12
Department of Microbiology and Immunology,
Temple University School of Medicine, Philadelphia, Pennsylvania
19140
Received 20 July 1998/Returned for modification 1 September
1998/Accepted 21 September 1998
Splenocytes isolated from C57BL/6J female mice 3 to 7 days after
inoculation with an attenuated strain of Salmonella
typhimurium produced high levels of nitric oxide (39 to 77 µM)
and gamma interferon (IFN-
0019-9567/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Salmonella typhimurium Infection in Mice Induces
Nitric Oxide-Mediated Immunosuppression through a Natural
Killer Cell-Dependent Pathway

). Additionally, spleen cell cultures from
Salmonella-inoculated mice were markedly suppressed in
their ability to generate an in vitro plaque-forming cell (PFC)
response to sheep erythrocytes. Depletion of natural killer (NK) cells
from the immune splenocyte population markedly reduced nitric oxide
production, prevented suppression of PFC responses, and completely
abrogated IFN-
release. Treatment of NK cell-depleted immune cells
with IFN-
restored nitric oxide production to levels comparable to
those of intact immune cells and also restored the immunosuppression.
These results suggest that NK cells regulate the induction of nitric
oxide-mediated immunosuppression following infection with S. typhimurium through the production of IFN-
.
*
Corresponding author. Mailing address: Department of
Microbiology and Immunology, Temple University School of Medicine, 3400 North Broad St., Philadelphia, PA 19140. Phone: (215) 707-3585. Fax:
(215) 707-7920. E-mail: tke{at}astro.ocis.temple.edu.
Present address: Center for Surgical Research, Department of
Surgery, Brown University School of Medicine and Rhode Island Hospital,
Providence, RI 02903.
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