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Infection and Immunity, April 1999, p. 1789-1797, Vol. 67, No. 4
0019-9567/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Rapid Local Expression of Interleukin-12, Tumor
Necrosis Factor Alpha, and Gamma Interferon after Cutaneous
Francisella tularensis Infection in Tularemia-Immune
Mice
Stephan
Stenmark,1
Dan
Sunnemark,2
Anders
Bucht,3,4 and
Anders
Sjöstedt1,5,*
Department of Infectious Diseases, University
of Umeå,1 and Department of
Biomedicine4 and Department of
Microbiology,5 Defence Research Establishment,
Umeå, and Microbiology and Tumorbiology
Centre2 and Department of
Rheumatology,3 Karolinska Institute,
Stockholm, Sweden
Received 18 August 1998/Returned for modification 8 October
1998/Accepted 5 January 1999
Francisella tularensis LVS is an effective live vaccine
strain used for cutaneous vaccination against tularemia in man. In mice, injection of LVS causes invasive disease and subsequent development of immunity that is characterized by effective control of
otherwise lethal doses of the organism. In the present investigation, it is shown that LVS-immune mice controlled an intradermal infection much more effectively than did naive mice; bacterial counts in skin
samples were 1.5 to 2.0 log10 lower 24 h after
injection and 6 log10 lower 72 h after injection in
immune mice. Moreover, in contrast to naive mice, no bacteria were
demonstrated in samples from livers and spleens of immune mice. By
immunohistochemistry, skin samples from immune mice showed an intense
staining for interleukin-12 (IL-12) and a moderate staining for tumor
necrosis factor alpha (TNF-
) at 24 h postinoculation, after
which staining for both cytokines faded. In naive mice, the staining
for IL-12 was weak at all time points and no staining for TNF-
was
observed. No staining for gamma interferon (IFN-
) was observed in
any group before 72 h. At that time point, skin samples from
immune mice showed moderate staining and skin samples from naive mice
showed weak staining. Reverse transcriptase PCR showed an induction of mRNA of the three cytokines in the skin within the first day after injection. A quantitative analysis demonstrated higher IFN-
and TNF-
mRNA levels in immune mice at 24 h postinoculation. In
conclusion, immunization with F. tularensis LVS conferred a
capability to respond to cutaneous reinfection, with rapid local
expression of IL-12, TNF-
, and IFN-
, and this expression was
paralleled by containment and mitigation of the infection. The cytokine
response may be part of a local barrier function of the skin, important to host protection against tularemia.
*
Corresponding author. Mailing address: Department of
Microbiology, Defence Research Establishment, S-901 82 Umeå, Sweden. Phone: 46-90-106665. Fax: 46-90-106806. E-mail:
sjostedt{at}ume.foa.se.
Infection and Immunity, April 1999, p. 1789-1797, Vol. 67, No. 4
0019-9567/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
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