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Infection and Immunity, March 2000, p. 1243-1251, Vol. 68, No. 3
Division of Rheumatology, Toronto Western
Hospital,1 and Departments of
Medicine,2
Immunology,3 and Laboratory
Medicine and Pathobiology,4 University of
Toronto, Toronto, Canada
Received 2 August 1999/Returned for modification 30 September
1999/Accepted 12 November 1999
Tumor necrosis factor (TNF) has generally been regarded as a
protective cytokine in host defense against bacterial infections. In
the present study, we evaluated the role of TNF in the acute phase of
infection by Yersinia enterocolitica by using mice rendered genetically deficient in TNF receptor p55 (TNFRp55
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Copyright © 2000, American Society for Microbiology. All rights reserved.
Tumor Necrosis Factor Receptor p55-Deficient Mice
Respond to Acute Yersinia enterocolitica Infection with Less
Apoptosis and More Effective Host Resistance
/
).
Unexpectedly, TNFRp55
/
mice showed more effective
resistance to the bacteria, reflected in enhanced bacterial clearance
and less tissue damage, than did control C57BL/6 mice. C57BL/6 mice
showed evidence of extensive apoptosis in the spleen accompanied by a
selective decrease in the CD4+-T-cell population of
splenocytes, whereas TNFRp55
/
mice were spared these
changes. The splenocytes from TNFRp55
/
mice also
maintained a robust gamma interferon IFN-
response to mitogenic
stimulation, while the comparable response in C57BL/6 mice was
impaired. In addition, splenocytes harvested from infected mice
demonstrated lower production of interleukin-10 IL-10 in TNFRp55
/
mice than in C57BL/6 mice. These findings
suggest that Yersinia can induce TNFRp55-mediated apoptosis
of splenocytes in the acute phase of the infection and that
alteration of T-cell-generated cytokines can dramatically alter
the early events in host defense against this pathogen.
*
Corresponding author. Mailing address: The Toronto
Hospital Arthritis Center, The Toronto Hospital, 399 Bathurst St.,
Toronto, Ontario, M5T 2S8, Canada. Phone: (416) 603-5869. Fax: (416)
603-4348. E-mail: rinman{at}torhosp.toronto.on.ca.
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