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Infection and Immunity, September 2000, p. 5329-5334, Vol. 68, No. 9
Division of Infectious Diseases, Department of Medicine,
Karolinska Institute, Huddinge University Hospital, Stockholm,
Sweden,1 and Laboratory of Biomedical
Science, North Shore University Hospital, Manhasset, New
York2
Received 16 February 2000/Returned for modification 3 April
2000/Accepted 16 June 2000
CNI-1493, a potent macrophage deactivator, was used to treat infant
rats systemically infected with Haemophilus influenzae type
b (Hib). CNI-1493 was injected 1 h prior to bacterial inoculation and 24 h later and resulted in a 75 percent increased rate of survival compared to that for untreated controls. The effect of CNI-1493 on the inflammatory response was studied by
immunohistochemical detection of individual tumor necrosis factor alpha
(TNF-
0019-9567/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Suppression of Macrophage Activation with CNI-1493 Increases
Survival in Infant Rats with Systemic Haemophilus
influenzae Infection
)-, interleukin 1 beta (IL-1
)-, and gamma interferon
(IFN-
)-producing cells in the spleen. A significant reduction of the
incidence of TNF-
- and IL-1
-expressing cells was found for
CNI-1493-treated animals. IFN-
expression was not suppressed by
CNI-1493, indicating that cytokine inhibition was specific in
macrophages. CNI-1493 significantly reduced the number of infiltrating
granulocytes in the brain from that for controls. This study provides
evidence that CNI-1493 protects against lethal Hib infection by
deactivating the inflammatory cascade in infant rats.
*
Corresponding author. Mailing address: Dept. of
Infectious Diseases I-73, Huddinge University Hospital, S-141 86 Huddinge, Sweden. Phone: 46-8-585 81953. Fax: 46-8-585 81916. E-mail:
carl.granert{at}medhs.ki.se.
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