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Suppression of macrophage activation with CNI-1493 increases survival in infant rats with systemic Haemophilus influenzae infection

Granert, Carl (author)
Division of Infectious Diseases, Department of Medicine, Karolinska Institute, Huddinge University Hospital, Stockholm, Sweden
Abdalla, Hana (author)
Division of Infectious Diseases, Department of Medicine, Karolinska Institute, Huddinge University Hospital, Stockholm, Sweden
Lindquist, Lars (author)
Karolinska Institutet
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Diab, Asim (author)
Division of Infectious Diseases, Department of Medicine, Karolinska Institute, Huddinge University Hospital, Stockholm, Sweden
Bahkiet, Moiz (author)
Division of Infectious Diseases, Department of Medicine, Karolinska Institute, Huddinge University Hospital, Stockholm, Sweden
Tracey, Kevin J. (author)
Laboratory of Biomedical Science, North Shore University Hospital, Manhasset, New York
Andersson, Jan (author)
Karolinska Institutet
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 (creator_code:org_t)
2000
2000
English.
In: Infection and Immunity. - 0019-9567 .- 1098-5522. ; 68:9, s. 5329-5334
  • Journal article (peer-reviewed)
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  • 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-α)-, interleukin 1 beta (IL-1β)-, and gamma interferon (IFN-γ)-producing cells in the spleen. A significant reduction of the incidence of TNF-α- and IL-1β-expressing cells was found for CNI-1493-treated animals. IFN-γ 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.

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