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Regulation by interferons of the local inflammatory response to bacterial lipopolysaccharide
Abstract:
Footpad swelling developing in mice after local injection of LPS (S. marcescens) was found to consist of two phases with peaks occurring on days 2 to 3 and 6 to 8, respectively. Histopathologically, the reaction was characterized by edema and mononuclear cell infiltration; the second peak was associated with intravascular thrombosis as is typically described for the Shwartzman reaction to LPS. Recombinant DNA-derived IFN-gamma, administered by i.p. injection, had a suppressive effect on the development of the reaction. The same effect was seen with recombinant DNA-derived IFN-alpha 1 and with the natural mixture of IFN-alpha and -beta. In mice pretreated with neutralizing monoclonal antibodies to IFN-gamma, the footpad response to LPS was modified in that a delayed monophasic rather than a biphasic response occurred. These data indicate that LPS induces local production of IFN-gamma, which acts as a trigger or positive regulator of the reaction. The effect of a single pretreatment with neutralizing anti-IFN-gamma antibody was found to last for as long as 6 wk. Experiments in which antibody administration was delayed till after LPS challenge indicated that endogenous IFN-gamma was also involved in the late phases of the inflammation. The results show that regulation of inflammation by interferons is complex in that local IFN-gamma acts as a positive factor, whereas systemic IFN-alpha 1 and -gamma, probably through indirect mechanisms, downregulate inflammation.
Insights
Lipopolysaccharide (LPS) triggers a biphasic inflammatory response in mice, regulated by interferons (IFNs). Local IFN-gamma promotes inflammation, while systemic IFNs suppress it, revealing a complex regulatory role in immune responses.
Area of Science:
- Immunology
- Inflammation Research
Background:
- Lipopolysaccharide (LPS) from *S. marcescens* induces a biphasic inflammatory footpad swelling in mice.
- This reaction, resembling the Shwartzman reaction, involves edema, mononuclear cell infiltration, and intravascular thrombosis.
Purpose of the Study:
- To investigate the role of interferons (IFNs) in regulating LPS-induced inflammation.
- To elucidate the distinct roles of local versus systemic IFN production in modulating the inflammatory response.
Main Methods:
- Induction of footpad swelling in mice using LPS injection.
- Administration of recombinant interferons (IFN-gamma, IFN-alpha 1, IFN-alpha/beta) and neutralizing monoclonal antibodies against IFN-gamma.
- Histopathological analysis and assessment of inflammatory phases.
Main Results:
- Recombinant IFN-gamma, IFN-alpha 1, and IFN-alpha/beta suppressed the LPS-induced swelling.
- Neutralizing anti-IFN-gamma antibodies altered the biphasic response to a delayed monophasic reaction.
- Endogenous IFN-gamma was involved in both early and late phases of inflammation, with antibody effects lasting up to 6 weeks.
Conclusions:
- Local IFN-gamma acts as a positive regulator or trigger for LPS-induced inflammation.
- Systemic administration of IFN-alpha 1 and IFN-gamma can downregulate inflammation, likely via indirect mechanisms.
- Interferon regulation of inflammation is complex, with context-dependent pro- and anti-inflammatory roles.