Blockade of macrophage migration inhibitory factor (MIF) prevents the antigen-induced response in a murine model of allergic airway inflammation
T Amano, J Nishihira, I Miki - Inflammation Research, 2007 - Springer
T Amano, J Nishihira, I Miki
Inflammation Research, 2007•SpringerObjective and Design: The role of macrophage migration inhibitory factor (MIF), a
proinflammatory cytokine, was tested using a mouse asthma model. Materials: One hundred
and four male BALB/c mice were used in this study. Treatment: Mice were actively sensitized
with an intraperitoneal injection of ovalbumin (OVA) and challenged with repeated
nebulization of 1 w/v% OVA. Polyclonal anti-MIF antibody was intraperitoneally injected at
10 mg/kg during the antigen challenge period. Methods: Bronchoalveolar lavage (BAL) was …
proinflammatory cytokine, was tested using a mouse asthma model. Materials: One hundred
and four male BALB/c mice were used in this study. Treatment: Mice were actively sensitized
with an intraperitoneal injection of ovalbumin (OVA) and challenged with repeated
nebulization of 1 w/v% OVA. Polyclonal anti-MIF antibody was intraperitoneally injected at
10 mg/kg during the antigen challenge period. Methods: Bronchoalveolar lavage (BAL) was …
Objective and Design
The role of macrophage migration inhibitory factor (MIF), a proinflammatory cytokine, was tested using a mouse asthma model.
Materials
One hundred and four male BALB/c mice were used in this study.
Treatment
Mice were actively sensitized with an intraperitoneal injection of ovalbumin (OVA) and challenged with repeated nebulization of 1 w/v% OVA. Polyclonal anti-MIF antibody was intraperitoneally injected at 10 mg/kg during the antigen challenge period.
Methods
Bronchoalveolar lavage (BAL) was performed 8 h after the last challenge. Airway hyperresponsiveness to inhaled methacholine was measured 24 h after the last challenge.
Results
Antigen challenge to immunized mice induced increase in inflammatory cells and concentration of Th2 cytokines in BAL fluid (BALF), and caused the development of airway hyperresponsiveness. Anti-MIF antibody significantly decreased the numbers of inflammatory cells including macrophages, eosinophils, lymphocytes and neutrophils in BALF from OVA-challenged mice. Prednisolone decreased the numbers of eosinophils, lymphocytes and neutrophils but not macrophages. Anti-MIF antibody reduced airway hyperresponsiveness. Anti-MIF antibody affected neither the cytokine levels in BALF nor the IgE levels in serum.
Conclusion
MIF was involved in the antigen-induced inflammatory cell accumulation in the lung and airway hyperresponsiveness without affecting immune responses.
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