IκB kinase β inhibitor, IMD-0354, prevents allergic asthma in a mouse model through inhibition of CD4+ effector T cell responses in the lung-draining mediastinal lymph nodes
Autor: | Agnieszka Jasiecka, Jerzy Jan Jaroszewski, Iwona Otrocka-Domagała, Tomasz Maślanka, Monika Zuśka-Prot, M. Mikiewicz, Jagoda Przybysz |
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Rok vydání: | 2016 |
Předmět: |
CD4-Positive T-Lymphocytes
0301 basic medicine Ovalbumin T cell Inflammation IκB kinase Allergic inflammation 03 medical and health sciences 0302 clinical medicine medicine Animals Anti-Asthmatic Agents IL-2 receptor Lung Pharmacology Mice Inbred BALB C biology FOXP3 Allergens respiratory system Asthma I-kappa B Kinase Disease Models Animal 030104 developmental biology medicine.anatomical_structure Benzamides Immunology biology.protein Lymph Nodes Lymph medicine.symptom 030215 immunology |
Zdroj: | European Journal of Pharmacology. 775:78-85 |
ISSN: | 0014-2999 |
DOI: | 10.1016/j.ejphar.2016.02.023 |
Popis: | IκB kinase (IKK) is important for nuclear factor (NF)-κB activation under inflammatory conditions. It has been demonstrated that IMD-0354, i.e. a selective inhibitor of IKKβ, inhibited allergic inflammation in a mouse model of ovalbumin (OVA)-induced asthma. The present study attempts to shed light on the involvement of CD4(+) effector (Teff) and regulatory (Treg) T cells in the anti-asthmatic action of IMD-0354. The animals were divided into three groups: vehicle treated, PBS-sensitized/challenged mice (PBS group); vehicle treated, OVA-sensitized/challenged mice (OVA group); and IMD-0354-treated, OVA-sensitized/challenged mice. The analyzed parameters included the absolute counts of Treg cells (Foxp3(+)CD25(+)CD4(+)), activated Teff cells (Foxp3(-)CD25(+)CD4(+)) and resting T cells (CD25(-)CD4(+)) in the mediastinal lymph nodes (MLNs), lungs and peripheral blood. Moreover, lung histopathology was performed to evaluate lung inflammation. It was found that the absolute number of cells in all studied subsets was considerably increased in the MLNs and lungs of mice from OVA group as compared to PBS group. All of these effects were fully prevented by treatment with IMD-0354. Histopathological examination showed that treatment with IMD-0354 protected the lungs from OVA-induced allergic airway inflammation. Our results indicate that IMD-0354 exerts anti-asthmatic action, at least partially, by blocking the activation and clonal expansion of CD4(+) Teff cells in the MLNs, which, consequently, prevents infiltration of the lungs with activated CD4(+) Teff cells. The beneficial effects of IMD-0354 in a mouse model of asthma are not mediated through increased recruitment of Treg cells into the MLNs and lungs and/or local generation of inducible Treg cells. |
Databáze: | OpenAIRE |
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