Protective Effects of Anti-IL17 on Acute Lung Injury Induced by LPS in Mice

• Main Authors: Renato Fraga Righetti (Author), Tabata Maruyama dos Santos (Author), Leandro do Nascimento Camargo (Author), Luciana Ritha Cássia Rolim Barbosa Aristóteles (Author), Silvia Fukuzaki (Author), Flávia Castro Ribas de Souza (Author), Fernanda Paula Roncon Santana (Author), Marcus Vinicius Rodrigues de Agrela (Author), Maysa Mariana Cruz (Author), Maria Isabel Cardoso Alonso-Vale (Author), Isabella Santos Genaro (Author), Beatriz Mangueira Saraiva-Romanholo (Author), Edna Aparecida Leick (Author), Milton de Arruda Martins (Author), Carla Máximo Prado (Author), Iolanda de Fátima Lopes Calvo Tibério (Author)
• Format: Book
• Published: Frontiers Media S.A., 2018-10-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.
• Notes: 1663-9812; 10.3389/fphar.2018.01021
• Keywords: acute lung injury; inflammation mediators; interleukin 17; remodeling; oxidative stress; Therapeutics. Pharmacology; RM1-950
• Source: Frontiers in Pharmacology, Vol 9 (2018)

Introduction: T helper 17 (Th17) has been implicated in a variety of inflammatory lung and immune system diseases. However, little is known about the expression and biological role of IL-17 in acute lung injury (ALI). We investigated the mechanisms involved in the effect of anti-IL17 in a model of lipopolysaccharide (LPS)-induced acute lung injury (ALI) in mice.Methods: Mice were pre-treated with anti-IL17, 1h before saline/LPS intratracheal administration alongside non-treated controls and levels of exhaled nitric oxide (eNO), cytokine expression, extracellular matrix remodeling and oxidative stress, as well as immune cell counts in bronchoalveolar lavage fluid (BALF), and respiratory mechanics were assessed in lung tissue.Results: LPS instillation led to an increase in multiple cytokines, proteases, nuclear factor-κB, and Forkhead box P3 (FOXP3), eNO and regulators of the actomyosin cytoskeleton, the number of CD4+ and iNOS-positive cells as well as the number of neutrophils and macrophages in BALF, resistance and elastance of the respiratory system, ARG-1 gene expression, collagen fibers, and actin and 8-iso-PGF2α volume fractions. Pre-treatment with anti-IL17 led to a significant reduction in the level of all assessed factors.Conclusions: Anti-IL17 can protect the lungs from the inflammatory effects of LPS-induced ALI, primarily mediated by the reduced expression of cytokines and oxidative stress. This suggests that further studies using anti-IL17 in a treatment regime would be highly worthwhile.