Preventive and therapeutic effect of anti-IL-17 in an experimental model of elastase-induced lung injury in C57Bl6 mice

Author:

Fukuzaki Silvia1ORCID,Righetti Renato Fraga12,Santos Tabata Maruyama dos12,Camargo Leandro do Nascimento12,Aristóteles Luciana R. C. R. B.1,Souza Flavia C. R1,Garrido Aurelio C.1,Saraiva-Romanholo Beatriz Mangueira13,Leick Edna Aparecida1,Prado Carla Máximo14,Martins Mílton de Arruda1,Tibério Iolanda de Fátima Lopes Calvo1

Affiliation:

1. School of Medicine-Faculty of Medicine, University of São Paulo, São Paulo, São Paulo, Brazil

2. Hospital Sírio-Libanês, São Paulo, Brazil

3. Department of Medicine (LIM 20), Hospital Public Employee of São Paulo (Instituto de Assistência Médica ao Servidor Público Estadual de São Paulo), University City of São Paulo, São Paulo, Brazil

4. Department of Bioscience, Federal University of São Paulo, Santos, São Paulo, Brazil

Abstract

Chronic obstructive pulmonary disease (COPD) is an important health care issue, and IL-17 can modulate inflammatory responses. We evaluated preventive and therapeutic effect of anti-interleukin (IL)-17 in a model of lung injury induced by elastase, using 32 male C57Bl6 mice, divided into 4 groups: SAL, ELASTASE CONTROL (EC), ELASTASE + PREVENTIVE ANTI-IL-17 (EP), and ELASTASE + THERAPEUTIC ANTI-IL-17 (ET). On the 29th day, animals were anesthetized with thiopental, tracheotomized, and placed on a ventilator to evaluate lung mechanical, exhaled nitric oxide (eNO), and total cells of bronchoalveolar lavage fluid was collected. We performed histological techniques, and linear mean intercept (Lm) was analyzed. Both treatments with anti-IL-17 decreased respiratory resistance and elastance, airway resistance, elastance of pulmonary parenchyma, eNO, and Lm compared with EC. There was reduction in total cells and macrophages in ET compared with EC. Both treatments decreased nuclear factor-кB, inducible nitric oxide synthase, matrix metalloproteinase (MMP)-9, MMP-12, transforming growth factor-β, tumor necrosis factor-α, neutrophils, IL-1β, isoprostane, and IL-17 in airways and alveolar septa; collagen fibers, decorin and lumican in airways; and elastic fibers and fibronectin in alveolar septa compared with EC. There was reduction of collagen fibers in alveolar septa and biglycan in airways in EP and a reduction of eNO synthase in airways in ET. In conclusion, both treatments with anti-IL-17 contributed to improve most of parameters evaluated in inflammation and extracellular matrix remodeling in this model of lung injury.

Funder

Fundação de Amparo à Pesquisa do Estado de São Paulo

Conselho Nacional de Desenvolvimento Científico and Tecnológico

Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo

Publisher

American Physiological Society

Subject

Cell Biology,Physiology

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