Abstract
The benefits of moderate aerobic physical exercise for allergic asthma are well-known, particularly that of the anti-inflammatory effect that occurs by reducing Th2 responses and lung remodeling. However, the mechanisms of this immunoregulation are still under investigation. In this study, we investigated the possible immunoregulatory mechanisms of lung inflammation induced by moderate aerobic exercise in an experimental asthma model. BALB/c mice were distributed into Control, Exercise (EX), OVA, and OEX groups. OVA and OEX groups were sensitized with ovalbumin (OVA) on days 0, 14, 21, 28, and 42 and were challenged with OVA aerosol three times a week from days 21 to 51. The EX and OEX groups underwent moderate aerobic physical exercise from days 21 to 51 (5 d/w, 1 h/d). The mice were euthanized on day 52. We evaluated pulmonary cytokine production, serum immunoglobulin levels, and the inflammatory cell profile in lung and mediastinal lymph nodes. OVA mice showed increased expression of IL-4, IL-6, IL-10, and TGF-β and decreased macrophage type 2 (M2) recruitment. Physical exercise did not affect the increased antibody production of IgG2a, IgG1, or IgE induced by OVA. Of note, physical exercise alone markedly increased production of anti-inflammatory cytokines such as IL-10 and TGF-β. Physical exercise in OVA-mice also increased the recruitment of M2 in the lungs, as well as the influx and activation of regulatory T cells (Tregs) and CD4 and CD8 lymphocytes. In the draining lymph nodes, it was also observed that physical exercise increased the activation of CD4 T cells, regardless of the presence of OVA. Notably, physical exercise decreased common dendritic cells' (cDCs; pro-inflammatory) expression of co-stimulatory molecules such as CD80, CD86, and ICOSL in the draining lymph nodes, as well as increased ICOSL in plasmacytoid dendritic cells (pDCs; anti-inflammatory). Together, these findings show that physical exercise modulates pulmonary allergic inflammation by increasing Treg and M2 recruitment, as well as pDCs activation, which leads to an increase in anti-inflammatory cytokines and a decrease in pro-inflammatory cells and mediators.
Highlights
Asthma is a heterogeneous disease characterized by the chronic inflammation of the airways and variable remodeling [1]
The results showed an increase of IgG1 and IgG2a levels in ovalbumin-sensitized groups compared to non-sensitized animals
The OVA-specific immunoglobulin dosage in the serum of the OVA group demonstrated a significant increase in IgG1, IgG2a, and IgE levels, which were not altered by physical exercise
Summary
Asthma is a heterogeneous disease characterized by the chronic inflammation of the airways and variable remodeling [1]. Aerobic exercise has been used in several rehabilitation programs for asthmatic patients, resulting in decreased dyspnea, airway hyperresponsiveness, the induction of bronchospasm and even corticosteroid use. These patients demonstrate improvements in aerobic capacity and quality of life [3, 4]. Mackenzie et al [7] have shown that animals sensitized to ovalbumin (OVA) and submitted to an experimental exercise protocol demonstrate reduced IL-4, IL-5, and IL-13 levels in the mediastinal lymph nodes. This same study demonstrated that physical exercise inhibits maturation and the activation of dendritic cells, indicating that the decrease in Th2 response in sensitized and trained animals may be due to some interference in the maturation of the OVA antigen presenting cell during the exercise [7]
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