Cent Eur J Immunol. 2025;50(3):304-313. doi: 10.5114/ceji.2025.152018. Epub 2025 Oct 13.
ABSTRACT
INTRODUCTION: To explore the mechanism of action of azithromycin on lung oxidative injury and immune function in mice infected with Mycoplasma pneumoniae (MP) based on the nuclear factor E2-related factor 2/antioxidant response element (Nrf2/ARE) signaling pathway.
MATERIAL AND METHODS: The lung index, dry/wet weight ratio, inflammatory factor levels in alveolar lavage fluid, serum contents of interferon-ฮณ (IFN-ฮณ) and immunoglobulin G (IgG), oxidative stress markers, peripheral blood levels of T-lymphocyte subsets, pathological changes, and Nrf2, HO-1, and NQO1 expression were assessed.
RESULTS: Compared to the control group, the MP group exhibited elevated lung index, reduced lung dry/wet weight ratio, elevated tumor necrosis factor ฮฑ (TNF-ฮฑ), interleukin (IL)-1ฮฒ and IL-6 contents, reduced IL-10 levels, raised IFN-ฮณ, IgG and peripheral blood CD8+ levels, reduced CD3+ and CD4+ levels, CD4+/CD8+ ratio, and superoxide dismutase (SOD) and glutathione (GSH) activity, elevated malondialdehyde (MDA) contents, destruction of lung tissue structure, elevated pathological scores, and diminished Nrf2, HO-1, and NQO1 levels. Compared with MP and MP + DMSO groups, MP + azithromycin (AZI) and MP + sulforaphane (SFN) groups displayed a reduced lung index, elevated lung dry/wet weight ratio, reduced TNF-ฮฑ, IL-1ฮฒ, and IL-6 contents, raised IL-10 content, decreased IFN-ฮณ, IgG, and peripheral blood CD8+ levels, increased CD3+ and CD4+ levels and CD4+/CD8+ ratio, raised SOD and GSH activity, and diminished MDA content. HE staining demonstrated improved lung tissue structure, diminished pathological scores, and upregulated Nrf2, HO-1, and NQO1 levels after azithromycin and SFN intervention compared to the MP group (all p < 0.05).
CONCLUSIONS: Azithromycin ameliorates MP infection-induced lung injury and oxidative stress and strengthens immune function in mice, which may be achieved by activating the Nrf2/ARE signaling pathway.
PMID:41438358 | PMC:PMC12721244 | DOI:10.5114/ceji.2025.152018