Department of Immunology, Roswell Park Comprehensive Cancer Center, 665 Elm Street, Buffalo, NY, 14263, USA.
Department of Urology, Roswell Park Comprehensive Cancer Center, Buffalo, NY, USA.
Respir Res. 2023 Oct 31;24(1):261. doi: 10.1186/s12931-023-02568-2.
Due to the relatively short existence of alternative tobacco products, gaps exist in our current understanding of their long-term respiratory health effects. We therefore undertook the first-ever side-by-side comparison of the impact of chronic inhalation of aerosols emitted from electronic cigarettes (EC) and heated tobacco products (HTP), and combustible cigarettes (CC) smoke.
To evaluate the potential differential effects of alternative tobacco products on lung inflammatory responses and efficacy of vaccination in comparison to CC.
Mice were exposed to emissions from EC, HTP, CC, or air for 8 weeks. BAL and lung tissue were analyzed for markers of inflammation, lung damage, and oxidative stress. Another group was exposed for 12 weeks and vaccinated and challenged with a bacterial respiratory infection. Antibody titers in BAL and sera and pulmonary bacterial clearance were assessed.
EC- and HTP-aerosols significantly augmented lung immune cell infiltrates equivalent to that achieved following CC-exposure. HTP and CC significantly increased neutrophil numbers compared to EC. All products augmented numbers of B cells, T cells, and pro-inflammatory IL17A T cells in the lungs. Decreased lung antioxidant activity and lung epithelial and endothelial damage was induced by all products. EC and HTP differentially augmented inflammatory cytokines/chemokines in the BAL. Generation of immunity following vaccination was impaired by EC and HTP but to a lesser extent than CC, with a CC > HTP > EC hierarchy of suppression of pulmonary bacterial clearance.
HTP and EC-aerosols induced a proinflammatory pulmonary microenvironment, lung damage, and suppressed efficacy of vaccination.
由于替代烟草产品的存在时间相对较短,我们目前对其长期呼吸道健康影响的了解还存在空白。因此,我们首次对电子烟(EC)和加热烟草产品(HTP)气溶胶与可燃香烟(CC)烟雾的慢性吸入的影响进行了并列比较。
评估替代烟草产品对肺部炎症反应的潜在差异影响,并与 CC 进行比较,评估其对疫苗接种效果的影响。
将小鼠暴露于 EC、HTP、CC 或空气的排放物中 8 周。分析 BAL 和肺组织中的炎症、肺损伤和氧化应激标志物。另一组暴露 12 周,并进行疫苗接种和细菌呼吸道感染挑战。评估 BAL 和血清中的抗体滴度以及肺部细菌清除率。
EC 和 HTP 气溶胶显著增强了肺部免疫细胞浸润,与 CC 暴露相当。与 EC 相比,HTP 和 CC 显著增加了中性粒细胞数量。所有产品均增加了肺内 B 细胞、T 细胞和促炎 IL17A T 细胞的数量。所有产品均降低了肺抗氧化活性以及肺上皮和内皮损伤。EC 和 HTP 以不同的方式增强了 BAL 中的炎症细胞因子/趋化因子。疫苗接种后的免疫生成受到 EC 和 HTP 的损害,但比 CC 的损害程度要小,存在 CC > HTP > EC 的肺部细菌清除抑制层次结构。
HTP 和 EC 气溶胶诱导了促炎的肺部微环境、肺损伤,并抑制了疫苗接种的效果。