Allergy · 2020 · 87 citations · 52 references
Life SciencesBotanyImmunologyAllergyHypersensitivityInflammationAllergic ConditionsAllergic DiseaseEnvironmental AllergensPollen AllergyPollen BiologyRespiratory AllergyAirborne Pollen ExposureAllergic Airway InflammationAllergic Disease MechanismsAllergic Disease ModelsClimate Change Effects On PollenClimate Effects On AllergiesPollen Allergen CharacterizationPollen Allergens
Abstract Background Common ragweed has been spreading as a neophyte in Europe. Elevated CO 2 levels, a hallmark of global climate change, have been shown to increase ragweed pollen production, but their effects on pollen allergenicity remain to be elucidated. Methods Ragweed was grown in climate‐controlled chambers under normal (380 ppm, control) or elevated (700 ppm, based on RCP4.5 scenario) CO 2 levels. Aqueous pollen extracts (RWE) from control‐ or CO 2 ‐pollen were administered in vivo in a mouse model for allergic disease (daily for 3‐11 days, n = 5) and employed in human in vitro systems of nasal epithelial cells (HNECs), monocyte‐derived dendritic cells (DCs), and HNEC‐DC co‐cultures. Additionally, adjuvant factors and metabolites in control‐ and CO 2 ‐RWE were investigated using ELISA and untargeted metabolomics. Results In vivo, CO 2 ‐RWE induced stronger allergic lung inflammation compared to control‐RWE, as indicated by lung inflammatory cell infiltrate and mediators, mucus hypersecretion, and serum total IgE. In vitro, HNECs stimulated with RWE increased indistinctively the production of pro‐inflammatory cytokines (IL‐8, IL‐1β, and IL‐6). In contrast, supernatants from CO 2 ‐RWE‐stimulated HNECs, compared to control‐RWE‐stimulated HNECS, significantly increased TNF and decreased IL‐10 production in DCs. Comparable results were obtained by stimulating DCs directly with RWEs. The metabolome analysis revealed differential expression of secondary plant metabolites in control‐ vs CO 2 ‐RWE. Mixes of these metabolites elicited similar responses in DCs as compared to respective RWEs. Conclusion Our results indicate that elevated ambient CO 2 levels elicit a stronger RWE‐induced allergic response in vivo and in vitro and that RWE increased allergenicity depends on the interplay of multiple metabolites.
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