Abstract
BackgroundThe hygiene hypothesis suggests a link between parasitic infections and immune disorders, such as allergic diseases. We previously showed that infection with Toxoplasma gondii or systemic application of T. gondii tachyzoites lysate antigen (TLA) in a prophylactic, but not therapeutic protocol, prevented allergic airway inflammation in mice. Here we tested the effect of prophylactic and therapeutic application of TLA via the mucosal route.MethodsMice were intranasally treated with TLA either i) prior to sensitization, ii) during sensitization and challenge, or iii) after sensitization with ovalbumin (OVA). Recruitment of inflammatory cells to the lung, cytokine levels in restimulated lung and spleen cell cultures as well as levels of OVA-specific antibodies in serum were measured. In parallel, the effect of native TLA, heat-inactivated (hiTLA) or deglycosylated TLA (dgTLA) on sensitized splenocytes was evaluated ex vivo.ResultsWhen applied together with OVA i) during systemic sensitization and local challenge or ii) exclusively during local challenge, TLA reduced infiltration of eosinophils into the lung, OVA-specific type 2 cytokines in restimulated lung cell cultures, and partially, type 2 cytokines in restimulated spleen cell cultures in comparison to allergic controls. No beneficial effect was observed when TLA was applied prior to the start of sensitization. Analysis of epitope sugars on TLA indicated a high abundance of mannose, fucose, N-acetylglucosamine, and N-acetylgalactosamine. Deglycosylation of TLA, but not heat-inactivation, abolished the potential of TLA to reduce type 2 responses ex vivo, suggesting a significant role of carbohydrates in immunomodulation.ConclusionWe showed that mucosal application of TLA reduced the development of experimental allergy in mice. The beneficial effects depended on the timing of the application in relation to the time point of sensitization. Not only co-application, but also therapy in sensitized/allergic animals with native TLA reduced local allergic responses. Furthermore, we show that TLA is highly glycosylated and glycoconjugates seem to play a role in anti-allergic effects. In summary, given the powerful modulatory effect that TLA exhibits, understanding its exact mechanisms of action may lead to the development of novel immunomodulators in clinical application.
Highlights
Allergic diseases of the airways affect millions of people and the prevalence has been increasing continuously
Mice were sensitized by two i.p. injections of OVA in alum followed by three intranasal challenges of OVA one week later on days 21 to 23 (Figure 1A)
In a mouse model of allergy, we have previously demonstrated that infection with T. gondii or intraperitoneal application of tachyzoites lysate antigen (TLA) admixed to OVA in alum reduced type 2 responses accompanied by increased levels of allergen-specific IFN-g in restimulated splenocytes compared to allergic controls [22, 24]
Summary
Allergic diseases of the airways affect millions of people and the prevalence has been increasing continuously. Allergic asthma is a heterogeneous and complex inflammatory disease of the airways that develops upon allergic sensitization with allergens, such as house dust mites, cockroaches, animal dander, grass and tree pollens, and fungal spores [1]. These inhaled allergens stimulate the production of type 2 cytokines, such as IL-4, IL-5, and IL-13, leading to airway eosinophilia, airway hyperresponsiveness, mucus hypersecretion, and elevated IgE in serum [1, 2]. We tested the effect of prophylactic and therapeutic application of TLA via the mucosal route
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