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Covalent coupling of vitamin D3 to the major cat allergen Fel d 1 improves the effects of allergen-specific immunotherapy in a mouse model for cat allergy

机译:维生素D3与主要猫过敏原Fel d 1的共价偶联改善了对猫过敏的小鼠模型中过敏原特异性免疫疗法的作用

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Background: Allergen-specific immunotherapy (SIT) is currently the only curative treatment for allergy but the treatment needs to be improved. We hypothesize that covalent coupling of immunomodulating vitamin D3 to the major cat allergen Fel d 1 can enhance the beneficial effects of SIT to cat allergy. Methods: We treated mice sensitized to Fel d 1 with subcutaneous injections of two doses of recombinant Fel d 1 coupled to 1α,25-dihydroxyvitamin D3 (rFel d 1:VD3) and compared to treatment with the same doses of rFel d 1 in a mouse model for cat allergy. Airway hyperresponsiveness (AHR), cytokines and cells in bronchoalveolar lavage (BAL), in vitro activation of splenocytes to rFel d 1, and Fel d 1-specific immunoglobulins were evaluated. Results: Treatment with both doses of rFel d 1:VD3 decreased AHR, cellular influx and Th2 cytokines in BAL compared to untreated mice. High-and low-dose rFel d 1 treatment also decreased AHR and BAL Th2 cytokines, with less decrease for the low-dose treatment. Importantly, the total number of cells and eosinophils in BAL was markedly reduced at both high-and low-dose rFel d 1:VD3 compared to treatment with rFel d 1 alone. Finally, treatment with both rFel d 1 and rFel d 1:VD3 induced Fel d 1-specific serum IgG. Conclusion: Our results indicate a beneficial therapeutic effect of rFel d 1:VD3 on airway inflammation, AHR and rFel d 1-specific immune responses and thus suggest that this novel immunomodulatory candidate may improve both the efficacy and safety of SIT.
机译:背景:过敏原特异性免疫疗法(SIT)是目前唯一的过敏性治疗方法,但该治疗方法有待改进。我们假设免疫调节维生素D3与主要的猫过敏原Fel d 1共价偶联可以增强SIT对猫过敏的有益作用。方法:我们用皮下注射两种剂量的重组Fel d 1偶联1α,25-二羟基维生素D3(rFel d 1:VD3)来治疗对Fel d 1敏感的小鼠,并与在相同剂量的rFel d 1的治疗中进行比较。猫过敏的小鼠模型。评估气道高反应性(AHR),支气管肺泡灌洗(BAL)中的细胞因子和细胞,脾细胞在体外激活至rFel d 1和Fel d 1特异性免疫球蛋白的能力。结果:与未治疗的小鼠相比,两种剂量的rFel d 1:VD3均可降低BAL中的AHR,细胞内流和Th2细胞因子。高剂量和低剂量的rFel d 1治疗还减少了AHR和BAL Th2细胞因子,而低剂量治疗的减少较少。重要的是,与单独使用rFel d 1处理相比,高剂量和低剂量rFel d 1:VD3时BAL中的细胞和嗜酸性粒细胞总数均明显减少。最后,用rFel d 1和rFel d 1:VD3两者处理均可诱导Fel d 1特异性血清IgG。结论:我们的结果表明rFel d 1:VD3对气道炎症,AHR和rFel d 1特异性免疫反应具有有益的治疗作用,因此表明该新型免疫调节候选物可同时改善SIT的疗效和安全性。

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