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维生素 D3 与主要猫过敏原 Fel d 1 的共价偶联可改善变应原特异性免疫疗法在猫变应原小鼠模型中的效果。

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.

机构信息

Department of Medicine, Clinical Immunology and Allergy Unit, Karolinska Institutet, Stockholm, Sweden.

出版信息

Int Arch Allergy Immunol. 2012;157(2):136-46. doi: 10.1159/000327546. Epub 2011 Oct 5.

DOI:10.1159/000327546
PMID:21985799
Abstract

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.

摘要

背景

变应原特异性免疫治疗(SIT)是目前治疗过敏的唯一根治方法,但仍需改进。我们假设将免疫调节维生素 D3 共价偶联到主要的猫过敏原 Fel d 1 上,可以增强 SIT 对猫过敏的有益作用。

方法

我们用皮下注射两剂重组 Fel d 1 与 1α,25-二羟维生素 D3(rFel d 1:VD3)偶联的方法,对 Fel d 1 致敏的小鼠进行治疗,并与在猫过敏小鼠模型中用相同剂量 rFel d 1 治疗进行比较。评估气道高反应性(AHR)、支气管肺泡灌洗液(BAL)中的细胞因子和细胞、脾细胞对 rFel d 1 的体外激活,以及 Fel d 1 特异性免疫球蛋白。

结果

与未治疗的小鼠相比,两剂 rFel d 1:VD3 治疗均可降低 AHR、BAL 中的细胞浸润和 Th2 细胞因子。高剂量和低剂量 rFel d 1 治疗也可降低 AHR 和 BAL Th2 细胞因子,但低剂量治疗的降低幅度较小。重要的是,与单独用 rFel d 1 治疗相比,高剂量和低剂量 rFel d 1:VD3 治疗可显著减少 BAL 中的总细胞数和嗜酸性粒细胞数。最后,用 rFel d 1 和 rFel d 1:VD3 治疗均可诱导 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 特异性免疫反应有有益的治疗作用,因此表明这种新型免疫调节候选物可能会提高 SIT 的疗效和安全性。

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