House Dust Mite-Specific Sublingual Immunotherapy Prevents the Development of Allergic Inflammation in a Mouse Model of Experimental Asthma

被引:19
作者
Hagner, Stefanie [1 ]
Rask, Carola [3 ]
Brimnes, Jens [3 ]
Andersen, Peter Sejer [3 ]
Raifer, Hartmann [2 ]
Renz, Harald [1 ]
Garn, Holger [1 ]
机构
[1] Univ Marburg, Fac Med, Ctr Tumor & Immunobiol ZTI, Inst Lab Med, Hans Meerwein Str 3, DE-35043 Marburg, Germany
[2] Univ Marburg, Fac Med, Inst Med Microbiol & Hosp Hyg, Marburg, Germany
[3] ALK Abello, Dept Immunol, Horsholm, Denmark
关键词
Allergen immunotherapy; Dermatophagoides farinae; House dust mite; Sublingual; RANDOMIZED CONTROLLED-TRIAL; AIRWAY INFLAMMATION; DERMATOPHAGOIDES-FARINAE; NORTH-AMERICAN; DOUBLE-BLIND; TABLET ALK; FOLLOW-UP; EFFICACY; ADULTS; CHILDREN;
D O I
10.1159/000446155
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: Evidence regarding sublingual immunotherapy (SLIT) efficacy and its good safety profile has been demonstrated with pollen and house dust mite (HDM) allergens in the treatment of airway allergies. In addition, the use of grass pollen presents a SLIT disease-modifying treatment for respiratory allergies. Objectives: The aim of this study was to demonstrate the efficacy of HDM-based SLIT in mouse models of allergic airway inflammation and to gain insights into the involved local immunological mechanisms. Methods: Balb/c mice were sensitized/challenged with Dermatophagoides farinae (Der f) extract and underwent Der f-SLIT in prophylactic and therapeutic settings. The SLIT efficacy was assessed using lung function measurements, analysis of local inflammatory responses by bronchoalveolar lavage cell differentiation and lung histology. Humoral and cellular responses were monitored by ELISA, cytokine bead array and flow cytometry analyses. Results: In a prophylactic setting, Der f-SLIT with 12 development units per dose reduced the eosinophil-dominated inflammatory response in the lung paralleled by a marked reduction in airway hyperresponsiveness. Local Th2 responses were prevented as demonstrated by significantly lower levels of IL-5 and IL-13. Additionally, SLIT-treated mice revealed a lower proportion of CD4-CD8-gamma delta cells and a higher frequency of CD8+CD25+IFN gamma+T cells in the lungs compared to sham-treated mice. In a therapeutic setting, Der f-SLIT also resulted in reduced inflammatory responses in the lung. Conclusion: The efficacy of Der f-SLIT was demonstrated in prophylactic and therapeutic conditions using experimental mouse models of HDM-induced airway inflammation. A potential role of a so far underestimated lymphocyte subpopulation was also indicated. (C) 2016 S. Karger AG, Basel
引用
收藏
页码:22 / 34
页数:13
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