Academic Journal

Blocking antibodies induced by allergen‐specific immunotherapy ameliorate allergic airway disease in a human/mouse chimeric model

التفاصيل البيبلوغرافية
العنوان: Blocking antibodies induced by allergen‐specific immunotherapy ameliorate allergic airway disease in a human/mouse chimeric model
المؤلفون: Vizzardelli, C., Gindl, M., Roos, S., Möbs, C., Nagl, B., Zimmann, F., Sexl, V., Kenner, L., Neunkirchner, A., Zlabinger, G. J., Pickl, W. F., Pfützner, W., Bohle, B.
المساهمون: Austrian Science Fund
المصدر: Allergy ; volume 73, issue 4, page 851-861 ; ISSN 0105-4538 1398-9995
بيانات النشر: Wiley
سنة النشر: 2017
المجموعة: Wiley Online Library (Open Access Articles via Crossref)
الوصف: Background Allergen‐specific immunotherapy ( AIT ) induces specific blocking antibodies (Ab), which are claimed to prevent IgE‐mediated reactions to allergens. Additionally, AIT modulates cellular responses to allergens, for example, by desensitizing effector cells, inducing regulatory T and B lymphocytes and immune deviation. It is still enigmatic which of these mechanisms mediate(s) clinical tolerance. We sought to address the role of AIT ‐induced blocking Ab separately from cellular responses in a chimeric human/mouse model of respiratory allergy. Methods Nonobese diabetic severe combined immunodeficient γc −/− ( NSG ) mice received intraperitoneally allergen‐reactive PBMC from birch pollen‐allergic patients together with birch pollen extract and human IL ‐4. Engraftment was assessed by flow cytometry. Airway hyperresponsiveness ( AHR ) and bronchial inflammation were analyzed after intranasal challenges with allergen or PBS . Sera collected from patients before and during AIT with birch pollen were added to the allergen prior to intranasal challenge. The IgE‐blocking activity of post‐ AIT sera was assessed in vitro. Results Human cells were detected in cell suspensions of murine lungs and spleens indicating successful humanization. Humanized mice displayed a more pronounced AHR and bronchial inflammation when challenged with allergen compared to negative controls. Post‐ AIT sera exerted IgE‐blocking activity. In contrast to pre‐ AIT sera, the presence of heterologous and autologous post‐ AIT sera significantly reduced the allergic airway inflammation and matched their IgE‐blocking activity determined in vitro. Conclusion Our data demonstrate that post‐ AIT sera with IgE‐blocking activity ameliorate allergic airway inflammation in a human/mouse chimeric model of respiratory allergy independently of AIT ‐induced cellular changes.
نوع الوثيقة: article in journal/newspaper
اللغة: English
DOI: 10.1111/all.13363
الاتاحة: http://dx.doi.org/10.1111/all.13363
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fall.13363
https://onlinelibrary.wiley.com/doi/pdf/10.1111/all.13363
Rights: http://onlinelibrary.wiley.com/termsAndConditions#vor
رقم الانضمام: edsbas.6F445179
قاعدة البيانات: BASE