Enhanced efficacy of sublingual immunotherapy by liposome-mediated delivery of allergen
Have Aliu,1–3 Carola Rask,1 Jens Brimnes,1 Thomas Lars Andresen2,3 1Immunology Department, In vivo Biology Team, ALK Abelló A/S, Hørsholm, 2Department of Micro- and Nanotechnology, Technical University of Denmark, 3Center for Nanomedicine and Theranostics, Technical...
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Dove Medical Press
2017
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oai:doaj.org-article:8b809d56112c4111a4e1ab7c25129a1f2021-12-02T00:07:18ZEnhanced efficacy of sublingual immunotherapy by liposome-mediated delivery of allergen1178-2013https://doaj.org/article/8b809d56112c4111a4e1ab7c25129a1f2017-11-01T00:00:00Zhttps://www.dovepress.com/enhanced-efficacy-of-sublingual-immunotherapy-by-liposome-mediated-del-peer-reviewed-article-IJNhttps://doaj.org/toc/1178-2013Have Aliu,1–3 Carola Rask,1 Jens Brimnes,1 Thomas Lars Andresen2,3 1Immunology Department, In vivo Biology Team, ALK Abelló A/S, Hørsholm, 2Department of Micro- and Nanotechnology, Technical University of Denmark, 3Center for Nanomedicine and Theranostics, Technical University of Denmark, Kgs Lyngby, Denmark Abstract: Immunotherapy by sublingual administration of allergens provides high patient compliance and has emerged as an alternative to subcutaneous immunotherapy for the ­treatment of IgE-associated allergic diseases. However, sublingual immunotherapy (SLIT) can cause adverse events. Development of allergen delivery systems enabling more efficient delivery and hence lower allergen load might reduce the adverse events. In the present study, we have investigated neutral and cationic liposomes as delivery systems of ovalbumin (OVA), as a model allergen, in an OVA-induced allergic airway inflammation model. We investigated the liposome carriers’ ability to improve tolerance induction of antigens compared to the ­corresponding dose of free OVA. Mice were treated sublingually over 2 weeks with free or liposome encapsulated OVA followed by intraperitoneal injections and intranasal challenge. Mice sublingually treated with OVA-liposomes showed a significant reduction of airway eosinophilia and splenocyte proliferation in comparison to free OVA. A similar nonsignificant pattern was seen for OVA-specific IgE antibodies. In addition, reduced levels of interferon-γ and interleukin-5 were observed in spleen cell culture supernatants from OVA-liposome-treated mice compared to the sham-treated group. In conclusion, in vivo efficacy data showed that prophylactic SLIT with OVA-liposomes is significantly more effective in preventing allergic inflammation than the corresponding dose of free OVA. Keywords: sublingual immunotherapy, drug delivery, allergy, liposome Aliu HRask CBrimnes JAndresen TLDove Medical PressarticleSublingual ImmunotherapyDrug DeliveryAllergyMedicine (General)R5-920ENInternational Journal of Nanomedicine, Vol Volume 12, Pp 8377-8388 (2017) |
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Sublingual Immunotherapy Drug Delivery Allergy Medicine (General) R5-920 |
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Sublingual Immunotherapy Drug Delivery Allergy Medicine (General) R5-920 Aliu H Rask C Brimnes J Andresen TL Enhanced efficacy of sublingual immunotherapy by liposome-mediated delivery of allergen |
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Have Aliu,1–3 Carola Rask,1 Jens Brimnes,1 Thomas Lars Andresen2,3 1Immunology Department, In vivo Biology Team, ALK Abelló A/S, Hørsholm, 2Department of Micro- and Nanotechnology, Technical University of Denmark, 3Center for Nanomedicine and Theranostics, Technical University of Denmark, Kgs Lyngby, Denmark Abstract: Immunotherapy by sublingual administration of allergens provides high patient compliance and has emerged as an alternative to subcutaneous immunotherapy for the ­treatment of IgE-associated allergic diseases. However, sublingual immunotherapy (SLIT) can cause adverse events. Development of allergen delivery systems enabling more efficient delivery and hence lower allergen load might reduce the adverse events. In the present study, we have investigated neutral and cationic liposomes as delivery systems of ovalbumin (OVA), as a model allergen, in an OVA-induced allergic airway inflammation model. We investigated the liposome carriers’ ability to improve tolerance induction of antigens compared to the ­corresponding dose of free OVA. Mice were treated sublingually over 2 weeks with free or liposome encapsulated OVA followed by intraperitoneal injections and intranasal challenge. Mice sublingually treated with OVA-liposomes showed a significant reduction of airway eosinophilia and splenocyte proliferation in comparison to free OVA. A similar nonsignificant pattern was seen for OVA-specific IgE antibodies. In addition, reduced levels of interferon-γ and interleukin-5 were observed in spleen cell culture supernatants from OVA-liposome-treated mice compared to the sham-treated group. In conclusion, in vivo efficacy data showed that prophylactic SLIT with OVA-liposomes is significantly more effective in preventing allergic inflammation than the corresponding dose of free OVA. Keywords: sublingual immunotherapy, drug delivery, allergy, liposome |
format |
article |
author |
Aliu H Rask C Brimnes J Andresen TL |
author_facet |
Aliu H Rask C Brimnes J Andresen TL |
author_sort |
Aliu H |
title |
Enhanced efficacy of sublingual immunotherapy by liposome-mediated delivery of allergen |
title_short |
Enhanced efficacy of sublingual immunotherapy by liposome-mediated delivery of allergen |
title_full |
Enhanced efficacy of sublingual immunotherapy by liposome-mediated delivery of allergen |
title_fullStr |
Enhanced efficacy of sublingual immunotherapy by liposome-mediated delivery of allergen |
title_full_unstemmed |
Enhanced efficacy of sublingual immunotherapy by liposome-mediated delivery of allergen |
title_sort |
enhanced efficacy of sublingual immunotherapy by liposome-mediated delivery of allergen |
publisher |
Dove Medical Press |
publishDate |
2017 |
url |
https://doaj.org/article/8b809d56112c4111a4e1ab7c25129a1f |
work_keys_str_mv |
AT aliuh enhancedefficacyofsublingualimmunotherapybyliposomemediateddeliveryofallergen AT raskc enhancedefficacyofsublingualimmunotherapybyliposomemediateddeliveryofallergen AT brimnesj enhancedefficacyofsublingualimmunotherapybyliposomemediateddeliveryofallergen AT andresentl enhancedefficacyofsublingualimmunotherapybyliposomemediateddeliveryofallergen |
_version_ |
1718403940468391936 |