Thermosensitive PLGA-PEG-PLGA Hydrogel as Depot Matrix for Allergen-Specific Immunotherapy

被引:10
作者
Heine, Sonja [1 ,2 ]
Aguilar-Pimentel, Antonio [3 ]
Russkamp, Dennis [1 ,2 ]
Alessandrini, Francesca [1 ,2 ]
Gailus-Durner, Valerie [3 ]
Fuchs, Helmut [3 ]
Ollert, Markus [4 ,5 ]
Bredehorst, Reinhard [6 ]
Ohnmacht, Caspar [1 ,2 ]
Zissler, Ulrich M. [1 ,2 ]
Hrabe de Angelis, Martin [3 ,7 ,8 ]
Schmidt-Weber, Carsten B. [1 ,2 ]
Blank, Simon [1 ,2 ]
机构
[1] Tech Univ Munich, Sch Med, Ctr Allergy & Environm ZAUM, D-85764 Munich, Germany
[2] German Res Ctr Environm Hlth, Helmholtz Ctr Munich, D-85764 Munich, Germany
[3] German Res Ctr Environm Hlth, Helmholtz Ctr Munich, Inst Expt Genet, German Mouse Clin, D-85764 Neuherberg, Germany
[4] Luxembourg Inst Hlth LIH, Dept Infect & Immun, L-4354 Esch Sur Alzette, Luxembourg
[5] Univ Southern Denmark, Odense Res Ctr Anaphylaxis, Dept Dermatol & Allergy Ctr, DK-5000 Odense, Denmark
[6] Univ Hamburg, Inst Biochem & Mol Biol, D-20146 Hamburg, Germany
[7] Tech Univ Munich, Sch Life Sci Weihenstephan, Chair Expt Genet, D-85354 Freising Weihenstephan, Germany
[8] German Ctr Diabet Res DZD, D-85764 Neuherberg, Germany
关键词
allergen-specific immunotherapy; allergic asthma; antigen release; hydrogel; delivery system; depot matrix; GRASS-POLLEN IMMUNOTHERAPY; IN-VIVO; SUBCUTANEOUS IMMUNOTHERAPY; ALUMINUM; MECHANISMS; ADJUVANT; CELLS; COPOLYMERS; ANTIBODIES; INDUCTION;
D O I
10.3390/pharmaceutics14081527
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Allergen-specific immunotherapy (AIT) is the only currently available curative treatment option for allergic diseases. AIT often includes depot-forming and immunostimulatory adjuvants, to prolong allergen presentation and to improve therapeutic efficacy. The use of aluminium salts in AIT, which are commonly used as depot-forming adjuvants, is controversially discussed, due to health concerns and Th2-promoting activity. Therefore, there is the need for novel delivery systems in AIT with similar therapeutic efficacy compared to classical AIT strategies. In this study, a triblock copolymer (hydrogel) was assessed as a delivery system for AIT in a murine model of allergic asthma. We show that the hydrogel combines the advantages of both depot function and biodegradability at the same time. We further demonstrate the suitability of hydrogel to release different bioactive compounds in vitro and in vivo. AIT delivered with hydrogel reduces key parameters of allergic inflammation, such as inflammatory cell infiltration, mucus hypersecretion, and allergen-specific IgE, in a comparable manner to standard AIT treatment. Additionally, hydrogel-based AIT is superior in inducing allergen-specific IgG antibodies with potentially protective functions. Taken together, hydrogel represents a promising delivery system for AIT that is able to combine therapeutic allergen administration with the prolonged release of immunomodulators at the same time.
引用
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页数:16
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