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dc.contributor.author이민형-
dc.date.accessioned2019-12-03T02:38:35Z-
dc.date.available2019-12-03T02:38:35Z-
dc.date.issued2017-12-
dc.identifier.citationGENE THERAPY, v. 24, no. 11, page. 727-734en_US
dc.identifier.issn0969-7128-
dc.identifier.issn1476-5462-
dc.identifier.urihttps://www.nature.com/articles/gt201783-
dc.identifier.urihttps://repository.hanyang.ac.kr/handle/20.500.11754/116723-
dc.description.abstractAsthma is a multifactorial disease that is influenced by the interaction of genetic and environmental factors. Because of its complex nature, there is no cure for asthma currently. Instead, reliever and controller medications are used to treat asthma. Unfortunately, conventional treatments do not work in some severe cases of asthma. In addition, there may be adverse, systemic effects of long-term treatment with high-dose inhaled corticosteroids (ICSs) as a controller medication. Therefore, we attempted to develop a novel combination therapy for asthma. Our regimen included dexamethasone as a controller medication and vitamin D binding protein (VDBP) small interfering RNA (siRNA) as a novel target therapeutic. The dexamethasone moiety of DEXA-PEI (dexamethasone-conjugated polyethylenimine) was used as an ICS, combined with anti-VDBP treatment via delivery of VDBP siRNA, using DEXA-PEI as a siRNA carrier molecule. Treatment with DEXA-PEI/VDBP siRNA effectively reduced the ovalbumin sensitization/challenge-induced enhancement of airway inflammation, goblet cell hyperplasia and expression of interleukin (IL)-4, IL-13 and CCL11. These findings suggest that the DEXA-PEI/VDBP siRNA can be developed as a potent asthma therapeutic by dose-reducing ICSs and using a multitarget therapeutic method.en_US
dc.description.sponsorshipThis work was supported by the National Research Foundation of Korea (NRF) grant funded by the Korea government (MSIP) (No. NRF-2014R1A2A2A01006740). MC was partly supported by NRF-2012M3A9D1054451.en_US
dc.language.isoen_USen_US
dc.publisherNATURE PUBLISHING GROUPen_US
dc.subjectRANDOMIZED CONTROLLED-TRIALen_US
dc.subjectAIRWAY INFLAMMATIONen_US
dc.subjectGENE CARRIERen_US
dc.subjectPLASMID DNAen_US
dc.subjectSTRATEGYen_US
dc.subjectDELIVERYen_US
dc.subjectPARTICLEen_US
dc.subjectIL-13en_US
dc.titleA new combination therapy for asthma using dual-function dexamethasone-conjugated polyethylenimine and vitamin D binding protein siRNAen_US
dc.typeArticleen_US
dc.relation.no11-
dc.relation.volume24-
dc.identifier.doi10.1038/gt.2017.83-
dc.relation.page727-734-
dc.relation.journalGENE THERAPY-
dc.contributor.googleauthorChoi, M.-
dc.contributor.googleauthorGu, J.-
dc.contributor.googleauthorLee, M.-
dc.contributor.googleauthorRhim, T.-
dc.relation.code2017001536-
dc.sector.campusS-
dc.sector.daehakCOLLEGE OF ENGINEERING[S]-
dc.sector.departmentDEPARTMENT OF BIOENGINEERING-
dc.identifier.pidminhyung-
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COLLEGE OF ENGINEERING[S](공과대학) > BIOENGINEERING(생명공학과) > Articles
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