The effects of anti-sense interleukin-5 gene transferred by recombinant adeno-associated virus in allergic rats
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- Department of Respiratory Medicine, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology
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- Manuscript
- Date:
- Received 03 July 2008 06:19 UTC; Posted 09 July 2008
- Subjects:
- Biotechnology, Molecular Cell Biology
- Abstract:
The accumulation and infiltration of eosinophils in airways is one of the most important characteristics of asthma, and is mediated partly by secretion of IL-5 from Th2 lymphocytes. It is well known that interleukin-5 (IL-5) played an important role in the regulation of eosinophils. In this study, an anti-sense IL-5 gene transferred by recombinant adeno-associated virus (rAAV-ASIL-5) was prepared to transfect allergic rats. It was found that the expression of IL-5 protein in plasma and BALF were inhibited significantly. The rAAV-ASIL-5-mediated suppression of total cell counts in peripheral blood and BALF were also observed. Moreover, rAAV-ASIL-5 remarkably reduced the eosinophil counts in peripheral blood and BALF, as well as the expression of ECP protein in plasma and BALF. The inflammation in lungs of rAAV-ASIL-5 pretreated rats also became slighter when compared with allergic rats. Otherwise, no apparent pathological damage to vital organs of rats was found. In conclusion, recombinant adeno-associated virus-mediated delivery of anti-sense IL-5 gene inhibited the accumulation of eosinophils and the airways inflammation in rat model of allergic asthma via suppressing IL-5 expression. It suggested the feasibility of rAAV-ASIL-5 in the gene therapy for allergic asthma and other eosinophilic diseases.
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- This document is licensed to the public under the Creative Commons Attribution 3.0 License
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Zeng, Daxiong, Cao, Yong, Song, Qingfeng, Cao, Chao, Liu, Xiansheng, Xu, Yongjian, and Xiong, Weining. The effects of anti-sense interleukin-5 gene transferred by recombinant adeno-associated virus in allergic rats. Available from Nature Precedings <http://hdl.handle.net/10101/npre.2008.2036.1> (2008)
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