慢病毒
遗传增强
病毒载体
逆转录病毒
载体(分子生物学)
基因治疗载体
生物生产
计算生物学
生物
病毒学
重组DNA
病毒
基因传递
生物技术
基因
人类免疫缺陷病毒(HIV)
遗传学
病毒性疾病
作者
María Mercedes Segura,Mathias Mangion,Bruno Gaillet,Alain Garnier
标识
DOI:10.1517/14712598.2013.779249
摘要
The principal hurdles toward the use of recombinant lentivirus as a gene therapy vector are the low titer at which it is produced as well as the difficulty to purify it at an acceptable level without degrading it. The recent advances in the bioproduction of this vector suggest these issues are about to be resolved, making the retrovirus gene therapy a mature technology.
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