Clinical Trials of Gene Therapy Using anti-HIV RNA

来源 :2005 WHTS3rd Annual Congress of International Drug Discovery | 被引量 : 0次 | 上传用户:huishouzhong2
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  There is no cure for AIDS at this time, although, highly active antiretroviral therapy (HAART) has greatly improved the outcome of HIV/AIDS, it is limited by side effects, viral drug-resistant, and the cost of the therapy.Gene Therapy for HIV/AIDS is suggested as a goal worth considering, and the history and current status of gene therapy for HIV/AIDS will be discussed.A diverse array of transgenes has been developed to inhibit HIV-1 replication and/or protect cells from infection.These are categorized into two types: RNA strategies (antisense, ribozyme [RZ], RNA aptamers, RNA decoys and RNA interference [RNAi]) and protein strategies (transdominant negative mutants, intrakines, toxins, single chain antibodies, and DNA-based vaccines).These can be generally delivered is two ways: in T cells and in hematopoietic progenitor cells (HPC).
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