作者: Joep M. A. Lange , Julio S. G. Montaner
DOI: 10.1007/978-94-017-0685-8_13
关键词: Drug 、 Human immunodeficiency virus (HIV) 、 Acquired immunodeficiency syndrome (AIDS) 、 Zidovudine 、 Reverse transcriptase 、 Nucleoside analogue 、 Lymphocyte 、 Opportunistic infection 、 Virology 、 Medicine
摘要: The era of anti-retroviral therapy starts in 1986. Only three years after the now so designated human immunodeficiency virus (HIV) was identified as causative agent acquired immunodeficency syndrome (AIDS), treatment with zidovudine (3’-azido-3’-deoxythymidine, AZT, ZDV), a nucleoside analogue inhibitor viral reverse transcriptase (RT), shown to significantly reduce mortality patients advanced HIV-1 infection, which paralelled by rise CD4+ lymphocyte counts [1]. also appeared confer benefits less infection [2–4]. Initial high hopes for this drug, however, led subsequent disappointment when, extended follow-up, its effects on morbidity and proved be limited duration [5,6].