Butera S T
HIV and Retrovirology Branch, Division of AIDS, STD, and TB Laboratory Research, National Center for Infectious Diseases, Centers for Disease Control and Prevention, Atlanta, GA 30333, USA.
Antiviral Res. 2000 Dec;48(3):143-76. doi: 10.1016/s0166-3542(00)00133-9.
Factors affecting HIV-1 latency present formidable obstacles for therapeutic intervention. As these obstacles have become a clinical reality, even with the use of potent anti-retroviral regimens, the need for novel therapeutic strategies specifically targeting HIV-1 latency is evident. However, therapeutic targeting of HIV-1 latency requires an understanding of the mechanisms regulating viral quiescence and activation. These mechanisms have been partially delineated using chronically infected cell models and, clearly, HIV-1 activation from latency involves several key viral and cellular components. Among these distinctive therapeutic targets, cellular factors involved in HIV-1 transcription especially warrant further consideration for rational drug design. Exploring the scientific possibilities of new therapies targeting HIV-1 latency may hold new promise of eventual HIV-1 eradication.
影响HIV-1潜伏的因素给治疗干预带来了巨大障碍。尽管使用了强效抗逆转录病毒疗法,但这些障碍已成为临床现实,因此显然需要针对HIV-1潜伏的新型治疗策略。然而,针对HIV-1潜伏进行治疗需要了解调节病毒静止和激活的机制。这些机制已通过慢性感染细胞模型得到部分阐明,并且很明显,HIV-1从潜伏状态激活涉及几个关键的病毒和细胞成分。在这些独特的治疗靶点中,参与HIV-1转录的细胞因子尤其值得在合理药物设计中进一步考虑。探索针对HIV-1潜伏的新疗法的科学可能性可能为最终根除HIV-1带来新希望。