4.8 Article

Adeno-Associated Virus Delivery of Anti-HIV Monoclonal Antibodies Can Drive Long-Term Virologic Suppression

期刊

IMMUNITY
卷 50, 期 3, 页码 567-+

出版社

CELL PRESS
DOI: 10.1016/j.immuni.2019.02.005

关键词

-

资金

  1. National Institutes of Health (NIH) [P01 AI100263, R01 AI098446, U19 AI0595985]
  2. P51 base grant (Wisconsin National Primate Research Center) from the NIH [RR000167]
  3. Miami Center for AIDS Research
  4. University of Miami Miller School of Medicine from the NIH [P30AI073961]
  5. National Cancer Institute, NIH [HHSN261200800001E]

向作者/读者索取更多资源

Long-term delivery of anti-HIV monoclonal antibodies (mAbs) using adeno-associated virus (AAV) vectors holds promise for the prevention and treatment of HIV infection. We describe a therapy trial in which four rhesus monkeys were infected with SHIV-AD8 for 86 weeks before receiving the AAV-encoded mAbs 3BNC117, 10-1074, and 10E8. Although anti-drug antibody (ADA) responses restricted mAb delivery, one monkey successfully maintained 50-150 mu g/mL of 3BNC117 and 10-1074 for over 2 years. Delivery of these two mAbs to this monkey resulted in an abrupt decline in plasma viremia, which remained undetectable for 38 successive measurements over 3 years. We generated two more examples of virologic suppression using AAV delivery of a cocktail of four mAbs in a 12-monkey study. Our results provide proof of concept for AAV-delivered mAbs to produce a functional cure. However, they also serve as a warning that ADAs may be a problem for practical application of this approach in humans.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据