Predicting the outcomes of treatment to eradicate the latent reservoir for HIV-1

被引:214
作者
Hill, Alison L. [1 ,2 ,3 ,4 ]
Rosenbloom, Daniel I. S. [1 ,2 ,5 ]
Fu, Feng [6 ]
Nowak, Martin A. [1 ,2 ]
Siliciano, Robert F. [7 ,8 ]
机构
[1] Harvard Univ, Dept Math, Program Evolutionary Dynam, Cambridge, MA 02138 USA
[2] Harvard Univ, Dept Organism & Evolutionary Biol, Cambridge, MA 02138 USA
[3] Harvard Univ, Biophys Program, Cambridge, MA 02138 USA
[4] Harvard Univ, Harvard Mit Div Hlth Sci & Technol, Cambridge, MA 02138 USA
[5] Columbia Univ, Med Ctr, Dept Biomed Informat, New York, NY 10032 USA
[6] ETH, Inst Integrat Biol, CH-8092 Zurich, Switzerland
[7] Johns Hopkins Univ, Sch Med, Dept Med, Baltimore, MD 21205 USA
[8] Johns Hopkins Univ, Sch Med, Howard Hughes Med Inst, Baltimore, MD 21205 USA
基金
欧洲研究理事会; 美国国家卫生研究院;
关键词
HIV latent reservoir; HIV cure; viral dynamics; CD4(+) T-CELLS; ANTIRETROVIRAL THERAPY; VIREMIA; ESTABLISHMENT; REPLICATION; INFECTION; INTENSIFICATION; REACTIVATION; PERSISTENCE; BROMODOMAIN;
D O I
10.1073/pnas.1406663111
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Massive research efforts are now underway to develop a cure for HIV infection, allowing patients to discontinue lifelong combination antiretroviral therapy (ART). New latency- reversing agents (LRAs) may be able to purge the persistent reservoir of latent virus in resting memory CD4(+) T cells, but the degree of reservoir reduction needed for cure remains unknown. Here we use a stochastic model of infection dynamics to estimate the efficacy of LRA needed to prevent viral rebound after ART interruption. We incorporate clinical data to estimate population-level parameter distributions and outcomes. Our findings suggest that similar to 2,000-fold reductions are required to permit a majority of patients to interrupt ART for 1 y without rebound and that rebound may occur suddenly after multiple years. Greater than 10,000-fold reductions may be required to prevent rebound altogether. Our results predict large variation in rebound times following LRA therapy, which will complicate clinical management. This model provides benchmarks for moving LRAs from the laboratory to the clinic and can aid in the design and interpretation of clinical trials. These results also apply to other interventions to reduce the latent reservoir and can explain the observed return of viremia after months of apparent cure in recent bone marrow transplant recipients and an immediately-treated neonate.
引用
收藏
页码:13475 / 13480
页数:6
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