Distinct viral reservoirs in individuals with spontaneous control of HIV-1

被引:279
作者
Jiang, Chenyang [1 ,2 ]
Lian, Xiaodong [1 ,2 ]
Gao, Ce [1 ]
Sun, Xiaoming [1 ]
Einkauf, Kevin B. [1 ,2 ]
Chevalier, Joshua M. [1 ,2 ]
Chen, Samantha M. Y. [1 ]
Hua, Stephane [1 ]
Rhee, Ben [1 ,2 ]
Chang, Kaylee [1 ]
Blackmer, Jane E. [1 ]
Osborn, Matthew [1 ]
Peluso, Michael J. [3 ]
Hoh, Rebecca [3 ]
Somsouk, Ma [3 ]
Milush, Jeffrey [3 ]
Bertagnolli, Lynn N. [4 ]
Sweet, Sarah E. [4 ]
Varriale, Joseph A. [4 ]
Burbelo, Peter D. [5 ]
Chun, Tae-Wook [6 ]
Laird, Gregory M. [7 ]
Serrao, Erik [8 ,9 ]
Engelman, Alan N. [8 ,9 ]
Carrington, Mary [1 ,10 ]
Siliciano, Robert F. [4 ,11 ]
Siliciano, Janet M. [4 ,11 ]
Deeks, Steven G. [3 ]
Walker, Bruce D. [1 ,11 ,12 ,13 ]
Lichterfeld, Mathias [1 ,2 ,14 ]
Yu, Xu G. [1 ,2 ]
机构
[1] Ragon Inst MGH MIT & Harvard, Cambridge, MA 02139 USA
[2] Brigham & Womens Hosp, Infect Dis Div, 75 Francis St, Boston, MA 02115 USA
[3] Univ Calif San Francisco, Dept Med, San Francisco, CA 94143 USA
[4] Johns Hopkins Univ, Sch Med, Dept Med, Baltimore, MD 21205 USA
[5] Natl Inst Dent & Craniofacial Res, Dent Clin Res Core, NIH, Bethesda, MD USA
[6] NIAID, 9000 Rockville Pike, Bethesda, MD 20892 USA
[7] Accelevir Diagnost, Baltimore, MD USA
[8] Dana Farber Canc Inst, Dept Canc Immunol & Virol, Boston, MA 02115 USA
[9] Harvard Med Sch, Dept Med, Boston, MA 02115 USA
[10] Frederick Natl Lab Canc Res, Basic Sci Program, Frederick, MD USA
[11] Howard Hughes Med Inst, Chevy Chase, MD USA
[12] MIT, Inst Med Engn & Sci, 77 Massachusetts Ave, Cambridge, MA 02139 USA
[13] MIT, Dept Biol, Cambridge, MA 02139 USA
[14] Broad Inst MIT & Harvard, Cambridge, MA 02142 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
IMMUNODEFICIENCY-VIRUS TYPE-1; CD4(+) T-CELLS; GENE-EXPRESSION; INTACT HIV-1; HUMAN GENOME; INTEGRATION; LATENT; PROVIRUSES; INFECTION; ALIGNMENT;
D O I
10.1038/s41586-020-2651-8
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
Sustained, drug-free control of HIV-1 replication is naturally achieved in less than 0.5% of infected individuals (here termed 'elite controllers'), despite the presence of a replication-competent viral reservoir(1). Inducing such an ability to spontaneously maintain undetectable plasma viraemia is a major objective of HIV-1 cure research, but the characteristics of proviral reservoirs in elite controllers remain to be determined. Here, using next-generation sequencing of near-full-length single HIV-1 genomes and corresponding chromosomal integration sites, we show that the proviral reservoirs of elite controllers frequently consist of oligoclonal to near-monoclonal clusters of intact proviral sequences. In contrast to individuals treated with long-term antiretroviral therapy, intact proviral sequences from elite controllers were integrated at highly distinct sites in the human genome and were preferentially located in centromeric satellite DNA or in Kruppel-associated box domain-containing zinc finger genes on chromosome 19, both of which are associated with heterochromatin features. Moreover, the integration sites of intact proviral sequences from elite controllers showed an increased distance to transcriptional start sites and accessible chromatin of the host genome and were enriched in repressive chromatin marks. These data suggest that a distinct configuration of the proviral reservoir represents a structural correlate of natural viral control, and that the quality, rather than the quantity, of viral reservoirs can be an important distinguishing feature for a functional cure of HIV-1 infection. Moreover, in one elite controller, we were unable to detect intact proviral sequences despite analysing more than 1.5 billion peripheral blood mononuclear cells, which raises the possibility that a sterilizing cure of HIV-1 infection, which has previously been observed only following allogeneic haematopoietic stem cell transplantation(2,3), may be feasible in rare instances. In individuals who have achieved natural control of HIV-1 without drug treatment, intact proviral sequences are integrated into genomic regions that are not permissive to active viral transcription, indicating deep latency of the virus.
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页码:261 / +
页数:22
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