TY - JOUR
T1 - Distinct viral reservoirs in individuals with spontaneous control of HIV-1
AU - Jiang, Chenyang
AU - Lian, Xiaodong
AU - Gao, Ce
AU - Sun, Xiaoming
AU - Einkauf, Kevin B.
AU - Chevalier, Joshua M.
AU - Chen, Samantha M.Y.
AU - Hua, Stephane
AU - Rhee, Ben
AU - Chang, Kaylee
AU - Blackmer, Jane E.
AU - Osborn, Matthew
AU - Peluso, Michael J.
AU - Hoh, Rebecca
AU - Somsouk, Ma
AU - Milush, Jeffrey
AU - Bertagnolli, Lynn N.
AU - Sweet, Sarah E.
AU - Varriale, Joseph A.
AU - Burbelo, Peter D.
AU - Chun, Tae Wook
AU - Laird, Gregory M.
AU - Serrao, Erik
AU - Engelman, Alan N.
AU - Carrington, Mary
AU - Siliciano, Robert F.
AU - Siliciano, Janet M.
AU - Deeks, Steven G.
AU - Walker, Bruce D.
AU - Lichterfeld, Mathias
AU - Yu, Xu G.
N1 - Funding Information:
Acknowledgements X.G.Y. is supported by NIH grants HL134539, AI116228, AI078799, DA047034 and the Bill and Melinda Gates Foundation (INV-002703). M.L. is supported by NIH grants AI098487, AI135940, AI114235, AI117841, AI120008 and DK120387. M.L. and X.G.Y. are Associated Members of the BEAT-HIV Martin Delaney Collaboratory (UM1 AI126620). A.N.E. is supported by NIH grant AI052014. Support was also provided by the Harvard University (HU) and University of California at San Francisco (UCSF)/Gladstone Institute for HIV Cure Research Centers for AIDS Research (P30 AI060354 and P30 AI027763, respectively), which are supported by the following institutes and centers that are co-funded by and associated with the US National Institutes of Health: NIAID, NCI, NICHD, NHLBI, NIDA, NIMH, NIA, FIC and OAR, and by HU CFAR Developmental Awards (S.H.). We thank the MGH DNA core facility. R.F.S. and J.M.S. are supported by the NIH Martin Delaney I4C (UM1 AI126603), BEAT-HIV (UM1 AI126620) and the Delaney AIDS Research Enterprise (DARE; UM1 AI126611) Collaboratories and by the Howard Hughes Medical Institute and the Bill and Melinda Gates Foundation (OPP1115715). Additional support for the SCOPE cohort was provided by DARE (AI096109 and AI127966) and the amfAR Institute for HIV Cure Research (amfAR 109301). G.M.L. is supported by NSF grant 1738428 and NIH grant R44AI124996. The International HIV Controller Cohort is supported by the Bill and Melinda Gates Foundation (OPP1066973), the Ragon Institute of MGH, MIT and Harvard, the NIH (R37 AI067073 to B.D.W.) and the Mark and Lisa Schwartz Family Foundation. This project has been funded in whole or in part with federal funds from the Frederick National Laboratory for Cancer Research, under contract no. HHSN261200800001E. This research was supported in part by the Intramural Research Program of the NIH, Frederick National Lab, Center for Cancer Research and Intramural Programs of NIDCR, NIH. The content of this publication does not necessarily reflect the views or policies of the Department of Health and Human Services, nor does mention of trade names, commercial products, or organizations imply endorsement by the US Government.
Publisher Copyright:
© 2020, The Author(s), under exclusive licence to Springer Nature Limited.
PY - 2020/9/10
Y1 - 2020/9/10
N2 - 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 reservoir1. 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 Krüppel-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 transplantation2,3, may be feasible in rare instances.
AB - 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 reservoir1. 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 Krüppel-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 transplantation2,3, may be feasible in rare instances.
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U2 - 10.1038/s41586-020-2651-8
DO - 10.1038/s41586-020-2651-8
M3 - Article
C2 - 32848246
AN - SCOPUS:85089867477
SN - 0028-0836
VL - 585
SP - 261
EP - 267
JO - Nature
JF - Nature
IS - 7824
ER -