Evidence map›Paper›PMID 31295427›Full record

ArticleCell host & microbe2019

The Landscape of Persistent Viral Genomes in ART-Treated SIV, SHIV, and HIV-2 Infections.

Alexandra M Bender, Francesco R Simonetti, Mithra R Kumar, Emily J Fray, Katherine M Bruner, Andrew E Timmons, Katherine Y Tai, Katharine M Jenike, Annukka A R Antar, Po-Ting Liu and 14 more

Open access · bronzeAbstract read
In one paragraph

Article in Cell host & microbe, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 84 papers.

0numbers the graph read from it
0cells of the map it votes in
84citing papers in PubMed
7.0field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

84 citing papers in PubMed, 99 citations in OpenAlex.

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24 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

24 authors at 7 institutions in 2 countries.

Alexandra M BenderDepartment of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Francesco R SimonettiDepartment of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Mithra R KumarDepartment of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Emily J FrayDepartment of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Katherine M BrunerDepartment of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Andrew E TimmonsDepartment of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Katherine Y TaiDepartment of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Katharine M JenikeDepartment of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Annukka A R AntarDepartment of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Po-Ting LiuCenter for Virology and Vaccine Research, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02215, USA.
Ya-Chi HoDepartment of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Dana N RaugiDepartment of Medicine & Center of Emerging & Re-Emerging Infectious Diseases, University of Washington, Seattle, WA, USA.
Moussa SeydiService de Maladies Infectieuses et Tropicales, CHNU-Fann, Dakar, Senegal.
Geoffrey S GottliebDepartment of Medicine & Center of Emerging & Re-Emerging Infectious Diseases, University of Washington, Seattle, WA, USA.
Afam A OkoyeVaccine and Gene Therapy Institute, Oregon Health and Sciences University, Beaverton, OR, USA.
Gregory Q Del PreteAIDS and Cancer Virus Program, Frederick National Laboratory, Frederick, MD, USA.
Louis J PickerVaccine and Gene Therapy Institute, Oregon Health and Sciences University, Beaverton, OR, USA.
Joseph L MankowskiDepartment of Molecular and Comparative Pathobiology, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Jeffrey D LifsonAIDS and Cancer Virus Program, Frederick National Laboratory, Frederick, MD, USA.
Janet D SilicianoDepartment of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Greg M LairdDepartment of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA; Accelevir Diagnostics, Baltimore, MD, USA.
Dan H BarouchCenter for Virology and Vaccine Research, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02215, USA.
Janice E ClementsDepartment of Molecular and Comparative Pathobiology, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Robert F SilicianoDepartment of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA; Howard Hughes Medical Institute, Baltimore, MD 21205, USA. Electronic address: rsiliciano@jhmi.edu.
Johns Hopkins University · USBeth Israel Deaconess Medical Center · USChildren's Cancer Therapy Development Institute · USFrederick National Laboratory for Cancer Research · USUniversity of Washington · USCentre Hospitalier National Universitaire de Fann · SNHoward Hughes Medical Institute · US

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
First-in-human study of two anti-SARS CoV-2 antibodies in health volunteersUM1AI126620 · NIAID · WISTAR INSTITUTE · PI MONTANER, LUIS J, RILEY, JAMES L. · 2016 to 2021
$24.5M
BIOCHEMISTRY, CELLULAR AND MOLECULAR BIOLOGY PROGRAMT32GM007445 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI GREEN, RACHEL · 1985 to 2021
$24.1M
Combined Immunologic Approaches to Cure HIV-1UM1AI126603 · NIAID · BETH ISRAEL DEACONESS MEDICAL CENTER · PI BAROUCH, DAN H., MELLORS, JOHN W · 2016 to 2020
$23.6M
Project 4: Intracellular mechanism of virus persistence in astrocytes/macrophagesP01MH070306 · NIMH · JOHNS HOPKINS UNIVERSITY · PI CLEMENTS, JANICE E · 2004 to 2015
$16.0M
RESEARCH TRAINING IN MICROBIAL DISEASEST32AI007291 · NIAID · JOHNS HOPKINS UNIVERSITY · PI JOEL N BLANKSON, Sara Elizabeth Cosgrove · 1986 to 2026
$9.1M
Improving Diagnosis, Treatment & Detection of Drug Resistance in HIV-2 InfectionR01AI120765 · NIAID · UNIVERSITY OF WASHINGTON · PI Geoffrey Scott Gottlieb · 2015 to 2026
$8.9M
Project !: Differential contribution of resting CD4+ T cells and resident macrophages to viral rebound after antiretroviral treatment interruptionP01AI131306 · NIAID · JOHNS HOPKINS UNIVERSITY · PI CLEMENTS, JANICE E, MANKOWSKI, JOSEPH L · 2017 to 2021
$8.5M
Antiretroviral Therapy for HIV-2 Infection in SenegalR01AI060466 · NIAID · UNIVERSITY OF WASHINGTON · PI GOTTLIEB, GEOFFREY SCOTT · 2005 to 2014
$6.5M
Viral Testing CoreU42OD010426 · OD · OREGON HEALTH & SCIENCE UNIVERSITY · PI Andrew Haertel, Lauren Drew Martin · 2013 to 2026
$6.0M
Development of an SPF Macaca nemestrina Breeding ColonyP40OD013117 · OD · JOHNS HOPKINS UNIVERSITY · PI ADAMS, ROBERT J. · 2012 to 2016
$4.9M
Macrophage Ontogeny and Polarization in HIV/SIV InfectionR01AI127142 · NIAID · JOHNS HOPKINS UNIVERSITY · PI CLEMENTS, JANICE E, GAMA, LUCIO · 2016 to 2020
$3.8M
Howard Hughes Medical InstituteNCATS NIH HHS UL1 TR001863NIAID NIH HHS P01 AI131306NIAID NIH HHS R01 AI043222NIAID NIH HHS R01 AI051178NIAID NIH HHS R01 AI060466NIAID NIH HHS R01 AI120765NIAID NIH HHS R01 AI127142NIAID NIH HHS R56 AI118753NIAID NIH HHS T32 AI007291NIAID NIH HHS UM1 AI126603NIAID NIH HHS UM1 AI126620NIGMS NIH HHS T32 GM007445NIH HHS P40 OD013117NIH HHS U42 OD010426NIMH NIH HHS P01 MH070306NINDS NIH HHS R01 NS076357NINDS NIH HHS R01 NS077869
6 · The paper itself

Abstract

Evaluation of HIV cure strategies is complicated by defective proviruses that persist in ART-treated patients but are irrelevant to cure. Non-human primates (NHP) are essential for testing cure strategies. However, the persisting proviral landscape in ART-treated NHPs is uncharacterized. Here, we describe viral genomes persisting in ART-treated, simian immunodeficiency virus (SIV)-infected NHPs, simian-human immunodeficiency virus (SHIV)-infected NHPs, and humans infected with HIV-2, an SIV-related virus. The landscapes of persisting SIV, SHIV, and HIV-2 genomes are also dominated by defective sequences. However, there was a significantly higher fraction of intact SIV proviral genomes compared to ART-treated HIV-1 or HIV-2 infected humans. Compared to humans with HIV-1, SIV-infected NHPs had more hypermutated genomes, a relative paucity of clonal SIV sequences, and a lower frequency of deleted genomes. Finally, we report an assay for measuring intact SIV genomes which may have value in cure research.

Indexed as

Genetic VariationAnimalsAnti-Retroviral AgentsDefective VirusesGenome, ViralHIV-1HIV-2HIV InfectionsHumansMacaca mulattaProvirusesSimian Acquired Immunodeficiency SyndromeSimian Immunodeficiency VirusAnti-Retroviral Agentsclonal expansiondefective provirusHIV-2latent reservoirSHIVSIV

Identifiers

PMID31295427
PMCPMC6724192
OpenAlexW2958952516

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.