Evidence map›Paper›PMID 33377133›Full record

ArticleCell reports. Medicine2020

Tracking HIV Rebound following Latency Reversal Using Barcoded HIV.

Matthew D Marsden, Tian-Hao Zhang, Yushen Du, Melanie Dimapasoc, Mohamed S A Soliman, Xiaomeng Wu, Jocelyn T Kim, Akira Shimizu, Adam Schrier, Paul A Wender and 2 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports. Medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

24 citing papers in PubMed, 31 citations in OpenAlex.

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  11. The Complex Dysregulations of CD4 T Cell Subtypes in HIV Infection.International journal of molecular sciences · 2024
    Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 3 institutions in 2 countries.

Matthew D MarsdenDepartment of Microbiology and Molecular Genetics and Department of Medicine, Division of Infectious Diseases, School of Medicine, University of California, Irvine, Irvine, CA 92697, USA.
Tian-Hao ZhangMolecular Biology Institute, University of California, Los Angeles, Los Angeles, CA 90095, USA.
Yushen DuDepartment of Molecular and Medical Pharmacology, University of California, Los Angeles, Los Angeles, CA 90095, USA.
Melanie DimapasocDepartment of Microbiology, Immunology, and Molecular Genetics, University of California, Los Angeles, Los Angeles, CA 90095, USA.
Mohamed S A SolimanDepartment of Microbiology, Immunology, and Molecular Genetics, University of California, Los Angeles, Los Angeles, CA 90095, USA.
Xiaomeng WuDepartment of Microbiology, Immunology, and Molecular Genetics, University of California, Los Angeles, Los Angeles, CA 90095, USA.
Jocelyn T KimDepartment of Medicine, Division of Infectious Diseases, University of California, Los Angeles, Los Angeles, CA 90095, USA.
Akira ShimizuDepartments of Chemistry and Chemical and Systems Biology, Stanford University, Stanford, CA 94305, USA.
Adam SchrierDepartments of Chemistry and Chemical and Systems Biology, Stanford University, Stanford, CA 94305, USA.
Paul A WenderDepartments of Chemistry and Chemical and Systems Biology, Stanford University, Stanford, CA 94305, USA.
Ren SunDepartment of Molecular and Medical Pharmacology, University of California, Los Angeles, Los Angeles, CA 90095, USA.
Jerome A ZackDepartment of Microbiology, Immunology, and Molecular Genetics, University of California, Los Angeles, Los Angeles, CA 90095, USA.
University of California, Los Angeles · USStanford University · USUniversity of California, Irvine · US

Funding

UCLA Clinical Translational Science InstituteUL1TR001881 · NCATS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI ARLEEN F. BROWN, ARASH NAEIM · 2016 to 2026
$118.1M
UCLA Clinical and Translational Science InstituteUL1TR000124 · NCATS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI DUBINETT, STEVEN M. · 2012 to 2015
$57.0M
Virology CoreP30AI028697 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI KITCHEN, SCOTT G · 1991 to 2018
$39.9M
UCLA NIGMS T32 Program AssessmentT32GM007185 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI TORRES, JORGE · 1985 to 2020
$21.7M
UCLA Tumor Immunology Training ProgramT32CA009120 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Steven M. Dubinett, MICHAEL A TEITELL · 1985 to 2026
$10.3M
Viral Genetics CoreP01AI131294 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI DU, YUSHENG · 2017 to 2021
$7.5M
SYNTHETIC STUDIES RELATED TO CANCER RESEARCH/TREATMENTR01CA031845 · NCI · STANFORD UNIVERSITY · PI PAUL Anthony WENDER · 1985 to 2026
$6.9M
Synthetic Studies Related to Cancer Research/TreatmentR37CA031845 · NCI · STANFORD UNIVERSITY · PI WENDER, PAUL ANTHONY · 2006 to 2015
$4.5M
HIV latency reversal through novel, potent PKC modulatorsR01AI124743 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI WENDER, PAUL ANTHONY, ZACK, JEROME A. · 2016 to 2020
$3.3M
The Effect of Natural Killer Cell-Based Therapy on the HIV ReservoirK08AI155232 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI KIM, JOCELYN T · 2020 to 2024
$1.0M
HIV Latency Reversal Through Novel, Potent PKC ModulatorsR56AI124743 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI WENDER, PAUL ANTHONY, ZACK, JEROME A. · 2021 to 2021
$798k
Novel method for evaluating HIV latency and persistence in vivoR21AI124763 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI MARSDEN, MATTHEW DAVID · 2016 to 2017
$424k
NCATS NIH HHS UL1 TR000124NCATS NIH HHS UL1 TR001881NCI NIH HHS R01 CA031845NCI NIH HHS R37 CA031845NCI NIH HHS T32 CA009120NIAID NIH HHS K08 AI155232NIAID NIH HHS P01 AI131294NIAID NIH HHS P30 AI028697NIAID NIH HHS R01 AI124743NIAID NIH HHS R21 AI124763NIAID NIH HHS R56 AI124743NIGMS NIH HHS T32 GM007185
6 · The paper itself

Abstract

HIV latency prevents cure of infection with antiretroviral therapy (ART) alone. One strategy for eliminating latently infected cells involves the induction of viral protein expression via latency-reversing agents (LRAs), allowing killing of host cells by viral cytopathic effects or immune effector mechanisms. Here, we combine a barcoded HIV approach and a humanized mouse model to study the effects of a designed, synthetic protein kinase C modulating LRA on HIV rebound. We show that administration of this compound during ART results in a delay in rebound once ART is stopped. Furthermore, the rebounding virus appears composed of a smaller number of unique barcoded viruses than occurs in control-treated animals, suggesting that some reservoir cells that would have contributed virus to the rebound process are eliminated by LRA administration. These data support the use of barcoded virus to study rebound and suggest that LRAs may be useful in HIV cure efforts.

Indexed as

AnimalsAnti-HIV AgentsCD4-Positive T-LymphocytesHIV-1HIV InfectionsHumansMiceProtein Kinase CVirus ActivationVirus LatencyVirus ReplicationAnti-HIV AgentsProtein Kinase Cantiretroviral therapyARTcureHIVhumanized micelatencyLRAprotein kinase Creservoir

Identifiers

PMID33377133
PMCPMC7762775
OpenAlexW3114900214

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.