Evidence map›Paper›PMID 34287053›Full record

ArticleJournal of virology2021

Th17 T Cells and Immature Dendritic Cells Are the Preferential Initial Targets after Rectal Challenge with a Simian Immunodeficiency Virus-Based Replication-Defective Dual-Reporter Vector.

Danijela Maric, Wesley A Grimm, Natalie Greco, Michael D McRaven, Angela J Fought, Ronald S Veazey, Thomas J Hope

Open access · greenAbstract read
In one paragraph

Article in Journal of virology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.6field-weighted citation impact, top 19% 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

12 citing papers in PubMed, 12 citations in OpenAlex.

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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

7 authors at 2 institutions in 1 country.

Danijela MaricNorthwestern Universitygrid.16753.36 Feinberg School of Medicine, Department of Cell and Developmental Biology, Chicago, Illinois, USA.
Wesley A GrimmNorthwestern Universitygrid.16753.36 Feinberg School of Medicine, Department of Cell and Developmental Biology, Chicago, Illinois, USA.
Natalie GrecoNorthwestern Universitygrid.16753.36 Feinberg School of Medicine, Department of Cell and Developmental Biology, Chicago, Illinois, USA.
Michael D McRavenNorthwestern Universitygrid.16753.36 Feinberg School of Medicine, Department of Cell and Developmental Biology, Chicago, Illinois, USA.
Angela J FoughtNorthwestern Universitygrid.16753.36 Feinberg School of Medicine, Department of Cell and Developmental Biology, Chicago, Illinois, USA.
Ronald S VeazeyTulane National Primate Research Center, Division of Comparative Pathology, Covington, Louisiana, USA.
Thomas J HopeNorthwestern Universitygrid.16753.36 Feinberg School of Medicine, Department of Cell and Developmental Biology, Chicago, Illinois, USA.ORCID 0000-0001-7183-8319
Northwestern University · USTulane University · US

Funding

Tulane NPRC SPF Sheltered Outdoor Enclosure ExpansionP51OD011104 · OD · TULANE UNIVERSITY OF LOUISIANA · PI L Lee HAMM · 2012 to 2026
$142.4M
Virology and Immunology Technology CoreP30AI117943 · NIAID · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Sahera Dirajlal-Fargo · 2015 to 2026
$38.4M
Sustained Long Acting Prevention Against HIV Program OperationUM1AI120184 · NIAID · NORTHWESTERN UNIVERSITY AT CHICAGO · PI HOPE, THOMAS, KISER, PATRICK FRANKLIN · 2015 to 2019
$17.9M
Identification of the Initial Targets of Transmission R37AI094595 · NIAID · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Thomas Hope · 2017 to 2026
$10.0M
Identification of the Initial Targets of TransmissionR01AI094595 · NIAID · NORTHWESTERN UNIVERSITY AT CHICAGO · PI HOPE, THOMAS · 2011 to 2015
$4.5M
Third Coast HIV-Related Cardiovascular and Sleep Disorders K12 Career Development ProgramK12HL143959 · NHLBI · UNIVERSITY OF CHICAGO · PI ARDEHALI, HOSSEIN, SCHNEIDER, JOHN · 2018 to 2022
$1.5M
HHS | NIH | National Institute of Allergy and Infectious Diseases (NIAID) AI094595HHS | NIH | National Institute of Allergy and Infectious Diseases (NIAID) UM1AI120184NHLBI NIH HHS K12 HL143959NIAID NIH HHS P30 AI117943NIAID NIH HHS R01 AI094595NIAID NIH HHS R37 AI094595NIAID NIH HHS UM1 AI120184NIH HHS P51 OD011104
6 · The paper itself

Abstract

Understanding the earliest events of human immunodeficiency virus (HIV) sexual transmission is critical to developing and optimizing HIV prevention strategies. To gain insights into the earliest steps of HIV rectal transmission, including cellular targets, rhesus macaques were intrarectally challenged with a single-round simian immunodeficiency virus (SIV)-based dual reporter that expresses luciferase and near-infrared fluorescent protein 670 (iRFP670) upon productive transduction. The vector was pseudotyped with the HIV-1 envelope JRFL. Regions of tissue containing foci of luminescent transduced cells were identified macroscopically using an

Indexed as

Anal CanalAnimalsDendritic CellsFemaleHIV-1HIV InfectionsIntestinal MucosaMacaca mulattaRectumSimian Acquired Immunodeficiency SyndromeSimian Immunodeficiency VirusTh17 CellsVirus ReplicationHIV/SIV transmissioniDCsrectal mucosarhesus macaqueTh17 T cells

Identifiers

PMID34287053
PMCPMC8428389
OpenAlexW3183696212

What OpenQuestion holds

Textmetadata
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.