Evidence map›Paper›PMID 19197360›Full record

ArticlePLoS pathogens2009

Differences in APOBEC3G expression in CD4+ T helper lymphocyte subtypes modulate HIV-1 infectivity.

Michael L Vetter, Megan E Johnson, Amanda K Antons, Derya Unutmaz, Richard T D'Aquila

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

30 citing papers in PubMed, 45 citations in OpenAlex.

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  6. The von Hippel-Lindau Cullin-RING E3 ubiquitin ligase regulates APOBEC3 cytidine deaminases.Translational research : the journal of laboratory and clinical medicine · 2021
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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

5 authors at 2 institutions in 1 country.

Michael L VetterDepartment of Microbiology and Immunology, Vanderbilt University, Nashville, TN, USA.
Megan E Johnson
Amanda K Antons
Derya Unutmaz
Richard T D'Aquila
Vanderbilt University · USNew York University · US

Funding

NUCLEOSIDE RESISTANCE OF THE HIV-1 REVERSE TRANSCRIPTASER01AI029193 · NIAID · VANDERBILT UNIVERSITY · PI D'AQUILA, RICHARD T · 1990 to 2007
$2.8M
T Cell Activation Signals That Regulate HIV-1 InfectionR01AI049131 · NIAID · VANDERBILT UNIVERSITY · PI UNUTMAZ, DERYA · 2001 to 2005
$1.6M
HIV/AIDS Research Training ProgramT32AI060571 · NIAID · VANDERBILT UNIVERSITY · PI AIKEN, CHRISTOPHER R · 2004 to 2008
$1.1M
NIAID NIH HHS R01 AI049131NIAID NIH HHS R01 AI29193NIAID NIH HHS R01 AI49131NIAID NIH HHS T32 AI060571
6 · The paper itself

Abstract

The cytidine deaminases APOBEC3G and APOBEC3F exert anti-HIV-1 activity that is countered by the HIV-1 vif protein. Based on potential transcription factor binding sites in their putative promoters, we hypothesized that expression of APOBEC3G and APOBEC3F would vary with T helper lymphocyte differentiation. Naive CD4+ T lymphocytes were differentiated to T helper type 1 (Th1) and 2 (Th2) effector cells by expression of transcription factors Tbet and GATA3, respectively, as well as by cytokine polarization. APOBEC3G and APOBEC3F RNA levels, and APOBEC3G protein levels, were higher in Th1 than in Th2 cells. T cell receptor stimulation further increased APOBEC3G and APOBEC3F expression in Tbet- and control-transduced, but not in GATA3-transduced, cells. Neutralizing anti-interferon-gamma antibodies reduced both basal and T cell receptor-stimulated APOBEC3G and APOBEC3F expression in Tbet- and control-transduced cells. HIV-1 produced from Th1 cells had more virion APOBEC3G, and decreased infectivity, compared to virions produced from Th2 cells. These differences between Th1- and Th2-produced virions were greater for viruses lacking functional vif, but also seen with vif-positive viruses. Over-expression of APOBEC3G in Th2 cells decreased the infectivity of virions produced from Th2 cells, and reduction of APOBEC3G in Th1 cells increased infectivity of virions produced from Th1 cells, consistent with a causal role for APOBEC3G in the infectivity difference. These results indicate that APOBEC3G and APOBEC3F levels vary physiologically during CD4+ T lymphocyte differentiation, that interferon-gamma contributes to this modulation, and that this physiological regulation can cause changes in infectivity of progeny virions, even in the presence of HIV-1 vif.

Indexed as

Gene Expression RegulationAPOBEC-3G DeaminaseCytidine DeaminaseCytosine DeaminaseFlow CytometryGATA3 Transcription FactorHIV-1HumansInterferon-gammaTh1 CellsTh2 CellsTranscription Factorsvif Gene Products, Human Immunodeficiency VirusVirionAPOBEC3F protein, humanAPOBEC-3G DeaminaseAPOBEC3G protein, humanCytidine DeaminaseCytosine DeaminaseGATA3 Transcription FactorInterferon-gammaTranscription Factorsvif Gene Products, Human Immunodeficiency Virusvif protein, Human immunodeficiency virus 1

Identifiers

PMID19197360
PMCPMC2631133
OpenAlexW1988580233

What OpenQuestion holds

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LicenceCC BY
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.