Evidence map›Paper›PMID 20041213›Full record

ReviewPLoS pathogens2009

Chemokine coreceptor signaling in HIV-1 infection and pathogenesis.

Yuntao Wu, Alyson Yoder

Abstract readReview
In one paragraph

Review in PLoS pathogens, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 83 papers.

0numbers the graph read from it
0cells of the map it votes in
83citing papers in PubMed
–field-weighted citation impact
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

83 citing papers in PubMed.

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

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

2 authors.

Yuntao WuDepartment of Molecular and Microbiology, George Mason University, Manassas, Virginia, USA. ywu8@gmu.edu
Alyson Yoder

Funding

Regulation of Cofilin in HIV-1 Infection of Human CD4 T CellsR01AI081568 · NIAID · GEORGE MASON UNIVERSITY · PI WU, YUNTAO · 2009 to 2012
$1.2M
Determine the Transcriptional Activity of Non-integrated HIV-1 DNAR21AI069981 · NIAID · GEORGE MASON UNIVERSITY · PI WU, YUNTAO · 2007 to 2008
$340k
NIAID NIH HHS 1R01AI081568NIAID NIH HHS AI069981NIAID NIH HHS R01 AI081568NIAID NIH HHS R21 AI069981
6 · The paper itself

Abstract

Binding of the HIV-1 envelope to its chemokine coreceptors mediates two major biological events: membrane fusion and signaling transduction. The fusion process has been well studied, yet the role of chemokine coreceptor signaling in viral infection has remained elusive through the past decade. With the recent demonstration of the signaling requirement for HIV latent infection of resting CD4 T cells, the issue of coreceptor signaling needs to be thoroughly revisited. It is likely that virus-mediated signaling events may facilitate infection in various immunologic settings in vivo where cellular conditions need to be primed; in other words, HIV may exploit the chemokine signaling network shared among immune cells to gain access to downstream cellular components, which can then serve as effective tools to break cellular barriers. This virus-hijacked aberrant signaling process may in turn facilitate pathogenesis. In this review, we summarize past and present studies on HIV coreceptor signaling. We also discuss possible roles of coreceptor signaling in facilitating viral infection and pathogenesis.

Indexed as

AnimalsHIVHIV InfectionsHumansReceptors, CCR5Receptors, CXCR4Signal TransductionCXCR4 protein, humanReceptors, CCR5Receptors, CXCR4

Identifiers

PMID20041213
PMCPMC2790611

What OpenQuestion holds

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LicenceCC BY
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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.