Evidence map›Paper›PMID 10400765›Full record

ArticleJournal of virology1999

Patterns of chemokine receptor fusion cofactor utilization by human immunodeficiency virus type 1 variants from the lungs and blood.

A Singh, G Besson, A Mobasher, R G Collman

Open access · bronzeAbstract read
In one paragraph

Article in Journal of virology, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.0field-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

22 citing papers in PubMed, 68 citations in OpenAlex.

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  12. HIV-1 in genital tract and plasma of women: compartmentalization of viral sequences, coreceptor usage, and glycosylation.Proceedings of the National Academy of Sciences of the United States of America · 2003
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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

4 authors at 1 institution in 1 country.

A SinghPulmonary and Critical Care Division, Department of Medicine, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19104-6060, USA.
G Besson
A Mobasher
R G Collman
University of Pennsylvania · US

Funding

HIV ACTIVATION &REGULATION IN LUNG--VIRAL DETERMINANTSR01HL058004 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI COLLMAN, RONALD G · 1996 to 2000
$278k
NHLBI NIH HHS HL 58004
6 · The paper itself

Abstract

Human immunodeficiency virus type 1 (HIV-1) infection is highly compartmentalized, with distinct viral genotypes being found in the lungs, brain, and other organs compared with blood. CCR5 and CXCR4 are the principal HIV-1 coreceptors, and a number of other molecules support entry in vitro but their roles in vivo are uncertain. To address the relationship between tissue compartmentalization and the selective use of entry coreceptors, we generated functional env clones from primary isolates derived from the lungs and blood of three infected individuals and analyzed their use of the principal, secondary, orphan, and virus-encoded coreceptors for fusion. All Env proteins from lung viruses used CCR5 but not CXCR4, while those from blood viruses used CCR5 or CXCR4 or both. The orphan receptor APJ was widely used for fusion by Env proteins from both blood and lung viruses, but none used the cytomegalovirus-encoded receptor US28. Fusion mediated by the secondary coreceptors CCR2b, CCR3, CCR8, and CX3CR1 and orphan receptors GPR1, GPR15, and STRL33 was variable and heterogeneous, with relatively broad utilization by env clones from isolates of one subject but limited use by env clones from the other two subjects. However, there was no clear distinction between blood and lung viruses in secondary or orphan coreceptor fusion patterns. In contrast to fusion, none of the secondary or orphan receptors enabled efficient productive infection. These results confirm, at the level of cofactor utilization, previous observations that HIV-1 populations in the lungs and blood are biologically distinct and demonstrate diversity within lung-derived as well as blood-derived quasispecies. However, the heterogeneity in coreceptor utilization among clones from each isolate and the lack of clear distinction between lung- and blood-derived Env proteins argue against selective coreceptor utilization as a major determinant of compartmentalization.

Indexed as

Receptors, G-Protein-CoupledReceptors, VirusSaccharomyces cerevisiae ProteinsAntigens, CDCell Line, TransformedCloning, MolecularGenes, envGenetic VariationHIV-1HIV SeropositivityHumansLungReceptors, CCR2Receptors, CCR3Receptors, CCR5Receptors, CCR8Antigens, CDCCR2 protein, humanCCR3 protein, humanCCR8 protein, humanCXCR6 protein, humanGPR15 protein, humanGPR1 protein, S cerevisiaeReceptors, CCR2Receptors, CCR3Receptors, CCR5Receptors, CCR8Receptors, Cell SurfaceReceptors, ChemokineReceptors, CXCR4Receptors, CXCR6Receptors, CytokineReceptors, G-Protein-CoupledReceptors, HIVReceptors, InterleukinReceptors, Interleukin-8AReceptors, PeptideReceptors, VirusSaccharomyces cerevisiae Proteins

Identifiers

PMID10400765
PMCPMC112752
OpenAlexW2153292644

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.