Evidence map›Paper›PMID 17522201›Full record

ArticleJournal of virology2007

CCR5Delta32 protein expression and stability are critical for resistance to human immunodeficiency virus type 1 in vivo.

Lokesh Agrawal, Qingwen Jin, Jeff Altenburg, L Meyer, R Tubiana, Ioannis Theodorou, Ghalib Alkhatib

Open access · greenAbstract read
In one paragraph

Article in Journal of virology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.2field-weighted citation impact, top 25% 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

11 citing papers in PubMed, 22 citations in OpenAlex.

  1. The CD8Microbiology and molecular biology reviews : MMBR · 2021
    Review
  2. Genetically edited CD34Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  3. Review
  4. The technical risks of human gene editing.Human reproduction (Oxford, England) · 2019
    Article
  5. Review
  6. Article
  7. Review
  8. The biology of CCR5 and CXCR4.Current opinion in HIV and AIDS · 2009
    Review
  9. Article
  10. Article
  11. Article
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 6 institutions in 3 countries.

Lokesh AgrawalIndiana University School of Medicine, Department of Microbiology and Immunology, 635 Barnhill Drive, Room 420, Indianapolis, IN 46202, USA.
Qingwen Jin
Jeff Altenburg
L Meyer
R Tubiana
Ioannis Theodorou
Ghalib Alkhatib
Indiana University School of MedicineIndiana University – Purdue University Indianapolis · USNanjing Medical University · CNPitié-Salpêtrière Hospital · FRSorbonne Université · FRUniversité Paris-Sud · FR

Funding

Host Cell Factors and AIDS PathogenesisR01AI052019 · NIAID · TEXAS TECH UNIVERSITY HEALTH SCIS CENTER · PI ALKHATIB, GHALIB ABBAS · 2002 to 2013
$4.0M
NIAID NIH HHS R01 AI052019PHS HHS A152019-01A1
6 · The paper itself

Abstract

Human immunodeficiency virus type 1 (HIV-1) infection of individuals carrying the two alleles of the CCR5Delta32 mutation (CCR5(-/-)) has rarely been reported, but how the virus overcomes the CCR5Delta32 protective effect in these cases has not been delineated. We have investigated this in 6 infected (HIV(+)) and 25 HIV(-) CCR5(-/-) individuals. CD4(+) T lymphocytes isolated from HIV(-) CCR5(-/-) peripheral blood mononuclear cells (PBMCs) showed lower levels of CXCR4 expression that correlated with lower X4 Env-mediated fusion. Endogenous CCR5Delta32 protein was detected in all HIV(-) CCR5(-/-) PBMC samples (n = 25) but not in four of six unrelated HIV(+) CCR5(-/-) PBMC samples. Low levels were detected in another two HIV(+) CCR5(-/-) PBMC samples. The expression of adenovirus 5 (Ad5)-encoded CCR5Delta32 protein restored the protective effect in PBMCs from three HIV(+) CCR5(-/-) individuals but failed to restore the protective effect in PBMCs isolated from another three HIV(+) CCR5(-/-) individuals. In the latter samples, pulse-chase analyses demonstrated the disappearance of endogenous Ad5-encoded CCR5Delta32 protein and the accumulation of Ad5-encoded CCR5 during the chase periods. PBMCs isolated from CCR5(-/-) individuals showed resistance to primary X4 but were readily infected by a lab-adapted X4 strain. Low levels of Ad5-encoded CCR5Delta32 protein conferred resistance to primary X4 but not to lab-adapted X4 virus. These data provide strong support for the hypothesis that the CCR5Delta32 protein actively confers resistance to HIV-1 in vivo and suggest that the loss or reduction of CCR5Delta32 protein expression may account for HIV-1 infection of CCR5(-/-) individuals. The results also suggest that other cellular or virally induced factors may be involved in the stability of CCR5Delta32 protein.

Indexed as

HIV InfectionsAllelesGene Products, envGenotypeHIV-1HumansLeukocytes, MononuclearMutationReceptors, CCR5Receptors, CXCR4Virus InternalizationGene Products, envReceptors, CCR5Receptors, CXCR4

Identifiers

PMID17522201
PMCPMC1951285
OpenAlexW2160704614

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.