Evidence map›Paper›PMID 24793563›Full record

ReviewInfection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases2014

CXCR4: a virus's best friend?

Kathleen L Arnolds, Juliet V Spencer

Open access · greenAbstract readReview
In one paragraph

Review in Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

18 citing papers in PubMed, 28 citations in OpenAlex.

  1. mBio · 2025
    Article
  2. Article
  3. Article
  4. CXC chemokine receptor 4 (CXCR4) blockade in cancer treatment.Journal of cancer research and clinical oncology · 2023
    Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Observational
  13. Article
  14. Article
  15. Viral manipulation of the host immune response.Current opinion in immunology · 2015
    Review
  16. Article
  17. Article
  18. 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

2 authors at 1 institution in 1 country.

Kathleen L ArnoldsDepartment of Biology, University of San Francisco, 2130 Fulton Street, San Francisco, CA 94403, United States.
Juliet V SpencerDepartment of Biology, University of San Francisco, 2130 Fulton Street, San Francisco, CA 94403, United States. Electronic address: jspencer@usfca.edu.
University of San Francisco · US

Funding

A Viral Cytokine as a Promoter of Tumor ProgressionR15CA158767 · NCI · UNIVERSITY OF SAN FRANCISCO · PI SPENCER, JULIET VESCIO · 2011 to 2012
$493k
Modification of Host Chemokine Responses by Human CytomegalovirusR15AI111232 · NIAID · UNIVERSITY OF SAN FRANCISCO · PI SPENCER, JULIET VESCIO · 2014 to 2014
$425k
Mechanisms of Cell Signaling by the Human Cytomegalovirus US27 Gene ProductR15AI074029 · NIAID · UNIVERSITY OF SAN FRANCISCO · PI SPENCER, JULIET VESCIO · 2008 to 2008
$212k
NCI NIH HHS R15 CA158767NIAID NIH HHS R15 AI074029NIAID NIH HHS R15 AI111232
6 · The paper itself

Abstract

Viruses are dependent on their hosts for replication and dispersal in the environment; thus, the most successful viruses are those that co-evolve with their hosts. CXCR4 is a cellular chemokine receptor that plays central roles in development, hematopoiesis, and immune surveillance through signaling induced by its ligand, CXCL12. The CXCR4-CXCL12 axis has been besieged by many pathogens that employ a range of strategies to modify or exploit CXCR4 activity. While CXCR4 was identified as a critical co-factor for entry of HIV into CD4+ T cells early on, other viruses may utilize CXCR4 to gain cell entry as well. Moreover, several viruses have been found to modulate CXCR4 expression or alter its functional activity, with direct effects on cell trafficking, immune responses, cell proliferation, and cell survival. Because CXCR4 is targeted by a diverse group of viral pathogens, modification of host CXCR4 signaling activity is emerging as a common theme in virus persistence and is likely to be important for subversion of the host immune system. This review highlights major viral pathogens that use and abuse CXCR4 and explores the possible reasons why this chemokine receptor has become "a virus's best friend".

Indexed as

Cell SurvivalChemokine CXCL12DNA VirusesHost-Pathogen InteractionsHumansReceptors, CXCR4RetroviridaeSignal TransductionChemokine CXCL12Receptors, CXCR4Chemokine receptorCXCL12CXCR4GPCRStromal derived factorTrafficking

Identifiers

PMID24793563
PMCPMC4143154
OpenAlexW2095516781

What OpenQuestion holds

Textmetadata
LicenceTDM
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.