Evidence map›Paper›PMID 23966863›Full record

ArticlePLoS pathogens2013

The viral KSHV chemokine vMIP-II inhibits the migration of Naive and activated human NK cells by antagonizing two distinct chemokine receptors.

Rachel Yamin, Noa S Kaynan, Ariella Glasner, Alon Vitenshtein, Pinchas Tsukerman, Yoav Bauman, Yael Ophir, Shlomo Elias, Yotam Bar-On, Chamutal Gur and 1 more

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

24 citing papers in PubMed, 34 citations in OpenAlex.

  1. Review
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  3. Review
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  6. Review
  7. Review
  8. Review
  9. Review
  10. Article
  11. Kaposi sarcoma.Nature reviews. Disease primers · 2019
    Review
  12. KSHV: Immune Modulation and Immunotherapy.Frontiers in immunology · 2019
    Review
  13. Review
  14. Chemokines encoded by herpesviruses.Journal of leukocyte biology · 2017
    Review
  15. TGF-β1 Downregulates the Expression of CXFrontiers in immunology · 2017
    Article
  16. Review
  17. Review
  18. Viral manipulation of the host immune response.Current opinion in immunology · 2015
    Review
  19. Immune control of oncogenic γ-herpesviruses.Current opinion in virology · 2015
    Review
  20. 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

11 authors at 1 institution in 1 country.

Rachel YaminThe Lautenberg Center for General and Tumor Immunology, The BioMedical Research Institute Israel Canada,Faculty of Medicine (IMRIC), The Hebrew University Hadassah Medical School, Jerusalem, Israel.
Noa S Kaynan
Ariella Glasner
Alon Vitenshtein
Pinchas Tsukerman
Yoav Bauman
Yael Ophir
Shlomo Elias
Yotam Bar-On
Chamutal Gur
Ofer Mandelboim
Hebrew University of Jerusalem · IL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Natural killer (NK) cells are innate immune cells able to rapidly kill virus-infected and tumor cells. Two NK cell populations are found in the blood; the majority (90%) expresses the CD16 receptor and also express the CD56 protein in intermediate levels (CD56(Dim) CD16(Pos)) while the remaining 10% are CD16 negative and express CD56 in high levels (CD56(Bright) CD16(Neg)). NK cells also reside in some tissues and traffic to various infected organs through the usage of different chemokines and chemokine receptors. Kaposi's sarcoma-associated herpesvirus (KSHV) is a human virus that has developed numerous sophisticated and versatile strategies to escape the attack of immune cells such as NK cells. Here, we investigate whether the KSHV derived cytokine (vIL-6) and chemokines (vMIP-I, vMIP-II, vMIP-III) affect NK cell activity. Using transwell migration assays, KSHV infected cells, as well as fusion and recombinant proteins, we show that out of the four cytokine/chemokines encoded by KSHV, vMIP-II is the only one that binds to the majority of NK cells, affecting their migration. We demonstrate that vMIP-II binds to two different receptors, CX3CR1 and CCR5, expressed by naïve CD56(Dim) CD16(Pos) NK cells and activated NK cells, respectively. Furthermore, we show that the binding of vMIP-II to CX3CR1 and CCR5 blocks the binding of the natural ligands of these receptors, Fractalkine (Fck) and RANTES, respectively. Finally, we show that vMIP-II inhibits the migration of naïve and activated NK cells towards Fck and RANTES. Thus, we present here a novel mechanism in which KSHV uses a unique protein that antagonizes the activity of two distinct chemokine receptors to inhibit the migration of naïve and activated NK cells.

Indexed as

CCR5 Receptor AntagonistsAnti-HIV AgentsCell MovementCells, CulturedChemokine CCL5Chemokine CX3CL1ChemokinesCX3C Chemokine Receptor 1CytokinesHerpesvirus 8, HumanHumansImmunoblottingInterleukin-6Killer Cells, NaturalPolymerase Chain ReactionReceptors, CCR5Anti-HIV AgentsCCL5 protein, humanCCR5 protein, humanCCR5 Receptor AntagonistsChemokine CCL5Chemokine CX3CL1ChemokinesCX3C Chemokine Receptor 1CX3CL1 protein, humanCX3CR1 protein, humanCytokinesInterleukin-6Receptors, CCR5Receptors, ChemokinevMIP-II

Identifiers

PMID23966863
PMCPMC3744409
OpenAlexW2106349874

What OpenQuestion holds

Textmetadata
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.