Evidence map›Paper›PMID 35768150›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2022

KIR2DS2 Expression Identifies NK Cells With Enhanced Anticancer Activity.

Matthew D Blunt, Andres Vallejo Pulido, Jack G Fisher, Lara V Graham, Amber D P Doyle, Rebecca Fulton, Matthew J Carter, Marta Polak, Peter W M Johnson, Mark S Cragg and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

9 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Targeting KIR as a novel approach to improve CAR-NK cell function.Journal of translational genetics and genomics · 2023
    Article
  7. Review
  8. Article
  9. 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

12 authors at 1 institution in 1 country.

Matthew D BluntSchool of Clinical and Experimental Sciences, University of Southampton, Southampton, United Kingdom; and m.d.blunt@soton.ac.uk.ORCID 0000-0003-1099-3985
Andres Vallejo PulidoSchool of Clinical and Experimental Sciences, University of Southampton, Southampton, United Kingdom; and.ORCID 0000-0002-4688-0598
Jack G FisherSchool of Clinical and Experimental Sciences, University of Southampton, Southampton, United Kingdom; and.ORCID 0000-0002-5090-7503
Lara V GrahamSchool of Clinical and Experimental Sciences, University of Southampton, Southampton, United Kingdom; and.
Amber D P DoyleSchool of Clinical and Experimental Sciences, University of Southampton, Southampton, United Kingdom; and.ORCID 0000-0003-3235-5570
Rebecca FultonSchool of Clinical and Experimental Sciences, University of Southampton, Southampton, United Kingdom; and.
Matthew J CarterSchool of Cancer Sciences, University of Southampton, Southampton, United Kingdom.
Marta PolakSchool of Clinical and Experimental Sciences, University of Southampton, Southampton, United Kingdom; and.ORCID 0000-0003-2878-476X
Peter W M JohnsonSchool of Cancer Sciences, University of Southampton, Southampton, United Kingdom.ORCID 0000-0003-2306-4974
Mark S CraggSchool of Cancer Sciences, University of Southampton, Southampton, United Kingdom.ORCID 0000-0003-2077-089X
Francesco ForconiSchool of Cancer Sciences, University of Southampton, Southampton, United Kingdom.ORCID 0000-0002-2211-1831
Salim I KhakooSchool of Clinical and Experimental Sciences, University of Southampton, Southampton, United Kingdom; and.
University of Southampton · GB

Funding

Cancer Research UK 23669Cancer Research UK 24721Cancer Research UK 26813Medical Research Council MR/M019829/1Medical Research Council MR/S009388/1
6 · The paper itself

Abstract

NK cells are promising cellular therapeutics against hematological and solid malignancies. Immunogenetic studies have identified that various activating killer cell Ig-like receptors (KIRs) are associated with cancer outcomes. Specifically, KIR2DS2 has been associated with reduced incidence of relapse following transplant in hematological malignancies and improved outcomes in solid tumors, but the mechanism remains obscure. Therefore, we investigated how KIR2DS2 expression impacts NK cell function. Using a novel flow cytometry panel, we show that human NK cells with high KIR2DS2 expression have enhanced spontaneous activation against malignant B cell lines, liver cancer cell lines, and primary chronic lymphocytic leukemia cells. Surface expression of CD16 was increased on KIR2DS2

Indexed as

Killer Cells, NaturalReceptors, KIRAntigens, CD20Cell Line, TumorFlow CytometryHumansRituximabAntigens, CD20KIR2DS2 protein, humanReceptors, KIRRituximab

Identifiers

PMID35768150
PMCPMC7613074
OpenAlexW4283753429

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.