Evidence map›Paper›PMID 21491418›Full record

ArticleEuropean journal of immunology2011

A distinct subset of human NK cells expressing HLA-DR expand in response to IL-2 and can aid immune responses to BCG.

J Henry Evans, Amir Horowitz, Maryam Mehrabi, Emma L Wise, James E Pease, Eleanor M Riley, Daniel M Davis

Open access · bronzeAbstract read
In one paragraph

Article in European journal of immunology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

60 citing papers in PubMed, 103 citations in OpenAlex.

  1. Trial
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  5. Review
  6. Review of BCG immunotherapy for bladder cancer.Clinical microbiology reviews · 2025
    Review
  7. Differential impact of TIM-3 ligands on NK cell function.Journal for immunotherapy of cancer · 2025
    Article
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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

7 authors at 3 institutions in 2 countries.

J Henry EvansDivision of Cell and Molecular Biology, Imperial College London, South Kensington Campus, London, UK. evans01@fas.harvard.edu
Amir Horowitz
Maryam Mehrabi
Emma L Wise
James E Pease
Eleanor M Riley
Daniel M Davis
Imperial College London · GBHarvard University · USLondon School of Hygiene & Tropical Medicine · GB

Funding

British Heart Foundation PG/08/031/24823Medical Research Council G0500563Medical Research Council G0900850Medical Research Council G1000758Medical Research Council G1001044Wellcome Trust
6 · The paper itself

Abstract

Subsets of NK cells can have distinct functions. Here, we report that >25% of human peripheral blood NK cells express HLA-DR after culture with IL-2. This can be driven by an expansion of a small subset of NK cells expressing HLA-DR, in contrast to previous assumptions that HLA-DR is upregulated on previously negative cells. HLA-DR-expressing NK cells showed enhanced degranulation to susceptible target cells and expressed chemokine receptor CXCR3, which facilitated their enrichment following exposure to CXCL11/I-TAC. Suggesting HLA-DR-expressing NK cells have an important role in an immune response, stimulation of PBMCs with Mycobacterium bovis BCG (BCG) triggered expansion of this subset. Importantly, the magnitude of an individual's NK cell IFN-γ response triggered by BCG was associated with the initial frequency of HLA-DR-expressing NK cells in PBMCs. More directly indicating the importance of HLA-DR-expressing NK cells, enriching the frequency of this subset in PBMCs substantially augmented the IFN-γ response to BCG. Thus, HLA-DR expression marks a distinct subset of NK cells, present at low frequency in circulating blood but readily expanded by IL-2, that can play an important role during immune responses to BCG.

Indexed as

CD56 AntigenCell CommunicationCell DegranulationChemokine CXCL11Chemotaxis, LeukocyteHLA-DR AntigensHumansInterleukin-2Killer Cells, NaturalLeukocytes, MononuclearLymphocyte ActivationLymphocyte SubsetsMycobacterium bovisReceptors, CXCR3CD56 AntigenChemokine CXCL11CXCL11 protein, humanCXCR3 protein, humanHLA-DR AntigensInterleukin-2Receptors, CXCR3

Identifiers

PMID21491418
PMCPMC3549558
OpenAlexW2152755402

What OpenQuestion holds

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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.