Evidence map›Paper›PMID 36560403›Full record

ReviewVaccines2022

Disruption of the NKG2A:HLA-E Immune Checkpoint Axis to Enhance NK Cell Activation against Cancer.

Jack G Fisher, Amber D P Doyle, Lara V Graham, Salim I Khakoo, Matthew D Blunt

Open access · goldAbstract readReview
In one paragraph

Review in Vaccines, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
4.8field-weighted citation impact, top 4% 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

44 citing papers in PubMed, 59 citations in OpenAlex.

  1. Article
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  7. Challenges and opportunities of human iPSC-derived NK as "Off-the-shelf" cellular therapies.Journal of experimental & clinical cancer research : CR · 2025
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  17. Modulation of anti-tumour immunity by XPO1 inhibitors.Exploration of targeted anti-tumor therapy · 2025
    Review
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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

5 authors at 1 institution in 1 country.

Jack G FisherSchool of Clinical and Experimental Sciences, University of Southampton, Southampton SO16 6YD, UK.ORCID 0000-0002-5090-7503
Amber D P DoyleSchool of Clinical and Experimental Sciences, University of Southampton, Southampton SO16 6YD, UK.ORCID 0000-0003-3235-5570
Lara V GrahamSchool of Clinical and Experimental Sciences, University of Southampton, Southampton SO16 6YD, UK.
Salim I KhakooSchool of Clinical and Experimental Sciences, University of Southampton, Southampton SO16 6YD, UK.
Matthew D BluntSchool of Clinical and Experimental Sciences, University of Southampton, Southampton SO16 6YD, UK.ORCID 0000-0003-1099-3985
University of Southampton · GB

Funding

Cancer Research UK 26813Medical Research Council DTP award MR/N014308Medical Research Council MR/M019829/1Medical Research Council MR/S009388/1
6 · The paper itself

Abstract

Ligation of the inhibitory receptor NKG2A by its ligand HLA-E negatively regulates the activation of natural killer (NK) cells, as well as subsets of CD8+ T cells and innate T cell populations. NKG2A has recently become a novel immune checkpoint target for the treatment of cancer and direct antibody mediated blockade of NKG2A function is currently under assessment in two phase 3 clinical trials. In addition to direct targeting, the NKG2A:HLA-E axis can also be disrupted indirectly via multiple different targeted cancer agents that were not previously recognised to possess immunomodulatory properties. Increased understanding of immune cell modulation by targeted cancer therapies will allow for the design of rational and more efficacious drug combination strategies to improve cancer patient outcomes. In this review, we summarise and discuss the various strategies currently in development which either directly or indirectly disrupt the NKG2A:HLA-E interaction to enhance NK cell activation against cancer.

Indexed as

checkpoint blockadeHLA-Eimmunotherapynatural killer cellNK cellNKG2A

Identifiers

PMID36560403
PMCPMC9783329
OpenAlexW4310024016

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.