Evidence map›Paper›PMID 41656162›Full record

ReviewHuman vaccines & immunotherapeutics2026

Harnessing the NKG2D immune surveillance pathway using engineered T-cells for the treatment of human disease.

Maya Glover, John Maher, David Marc Davies

Abstract readReview
In one paragraph

Review in Human vaccines & immunotherapeutics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Review
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

3 authors.

Maya GloverResearch Oncology, Leucid Bio Ltd., Guy's Hospital, London, UK.ORCID 0000-0001-6737-3555
John MaherResearch Oncology, Leucid Bio Ltd., Guy's Hospital, London, UK.
David Marc DaviesResearch Oncology, Leucid Bio Ltd., Guy's Hospital, London, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The NKG2D receptor is a central component of immune surveillance and is expressed on natural killer (NK) cells and several T lymphocyte subsets. NKG2D functions as an activating receptor and costimulatory molecule. By recognizing stress-induced ligands, NKG2D enables immune cells to detect and eliminate virally infected, transformed and senescent cells. Recent advances in engineered T-cell therapies have harnessed this biology through the development of NKG2D-based chimeric antigen receptor (CAR) constructs. Preclinical and early clinical studies demonstrate the versatility of NKG2D-CAR T cells to treat a wide range of human disease types, thereby representing a promising frontier for broad-spectrum immunotherapy of diverse human disease types.

Indexed as

Immunologic SurveillanceImmunotherapyImmunotherapy, AdoptiveNK Cell Lectin-Like Receptor Subfamily KT-LymphocytesAnimalsHumansKiller Cells, NaturalReceptors, Chimeric AntigenKLRK1 protein, humanNK Cell Lectin-Like Receptor Subfamily KReceptors, Chimeric Antigencancer immunotherapychimeric antigen receptor (CAR) T cellsimmune surveillanceimmunotherapyNKG2Dsenescence

Identifiers

PMID41656162
PMCPMC12885400

What Socratic holds

Textmetadata
LicenceCC BY-NC
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 Socratic graph.