Evidence map›Paper›PMID 42099646›Full record

ReviewFrontiers in immunology2026

Physiological, patho-physiological, and potential therapeutic roles for neutrophils in cancer & beyond.

Connor McGarrity-Cottrell, Aoife McGinley, Natalia Becares, Jakub Lich, James Roper, Samuel Florence, Mihil Patel, Mark A Exley

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 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. Leveraging Microphysiological Systems to Facilitate Neutrophil-Based Cancer Immunotherapy.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    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

8 authors.

Connor McGarrity-CottrellLift Biosciences, London Bioscience Innovation Centre, London, United Kingdom.
Aoife McGinleyLift Biosciences, London Bioscience Innovation Centre, London, United Kingdom.
Natalia BecaresLift Biosciences, London Bioscience Innovation Centre, London, United Kingdom.
Jakub LichLift Biosciences, London Bioscience Innovation Centre, London, United Kingdom.
James RoperLift Biosciences, London Bioscience Innovation Centre, London, United Kingdom.
Samuel FlorenceLift Biosciences, London Bioscience Innovation Centre, London, United Kingdom.
Mihil PatelLift Biosciences, London Bioscience Innovation Centre, London, United Kingdom.
Mark A ExleyLift Biosciences, London Bioscience Innovation Centre, London, United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neutrophils are the most common type of white blood cell in the body, acting as crucial mediators of innate immunity. They initiate immune responses against invading microorganisms and threats like cancerous cells. Neutrophil infiltration is observed across inflammatory and autoimmune diseases and many cancers. Neutrophils orchestrate innate and adaptive immune responses to return the body to homeostasis, including after infections and preventing the development of tumours. While both protective and deleterious functions of neutrophils have been reported, this dual functionality reflects the heterogeneity of neutrophil subsets. Previously, neutrophils short lifespan resulted in their underappreciation. Recent advances in technology and methodology have drastically increased understanding of neutrophil biology, heterogeneity and plasticity, leading to a plethora of discoveries around the therapeutic potential of neutrophils, both through their direct cytotoxic effects to remove deleterious populations and through their ability to modulate other components of immunity. How to achieve this therapeutically with a rapidly-turned over population has proven elusive until now. This review highlights physiological and patho-physiological activities of neutrophil populations and their therapeutic potential and challenges. Recent and ongoing efforts to target or exploit neutrophil-type populations therapeutically have included engager-type antibody-based reagents and 'off-the-shelf' allogeneic cell therapy with and 'Immuno-Modulatory Alpha Neutrophils' (IMANs).

Indexed as

NeoplasmsNeutrophilsAnimalsHumansImmunity, InnateImmunotherapyNeutrophil InfiltrationTumor Microenvironmentcancerimmune competenceimmunotherapyneutrophilstumour microenvironment

Identifiers

PMID42099646
PMCPMC13143686

What OpenQuestion holds

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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.