Evidence map›Paper›PMID 41906686›Full record

ArticleClinical and experimental immunology2026

Altered neutrophil signalling linked to impaired chemotaxis and increased ROS and NET production in older people with frailty.

Genna Ali Abdullah, Jack Walsh, Andrew Sellin, Cody McLean, Asangaedem Akpan, Marie M Phelan, Helen L Wright

Abstract read
In one paragraph

Article in Clinical and experimental immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Genna Ali AbdullahInstitute of Life Course and Medical Sciences, University of Liverpool, Liverpool, UK.
Jack WalshInstitute of Systems, Molecular and Integrative Biology, University of Liverpool, Liverpool, UK.
Andrew SellinInstitute of Life Course and Medical Sciences, University of Liverpool, Liverpool, UK.
Cody McLeanSchool of Biosciences, University of Liverpool, Liverpool, UK.
Asangaedem AkpanBunbury Regional Hospital, Bunbury, Western Australia, Australia.
Marie M PhelanInstitute of Systems, Molecular and Integrative Biology, University of Liverpool, Liverpool, UK.
Helen L WrightInstitute of Life Course and Medical Sciences, University of Liverpool, Liverpool, UK.ORCID 0000-0003-0442-3134

Funding

University of LiverpoolUniversity of Liverpool BiosciencesVivensa Foundation
6 · The paper itself

Abstract

Immune function alters with age, and is often accompanied by low-grade inflammation (inflammageing). In individuals with frailty, inflammageing is increased, dysregulating immune function and increasing susceptibility to serious outcomes from infection. In this study, we investigated the changes that take place in human neutrophils during healthy ageing and ageing with frailty (FR) using RNAseq and functional assays. We also compared neutrophil phenotype in frailty with rheumatoid arthritis (RA). RNAseq data were analysed using IDEP2 and Ingenuity Pathway Analysis (IPA). Neutrophil phenotype was assessed for reactive oxygen species (ROS) production, neutrophil extracellular trap (NET) release, chemotaxis, and bacterial killing capacity. Experimental data were analysed by ANOVA in R (v4.5.1). RNAseq identified activation of G-protein coupled receptors, interferon and cytokine receptor signalling, and chemotaxis pathways in frail individuals (n = 10) compared with healthy older (n = 9) and healthy younger people (n = 8, adj. P < 0.05). FR neutrophils expressed more IL-8 receptors (CXCR1 and CXCR2) and CD177 on their surface (n = 5-8, P < 0.05). FR and RA neutrophils released significantly more ROS (n = 6-7) and had impaired chemotaxis (n = 8-9) and bacterial killing capacity (n = 5, P < 0.05) compared with both healthy groups. FR neutrophils also released significantly more NETs in response to LPS (10 ng/ml, n = 6-7, P < 0.05). This work provides novel insight into the altered neutrophil phenotype associated with ageing in good health and ageing with frailty, and highlights similarities between inflammageing in frailty and chronic inflammation in RA. This may be important in the development of therapeutics and/or health management strategies to support healthy living as we age.

Indexed as

AgingChemotaxisExtracellular TrapsFrailtyNeutrophilsReactive Oxygen SpeciesAdultAgedAged, 80 and overArthritis, RheumatoidFemaleHumansMaleMiddle AgedReceptors, Interleukin-8AReceptors, Interleukin-8BReactive Oxygen SpeciesReceptors, Interleukin-8AReceptors, Interleukin-8BchemotaxisNETsneutrophilsignallingtranscriptomics

Identifiers

PMID41906686
PMCPMC13089575

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Registered trials

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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.