Evidence map›Paper›PMID 40356210›Full record

ArticleArthritis & rheumatology (Hoboken, N.J.)2025

Innate Lymphoid Cell Phenotypic and Functional Alterations in Patients With Systemic Juvenile Idiopathic Arthritis.

Linda Quatrini, Cecilia Ciancaglini, Ivan Caiello, Silvia Santopolo, Manuela Pardeo, Valentina Matteo, Elena Loricchio, Donato Amodio, Elena Morrocchi, Giulio Olivieri and 10 more

Abstract read
In one paragraph

Article in Arthritis & rheumatology (Hoboken, N.J.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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

20 authors.

Linda QuatriniInnate Lymphoid Cells Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.ORCID https://orcid.org/0000-0002-6994-2595
Cecilia CiancagliniTumor Immunology Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Ivan CaielloLaboratory of Immuno-Rheumatology, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Silvia SantopoloInnate Lymphoid Cells Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Manuela PardeoDivision of Rheumatology, ERN RITA Center, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.ORCID https://orcid.org/0000-0003-0850-7351
Valentina MatteoLaboratory of Immuno-Rheumatology, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Elena LoricchioLaboratory of Immuno-Rheumatology, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Donato AmodioClinical and Research Unit of Clinical Immunology and Vaccinology, Bambino Gesù Children's Hospital, IRCCS and Department of Systems Medicine, University of Rome "Tor Vergata," Rome, Italy.
Elena MorrocchiClinical and Research Unit of Clinical Immunology and Vaccinology, Bambino Gesù Children's Hospital, IRCCS and Department of Systems Medicine, University of Rome "Tor Vergata," Rome, Italy.
Giulio OlivieriClinical and Research Unit of Clinical Immunology and Vaccinology, Bambino Gesù Children's Hospital, IRCCS and PhD Program in Immunology, Molecular Medicine and Applied Biotechnology, University of Rome "Tor Vergata," Rome, Italy.
Paolo PalmaClinical and Research Unit of Clinical Immunology and Vaccinology, Bambino Gesù Children's Hospital, IRCCS and Department of Systems Medicine, University of Rome "Tor Vergata," Rome, Italy.
Antonella InsalacoDivision of Rheumatology, ERN RITA Center, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Marco Francesco NataleDivision of Rheumatology, ERN RITA Center, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Arianna De MatteisDivision of Rheumatology, ERN RITA Center, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.ORCID https://orcid.org/0000-0001-6705-4407
Nicola TuminoInnate Lymphoid Cells Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Claudia BracagliaDivision of Rheumatology, ERN RITA Center, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.ORCID https://orcid.org/0000-0002-9834-9619
Paola VaccaInnate Lymphoid Cells Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Lorenzo MorettaTumor Immunology Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Fabrizio De BenedettiLaboratory of Immuno-Rheumatology and Division of Rheumatology, ERN RITA Center, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.ORCID https://orcid.org/0000-0001-8749-8232
Giusi PrencipeLaboratory of Immuno-Rheumatology, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.

Funding

Associazione Italiana per la Ricerca sul Cancro 27022European Union - Next Generation EU - NRRP M6C2 - Investment 2.1 Enhancement and strengthening of biomedical research in the NHS PNRR-MR1-2022-12375873Fondazione Umberto VeronesiMinistero della Salute
6 · The paper itself

Abstract

objectiveSystemic juvenile idiopathic arthritis (sJIA) is a chronic childhood disease classically attributed to innate immune cell dysregulation. This study aimed to elucidate the role of innate lymphoid cells (ILCs), including natural killer (NK) cells and helper-ILCs (hILCs), in sJIA during clinically inactive disease (CID) through phenotypic and functional analysis.

methodsPeripheral ILCs from children with sJIA during CID receiving interleukin-1 (IL-1) inhibitors (n = 40) were analyzed by flow cytometry and compared to 23 healthy children (HC) and 22 patients with unrelated autoinflammatory diseases taking IL-1 inhibitors. Plasma proteomic profiling was also performed.

resultsPatients with sJIA showed a significant reduction in circulating NK cell frequencies compared to HC, with an increased proportion of CD56

conclusionPatients with sJIA in CID exhibit significant innate immune abnormalities, including altered ILC subset distribution and impaired IFNγ production, strongly associated with IL-18 levels. These findings suggest ongoing immune dysregulation despite clinical remission, underscoring a potential role for ILCs and cytokine interaction in sJIA pathogenesis.

Indexed as

Arthritis, JuvenileImmunity, InnateKiller Cells, NaturalLymphocytesAdolescentCase-Control StudiesChildChild, PreschoolFemaleHumansInterferon-gammaInterleukin-1Interleukin-18MalePhenotypeProteomicsInterferon-gammaInterleukin-1Interleukin-18

Identifiers

PMID40356210
PMCPMC12479180

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.