Evidence map›Paper›PMID 25880879›Full record

ArticleClinical and experimental immunology2015

Interleukin (IL)-22 receptor 1 is over-expressed in primary Sjogren's syndrome and Sjögren-associated non-Hodgkin lymphomas and is regulated by IL-18.

F Ciccia, G Guggino, A Rizzo, M Bombardieri, S Raimondo, F Carubbi, A Cannizzaro, G Sireci, F Dieli, G Campisi and 5 more

Open access · bronzeAbstract read
In one paragraph

Article in Clinical and experimental immunology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

26 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
  2. The role of IL-22 in cancer.Medical oncology (Northwood, London, England) · 2024
    Review
  3. Article
  4. Review
  5. JAK/STAT Pathway Targeting in Primary Sjögren Syndrome.Rheumatology and immunology research · 2022
    Review
  6. Article
  7. Article
  8. Article
  9. Research progress on inflammatory mechanism of primary Sjögren syndrome.Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences · 2021
    Review
  10. Article
  11. Immunobiology of T Cells in Sjögren's Syndrome.Clinical reviews in allergy & immunology · 2021
    Review
  12. Review
  13. Article
  14. Interleukin-22 Influences the Th1/Th17 Axis.Frontiers in immunology · 2021
    Review
  15. Lymphomagenesis predictors and related pathogenesis.Journal of translational autoimmunity · 2021
    Review
  16. Review
  17. Review
  18. Review
  19. Article
  20. 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

15 authors at 4 institutions in 2 countries.

F CicciaDipartimento Biomedico di Medicina Interna e Specialistica, Sezione di Reumatologia, Palermo, Italy.
G GugginoDipartimento Biomedico di Medicina Interna e Specialistica, Sezione di Reumatologia, Palermo, Italy.
A RizzoAzienda Ospedaliera Ospedali riuniti Villa Sofia-Cervello, Anatomia Patologica, Palermo, Italy.
M BombardieriCentre for Experimental Medicine and Rheumatology, William Harvey Research Institute, Queen Mary University London, UK.
S RaimondoDipartimento di Biopatologia e Biotecnologie Mediche e Forensi, Università di Palermo, Palermo, Italy.
F CarubbiDipartimento di Scienze Cliniche Applicate e Biotecnologiche, Sezione di Reumatologia, Università di L'Aquila, Italy.
A CannizzaroAzienda Ospedaliera Ospedali riuniti Villa Sofia-Cervello, Anatomia Patologica, Palermo, Italy.
G SireciDipartimento di Biopatologia e Biotecnologie Mediche e Forensi, Università di Palermo, Palermo, Italy.
F DieliDipartimento di Biopatologia e Biotecnologie Mediche e Forensi, Università di Palermo, Palermo, Italy.
G CampisiDipartimento di discipline Chirurgiche, Università di Palermo, Italy.
R GiacomelliDipartimento di Scienze Cliniche Applicate e Biotecnologiche, Sezione di Reumatologia, Università di L'Aquila, Italy.
Paola CiprianiDipartimento di Scienze Cliniche Applicate e Biotecnologiche, Sezione di Reumatologia, Università di L'Aquila, Italy.
G De LeoDipartimento di Biopatologia e Biotecnologie Mediche e Forensi, Università di Palermo, Palermo, Italy.
R AlessandroDipartimento di Biopatologia e Biotecnologie Mediche e Forensi, Università di Palermo, Palermo, Italy.
G TrioloDipartimento Biomedico di Medicina Interna e Specialistica, Sezione di Reumatologia, Palermo, Italy.
University of Palermo · ITUniversity of L'Aquila · ITOspedale Vincenzo Cervello · ITWilliam Harvey Research Institute · GB

Funding

Medical Research Council MR/N003063/1
6 · The paper itself

Abstract

The aim of this study was to elucidate more clearly the role of interleukin (IL)-18 in modulating the IL-22 pathway in primary Sjögren's syndrome (pSS) patients and in pSS-associated lymphomas. Minor salivary glands (MSGs) from patients with pSS and non-specific chronic sialoadenitis (nSCS), parotid glands biopsies from non-Hodgkin lymphomas (NHL) developed in pSS patients, were evaluated for IL-18, IL-22, IL-22 receptor 1 (IL-22R1), IL-22 binding protein (IL-22BP) and signal transducer and activator of transcription-3 (STAT-3) expression. MSGs IL-22R1-expressing cells were characterized by confocal microscopy and flow cytometry in pSS, nSCS and healthy controls . The effect of recombinant IL-18 and IL-22 on peripheral blood mononuclear cells (PBMCs) from pSS and nSCS was studied by flow cytometry and reverse transcription-polymerase chain reaction (RT-PCR). MSGs of pSS and NHL were characterized by an imbalance between IL-22 and IL-22BP protein expression, with IL-18 and IL-22BP being expressed in a mutually exclusive manner and IL-18 and IL-22R1 being correlated directly. Aberrant expression of IL-22R1, induced by IL-18, was observed only among tissue and circulating myeloid cells of pSS patients and macrophages of NHL tissues of pSS patients, but not nSCS. IL-22R1 expression on PBMC of pSS was functional, as its stimulation with recombinant IL-22 significantly up-regulated the expression of STAT-3, IL-17 and IL-22. An IL-18-dependent aberrant expression of IL-22R1 on cells of haematopoietic origin seems to be a specific immunological signature of patients with pSS and pSS-associated lymphomas.

Indexed as

AdultAgedFemaleGene Expression RegulationHumansInterleukin-17Interleukin-18Interleukin-22InterleukinsLacrimal ApparatusLeukocytes, MononuclearLymphoma, Non-HodgkinMacrophagesMaleMiddle AgedMyeloid CellsIL22RA2 protein, humanInterleukin-17Interleukin-18Interleukin-22interleukin-22 receptorInterleukinsReceptors, InterleukinSTAT3 protein, humanSTAT3 Transcription FactorIL-18IL-22IL-22BPIL-22R1non-Hodgkin lymphomaSjögren's syndrome

Identifiers

PMID25880879
PMCPMC4516437
OpenAlexW2102942125

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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.