Evidence map›Paper›PMID 33329534›Full record

ReviewFrontiers in immunology2020

Anti-Tumorigenic Activities of IL-33: A Mechanistic Insight.

Sara Andreone, Adriana Rosa Gambardella, Jacopo Mancini, Stefania Loffredo, Simone Marcella, Valentina La Sorsa, Gilda Varricchi, Giovanna Schiavoni, Fabrizio Mattei

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 14% 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

29 citing papers in PubMed, 1 synthesis or guideline pooled it, 40 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. IL-33 and IL-33-derived DC-based tumor immunotherapy.Experimental & molecular medicine · 2024
    Review
  10. Review
  11. Article
  12. International journal of molecular sciences · 2024
    Article
  13. Article
  14. Review
  15. Discovery of highly immunogenic spleen-resident FCGR3Cellular & molecular immunology · 2023
    Article
  16. Review
  17. Article
  18. The role of IL-33/ST2 signaling in the tumor microenvironment and Treg immunotherapy.Experimental biology and medicine (Maywood, N.J.) · 2022
    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

9 authors at 3 institutions in 1 country.

Sara AndreoneDepartment of Oncology and Molecular Medicine, Istituto Superiore di Sanità, Rome, Italy.
Adriana Rosa GambardellaDepartment of Oncology and Molecular Medicine, Istituto Superiore di Sanità, Rome, Italy.
Jacopo ManciniDepartment of Oncology and Molecular Medicine, Istituto Superiore di Sanità, Rome, Italy.
Stefania LoffredoDepartment of Translational Medical Sciences and Center for Basic and Clinical Immunology Research (CISI), University of Naples Federico II, Naples, Italy.
Simone MarcellaDepartment of Translational Medical Sciences and Center for Basic and Clinical Immunology Research (CISI), University of Naples Federico II, Naples, Italy.
Valentina La SorsaResearch Coordination and Support Service, CoRI, Istituto Superiore di Sanità, Rome, Italy.
Gilda VarricchiDepartment of Translational Medical Sciences and Center for Basic and Clinical Immunology Research (CISI), University of Naples Federico II, Naples, Italy.
Giovanna SchiavoniDepartment of Oncology and Molecular Medicine, Istituto Superiore di Sanità, Rome, Italy.
Fabrizio MatteiDepartment of Oncology and Molecular Medicine, Istituto Superiore di Sanità, Rome, Italy.
Istituto Superiore di Sanità · ITUniversity of Naples Federico II · ITNational Research Council · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Interleukin-33 (IL-33) is an epithelial-derived cytokine that can be released upon tissue damage, stress, or infection, acting as an alarmin for the immune system. IL-33 has long been studied in the context of Th2-related immunopathologies, such as allergic diseases and parasitic infections. However, its capacity to stimulate also Th1-type of immune responses is now well established. IL-33 binds to its specific receptor ST2 expressed by most immune cell populations, modulating a variety of responses. In cancer immunity, IL-33 can display both pro-tumoral and anti-tumoral functions, depending on the specific microenvironment. Recent findings indicate that IL-33 can effectively stimulate immune effector cells (NK and CD8

Indexed as

AnimalsCarcinogenesisCD8-Positive T-LymphocytesEosinophilsHumansImmunity, InnateImmunotherapyInterleukin-1 Receptor-Like 1 ProteinInterleukin-33Killer Cells, NaturalNeoplasmsSignal TransductionTumor MicroenvironmentIL1RL1 protein, humanInterleukin-1 Receptor-Like 1 ProteinInterleukin-33basophilsCD8 T cellseosinophilsIL-33ILC2immune checkpointstumor immunitytumor microenvironment

Identifiers

PMID33329534
PMCPMC7734277
OpenAlexW3107862853

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.