Evidence map›Paper›PMID 32983164›Full record

ArticleFrontiers in immunology2020

β3-Adrenoceptors as Putative Regulator of Immune Tolerance in Cancer and Pregnancy.

Maura Calvani, Annalisa Dabraio, Angela Subbiani, Daniela Buonvicino, Veronica De Gregorio, Sara Ciullini Mannurita, Alessandro Pini, Patrizia Nardini, Claudio Favre, Luca Filippi

Open access · goldAbstract read
In one paragraph

Article 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 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

21 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. βMedicinal research reviews · 2025
    Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. β-Adrenoceptors in Cancer: Old Players and New Perspectives.Handbook of experimental pharmacology · 2024
    Review
  15. Journal of Cancer · 2024
    Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. 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

10 authors at 2 institutions in 1 country.

Maura CalvaniDepartment of Paediatric Haematology-Oncology, A. Meyer University Children's Hospital, Florence, Italy.
Annalisa DabraioDepartment of Paediatric Haematology-Oncology, A. Meyer University Children's Hospital, Florence, Italy.
Angela SubbianiDepartment of Paediatric Haematology-Oncology, A. Meyer University Children's Hospital, Florence, Italy.
Daniela BuonvicinoDepartment of Health Sciences, University of Florence, Florence, Italy.
Veronica De GregorioDepartment of Paediatric Haematology-Oncology, A. Meyer University Children's Hospital, Florence, Italy.
Sara Ciullini MannuritaDepartment of Paediatric Haematology-Oncology, A. Meyer University Children's Hospital, Florence, Italy.
Alessandro PiniDepartment of Experimental and Clinical Medicine, University of Florence, Florence, Italy.
Patrizia NardiniDepartment of Experimental and Clinical Medicine, University of Florence, Florence, Italy.
Claudio FavreDepartment of Paediatric Haematology-Oncology, A. Meyer University Children's Hospital, Florence, Italy.
Luca FilippiNeonatal Intensive Care Unit, Medical Surgical Feto-Neonatal Department, A. Meyer University Children's Hospital, Florence, Italy.
Meyer Children's Hospital · ITUniversity of Florence · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Understanding the mechanisms of immune tolerance is currently one of the most important challenges of scientific research. Pregnancy affects the immune system balance, leading the host to tolerate embryo alloantigens. Previous reports demonstrated that β-adrenergic receptor (β-AR) signaling promotes immune tolerance by modulation of NK and Treg, mainly through the activation of β2-ARs, but recently we have demonstrated that also β3-ARs induce an immune-tolerant phenotype in mice bearing melanoma. In this report, we demonstrate that β3-ARs support host immune tolerance in the maternal microenvironment by modulating the same immune cells populations as recently demonstrated in cancer. Considering that β3-ARs are modulated by oxygen levels, we hypothesize that hypoxia, through the upregulation of β3-AR, promotes the biological shift toward a tolerant immunophenotype and that this is the same trick that embryo and cancer use to create an aura of immune-tolerance in a competent immune environment. This study confirms the analogies between fetal development and tumor progression and suggests that the expression of β3-ARs represents one of the strategies to induce fetal and tumor immune tolerance.

Indexed as

Models, ImmunologicalAdrenergic beta-3 Receptor AntagonistsAnimalsCell HypoxiaDeciduaFemaleImmune ToleranceImmunocompetenceKiller Cells, NaturalMiceMice, Inbred C57BLNeoplasmsPlacentaPregnancyPregnancy, AnimalPropanolamines3-(2-ethylphenoxy)-1-(1,2,3,4-tetrahydronaphth-1-ylamino)-2-propanol oxalateAdrenergic beta-3 Receptor AntagonistsPropanolaminesReceptors, Adrenergic, beta-3beta-adrenergicbeta-blockerscancer immune-toleranceembryo implantationfetal immune tolerance

Identifiers

PMID32983164
PMCPMC7492666
OpenAlexW3081700680

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.