Evidence map›Paper›PMID 28477096›Full record

ReviewArchivum immunologiae et therapiae experimentalis2017

Expanding Diversity and Common Goal of Regulatory T and B Cells. I: Origin, Phenotype, Mechanisms.

Katarzyna Bocian, Ewelina Kiernozek, Joanna Domagała-Kulawik, Grażyna Korczak-Kowalska, Anna Stelmaszczyk-Emmel, Nadzieja Drela

Erratum issuedAbstract readReview
In one paragraph

Review in Archivum immunologiae et therapiae experimentalis, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Article
  6. Immunobiology of Atherosclerosis: A Complex Net of Interactions.International journal of molecular sciences · 2019
    Review
  7. Review
  8. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Katarzyna BocianDepartment of Immunology, Faculty of Biology, University of Warsaw, Warsaw, Poland. kbocian@biol.uw.edu.pl.
Ewelina KiernozekDepartment of Immunology, Faculty of Biology, University of Warsaw, Warsaw, Poland. ekiernozek@biol.uw.edu.pl.
Joanna Domagała-KulawikDepartment Pneumonology, Medical University of Warsaw, Warsaw, Poland.
Grażyna Korczak-KowalskaDepartment of Immunology, Faculty of Biology, University of Warsaw, Warsaw, Poland.
Anna Stelmaszczyk-EmmelDepartment of Laboratory Diagnostics and Clinical Immunology of Developmental Age, Medical University of Warsaw, Warsaw, Poland.
Nadzieja DrelaDepartment of Immunology, Faculty of Biology, University of Warsaw, Warsaw, Poland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immunosuppressive activity of regulatory T and B cells is critical to limit autoimmunity, excessive inflammation, and pathological immune response to conventional antigens or allergens. Both types of regulatory cells are intensively investigated, however, their development and mechanisms of action are still not completely understood. Both T and B regulatory cells represent highly differentiated populations in terms of phenotypes and origin, however, they use similar mechanisms of action. The most investigated CD4

Indexed as

Immunity, CellularAnimalsBiodiversityB-Lymphocytes, RegulatoryCell DifferentiationCell LineageEpigenesis, GeneticForkhead Transcription FactorsHumansImmunosuppression TherapyPhenotypeReceptors, Antigen, B-CellReceptors, Antigen, T-CellT-Lymphocytes, RegulatoryForkhead Transcription FactorsFOXP3 protein, humanReceptors, Antigen, B-CellReceptors, Antigen, T-CellEpigeneticsImmunosuppressionRegulatory B cellRegulatory T cell

Identifiers

PMID28477096
PMCPMC5688216

What OpenQuestion holds

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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.