Evidence map›Paper›PMID 31745336›Full record

ReviewNature immunology2019

Flip the coin: IL-7 and IL-7R in health and disease.

João T Barata, Scott K Durum, Benedict Seddon

Abstract readReview
PubMed Publisher
In one paragraph

Review in Nature immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 249 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
249citing papers in PubMed, 1 pooled it
12.7field-weighted citation impact, top 1% 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

249 citing papers in PubMed, 1 synthesis or guideline pooled it, 378 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Article
  5. Targeting the CD4Molecular biomedicine · 2026
    Article
  6. Key regulatory elements of the TGFβ-LRRC15 axis predict disease progression and immunotherapy resistance across cancer types.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  7. Article
  8. Article
  9. Article
  10. Nodular lymphoid hyperplasia in atypical SCID due to IL7R mutations mimicking CVID.Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology · 2026
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Insulin enables acquisition of the IL7RCell death & disease · 2026
    Article
  17. Article
  18. Article
  19. Article
  20. Article

189 more citing papers are in PubMed but not listed here.

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

3 authors at 3 institutions in 3 countries.

João T BarataInstituto de Medicina Molecular João Lobo Antunes, Faculdade de Medicina, Universidade de Lisboa, Lisbon, Portugal. joao_barata@medicina.ulisboa.pt.ORCID http://orcid.org/0000-0002-4826-8976
Scott K DurumCancer and Inflammation Program, National Cancer Institute, Frederick, MD, USA.
Benedict SeddonInstitute of Immunity and Transplantation, Division of Infection and Immunity, University College London, London, UK.ORCID http://orcid.org/0000-0003-4352-3373
National Cancer Institute · USUniversity College London · GBUniversity of Lisbon · PT

Funding

Medical Research Council MR/P011225/1RCUK | MRC | Medical Research Foundation MR/P011225/1RCUK | MRC | Medical Research Foundation U117573801
6 · The paper itself

Abstract

The cytokine IL-7 and its receptor, IL-7R, are critical for T cell and, in the mouse, B cell development, as well as differentiation and survival of naive T cells, and generation and maintenance of memory T cells. They are also required for innate lymphoid cell (ILC) development and maintenance, and consequently for generation of lymphoid structures and barrier defense. Here we discuss the central role of IL-7 and IL-7R in the lymphoid system and highlight the impact of their deregulation, placing a particular emphasis on their 'dark side' as promoters of cancer development. We also explore therapeutic implications and opportunities associated with either positive or negative modulation of the IL-7-IL-7R signaling axis.

Indexed as

AnimalsCell DifferentiationCell SurvivalHomeostasisHumansImmunotherapyInterleukin-7NeoplasmsReceptors, Interleukin-7T-LymphocytesInterleukin-7Receptors, Interleukin-7

Identifiers

PMID31745336
OpenAlexW2990889969

What OpenQuestion holds

Textmetadata
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.