Evidence map›Paper›PMID 31751473›Full record

ArticleBlood advances2019

Human ectoenzyme-expressing ILC3: immunosuppressive innate cells that are depleted in graft-versus-host disease.

Mette D Hazenberg, Nienke J E Haverkate, Yannouck F van Lier, Hergen Spits, Lisette Krabbendam, Willem A Bemelman, Christianne J Buskens, Bianca Blom, Medya M Shikhagaie

Open access · goldAbstract read
In one paragraph

Article in Blood advances, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

20 citing papers in PubMed, 33 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. ILC3: a case of conflicted identity.Frontiers in immunology · 2023
    Review
  7. Article
  8. Review
  9. Review
  10. Review
  11. Review
  12. Review
  13. Review
  14. EfficientFrontiers in immunology · 2021
    Article
  15. Article
  16. The adenosine pathway in immuno-oncology.Nature reviews. Clinical oncology · 2020
    Review
  17. Review
  18. Review
  19. Innate Lymphocytes in Inflammatory Arthritis.Frontiers in immunology · 2020
    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

9 authors at 2 institutions in 2 countries.

Mette D HazenbergDepartment of Hematology.
Nienke J E HaverkateDepartment of Hematology.
Yannouck F van LierDepartment of Hematology.
Hergen SpitsAmsterdam Infection & Immunity Institute.
Lisette KrabbendamDepartment of Experimental Immunology, and.
Willem A BemelmanDepartment of Gastroenterology, Amsterdam University Medical Center (UMC), location Academic Medical Center (AMC), University of Amsterdam, Amsterdam, The Netherlands.
Christianne J BuskensDepartment of Gastroenterology, Amsterdam University Medical Center (UMC), location Academic Medical Center (AMC), University of Amsterdam, Amsterdam, The Netherlands.
Bianca BlomAmsterdam Infection & Immunity Institute.
Medya M ShikhagaieDepartment of Hematology.
Institute of Infection and Immunity · CAAmsterdam UMC Location University of Amsterdam · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is often associated with chemotherapy- and radiotherapy-induced host tissue damage, leading to graft-versus-host disease (GVHD). Innate lymphoid cells (ILC) have an essential role in tissue homeostasis and tissue repair via their production of interleukin (IL)-22, which acts on intestinal stem cells. The tissue healing capacities of ILC via IL-22 in the context of allo-HSCT and GVHD has previously been demonstrated in a mouse model for acute GVHD. We investigated potential other ways of ILC-mediated tissue protection against GVHD. Tissue injury leads to the release of danger-associated molecular patterns (DAMPs). DAMPs interact with purinergic receptors and ectoenzymes on immune cells and induce pleiotropic effects, including activation of proinflammatory antigen-presenting cells and immunosuppressive effects via the generation of adenosine. Here, we report a novel subset of human ILC3 that coexpress the ectoenzymes CD39 and CD73 (ecto+ ILC3). Ecto+ ILC3 express RORγt and were present in the oral-gastrointestinal tract and bone marrow. ILC3 ectoenzyme expression is modulated by the proinflammatory cytokine IL-1β. Extracellular adenosine triphosphate (eATP) stimulated ecto+ ILC3 to produce IL-22 and adenosine. Activated ecto+ ILC3 suppressed autologous T-cell proliferation in coculture experiments via the production of adenosine. In allo-HSCT recipients, intestinal GVHD was associated with reduced proportions of ecto+ ILC3 and decreased levels of adenosine and its metabolite inosine. Taken together, ecto+ ILC3 have immunosuppressive properties, but in patients with GVHD, ecto+ ILC3 are depleted. A lack of ecto+ ILC3 and subsequent reduced capacity to neutralize DAMPs may contribute to the development of GVHD.

Indexed as

Gene Expression Regulation, EnzymologicImmune ToleranceImmunity, InnateAdenosine TriphosphatasesAdenosine TriphosphateAdultAgedBiomarkersCell ProliferationCytokinesEctopic Gene ExpressionFemaleGraft vs Host DiseaseHematopoietic Stem Cell TransplantationHumansHydrolysisAdenosine TriphosphatasesAdenosine TriphosphateBiomarkersCytokines

Identifiers

PMID31751473
PMCPMC6880892
OpenAlexW2990623561

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.