Evidence map›Paper›PMID 25783967›Full record

ReviewMucosal immunology2015

In situ hematopoiesis: a regulator of TH2 cytokine-mediated immunity and inflammation at mucosal surfaces.

C C K Hui, K M McNagny, J A Denburg, M C Siracusa

Open access · bronzeAbstract readReview
PubMed Publisher
In one paragraph

Review in Mucosal immunology, 2015. 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
1.9field-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

20 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Immune responses and exacerbations in severe asthma.Current opinion in immunology · 2021
    Review
  5. Review
  6. Article
  7. Review
  8. Article
  9. Review
  10. House Dust Mite Induces Bone Marrow IL-33-Responsive ILC2s and TInternational journal of molecular sciences · 2020
    Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. Frontiers in pediatrics · 2018
    Article
  17. Mepolizumab Attenuates Airway Eosinophil Numbers, but Not Their Functional Phenotype, in Asthma.American journal of respiratory and critical care medicine · 2017
    Article
  18. Article
  19. Article
  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

4 authors at 2 institutions in 1 country.

C C K HuiDivision of Clinical Immunology and Allergy, Department of Medicine, McMaster University, Hamilton, Ontario, Canada.
K M McNagnyBiomedical Research Center, University of British Columbia, Vancouver, British Columbia, Canada.
J A DenburgDivision of Clinical Immunology and Allergy, Department of Medicine, McMaster University, Hamilton, Ontario, Canada.
M C SiracusaCenter for Immunity and Inflammation, Department of Medicine, New Jersey Medical School, Rutgers-The State University of New Jersey, Newark, New Jersey, USA.
McMaster University · CAUniversity of British Columbia · CA

Funding

Interrogating innate immunity to helminth parasitesK22AI110573 · NIAID · RBHS-NEW JERSEY MEDICAL SCHOOL · PI SIRACUSA, MARK CHRISTOPHER · 2015 to 2016
$270k
Canadian Institutes of Health Research MOP-111029Canadian Institutes of Health Research MOP-133589NIAID NIH HHS 1K22AI110573
6 · The paper itself

Abstract

Hematopoiesis refers to the development of blood cells in the body through the differentiation of pluripotent stem cells. Although hematopoiesis is a multifocal process during embryonic development, under homeostatic conditions it occurs exclusively within the bone marrow. There, a limited number of hematopoietic stem cells differentiate into a rapidly proliferating population of lineage-restricted progenitors that serve to replenish circulating blood cells. However, emerging reports now suggest that under inflammatory conditions, alterations in hematopoiesis that occur outside of the bone marrow appear to constitute a conserved mechanism of innate immunity. Moreover, recent reports have identified previously unappreciated pathways that regulate the egress of hematopoietic progenitor cells from the bone marrow, alter their activation status, and skew their developmental potential. These studies suggest that progenitor cells contribute to inflammatory response by undergoing in situ hematopoiesis (ISH). In this review, we highlight the differences between homeostatic hematopoiesis, which occurs in the bone marrow, and ISH, which occurs at mucosal surfaces. Further, we highlight factors produced at local sites of inflammation that regulate hematopoietic progenitor cell responses and the development of TH2 cytokine-mediated inflammation. Finally, we discuss the therapeutic potential of targeting ISH in preventing the development of inflammation at mucosal sites.

Indexed as

ImmunityAnimalsCytokinesEpithelial CellsHelminthsHematopoiesisHematopoietic Stem CellsHumansHypersensitivityInflammationIntercellular Signaling Peptides and ProteinsLymphocyte SubsetsMucous MembraneTh2 CellsCytokinesIntercellular Signaling Peptides and Proteins

Identifiers

PMID25783967
OpenAlexW2038478436

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.