Evidence map›Paper›PMID 22228625›Full record

ArticleBlood2012

Emerging roles for multipotent, bone marrow-derived stromal cells in host defense.

Jeffery J Auletta, Robert J Deans, Amelia M Bartholomew

Abstract read
In one paragraph

Article in Blood, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing 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

43 citing papers in PubMed.

  1. Trial
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. [Clinical applications of stem cells from human exfoliated deciduous teeth in stem cell therapy].Hua xi kou qiang yi xue za zhi = Huaxi kouqiang yixue zazhi = West China journal of stomatology · 2017
    Review
  12. Article
  13. [Tumor necrosis factor-α regulates the osteogenic differentiation of bone marrow mesenchymal stem cells in chronic periodontitis].Hua xi kou qiang yi xue za zhi = Huaxi kouqiang yixue zazhi = West China journal of stomatology · 2017
    Article
  14. Article
  15. Article
  16. Guanylate-binding protein 1 (GBP1) contributes to the immunity of human mesenchymal stromal cells against Toxoplasma gondii.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  17. Article
  18. Effectiveness of a novel cellular therapy to treat multidrug-resistant tuberculosis.Journal of clinical tuberculosis and other mycobacterial diseases · 2016
    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

3 authors.

Jeffery J AulettaPediatric Blood and Marrow Transplant Program, Seidman Cancer Center, Cleveland, OH, USA. jeffery.auletta@case.edu
Robert J Deans
Amelia M Bartholomew

Funding

TUMOR METABOLISM PROGRAMP30CA043703 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI MARK R CHANCE · 1987 to 2026
$142.3M
Supercomputing and Multidimensional Data AnalysisP01AI089556 · NIAID · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI SALOMON, DANIEL R. · 2011 to 2015
$11.4M
Distinct functional phases in innate reconstitutionK08AI057801 · NIAID · CASE WESTERN RESERVE UNIVERSITY · PI AULETTA, JEFFERY J · 2004 to 2008
$593k
NCI NIH HHS P30 CA043703NCI NIH HHS P30 CA 43703NIAID NIH HHS AI089556NIAID NIH HHS AI57801NIAID NIH HHS K08 AI057801NIAID NIH HHS P01 AI089556
6 · The paper itself

Abstract

Multipotent, bone marrow-derived stromal cells (BMSCs, also known as mesenchymal stem cells [MSCs]), are culture-expanded, nonhematopoietic cells with immunomodulatory effects currently being investigated as novel cellular therapy to prevent and to treat clinical disease associated with aberrant immune response. Emerging preclinical studies suggest that BMSCs may protect against infectious challenge either by direct effects on the pathogen or through indirect effects on the host. BMSCs may reduce pathogen burden by inhibiting growth through soluble factors or by enhancing immune cell antimicrobial function. In the host, BMSCs may attenuate pro-inflammatory cytokine and chemokine induction, reduce pro-inflammatory cell migration into sites of injury and infection, and induce immunoregulatory soluble and cellular factors to preserve organ function. These preclinical studies provide provocative hints into the direction MSC therapeutics may take in the future. Notably, BMSCs appear to function as a critical fulcrum, providing balance by promoting pathogen clearance during the initial inflammatory response while suppressing inflammation to preserve host integrity and facilitate tissue repair. Such exquisite balance in BMSC function appears intrinsically linked to Toll-like receptor signaling and immune crosstalk.

Indexed as

AnimalsBone Marrow CellsChemokinesCommunicable DiseasesCytokinesHumansImmunomodulationInflammationMesenchymal Stem CellsMiceModels, ImmunologicalMultipotent Stem CellsStromal CellsToll-Like ReceptorsChemokinesCytokinesToll-Like Receptors

Identifiers

PMID22228625
PMCPMC3293637

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.