Evidence map›Paper›PMID 19397469›Full record

ArticleTissue engineering. Part A2009

Long-term superior performance of a stem cell/hepatocyte device for the treatment of acute liver failure.

Hiroshi Yagi, Biju Parekkadan, Kazuhiro Suganuma, Alejandro Soto-Gutierrez, Ronald G Tompkins, Arno W Tilles, Martin L Yarmush

Open access · greenAbstract read
In one paragraph

Article in Tissue engineering. Part A, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
3.6field-weighted citation impact, top 7% 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

30 citing papers in PubMed, 63 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Opportunities for biomaterials to address the challenges of COVID-19.Journal of biomedical materials research. Part A · 2020
    Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Effect of bone marrow mesenchymal stem cells on hepatocellular carcinoma in microcirculation.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2013
    Article
  17. Article
  18. Article
  19. Article
  20. Article
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

7 authors at 3 institutions in 2 countries.

Hiroshi YagiCenter for Engineering in Medicine and Surgical Services, Massachusetts General Hospital, Shriners Hospitals for Children and Harvard Medical School, Boston, Massachusetts 02114, USA.
Biju Parekkadan
Kazuhiro Suganuma
Alejandro Soto-Gutierrez
Ronald G Tompkins
Arno W Tilles
Martin L Yarmush
Shriners Hospitals for Children · USShriners Hospitals for Children - Erie · USKeio University · JP

Funding

ROLE OF DIETARY CONSTITUENTS ON GENE EXPRESSION IN INTESTINAL EPITHELIUMP30DK040561 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI Elizabeth Austen Lawson, Takara Leah Stanley · 1994 to 2026
$31.6M
HEPATIC TISSUE ENGINEERINGR01DK043371 · NIDDK · RUTGERS THE ST UNIV OF NJ NEW BRUNSWICK · PI YARMUSH, MARTIN L · 1992 to 2006
$2.4M
Engineering Embryonic Stem Cell Differentiation into HepatocytesK08DK066040 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI TILLES, ARNO W · 2004 to 2008
$566k
NIDDK NIH HHS K08 DK66040NIDDK NIH HHS P30 DK040561NIDDK NIH HHS R01 DK43371
6 · The paper itself

Abstract

Cell-based technologies to support/restore organ function represent one of the most promising avenues in the treatment of acute liver failure (ALF). Recently, mesenchymal stem cells (MSCs) have been reported as a new therapeutic for inflammatory conditions. Here, we demonstrate the efficacy of MSCs, when cocultured with hepatocytes, to provide combination hepatic and antiinflammatory therapy in the setting of ALF. MSCs were shown to have multiple beneficial effects in vitro that were relevant in a therapeutic context, including (1) hepatocellular functional support, (2) secretion of molecules that inhibit hepatocyte apoptosis, and (3) modulation of an acute phase response by hepatocytes cultured in ALF-induced serum. In addition, we show that the MSC secretome is dynamically changed in response to serum exposure from ALF rats. We then conducted a therapeutic trial of liver assist devices (LADs). LADs containing cocultures of MSCs and hepatocytes provided a greater survival benefit compared to other coculture and monocellular control LADs. Treatment with MSC-hepatocyte devices was associated with specific improvements in hepatic functional and histological parameters as well as decreasing inflammatory serum cytokine levels, validating a combined therapeutic effect. Moreover, MSC coculture reduced the overall cell mass of the device by an order of magnitude. These findings demonstrate the importance of nonparenchymal cells in the cellular composition of LADs, and strongly support the integration of MSCs into hepatocyte-coculture-based LADs as a potential destination therapy for ALF.

Indexed as

AnimalsCells, CulturedCoculture TechniquesFemaleHepatocytesLiver Failure, AcuteMesenchymal Stem Cell TransplantationRatsRats, Inbred LewTissue EngineeringTreatment Outcome

Identifiers

PMID19397469
PMCPMC2792056
OpenAlexW1986760247

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.