Evidence map›Paper›PMID 31742878›Full record

ArticleLiver transplantation : official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society2020

Autologous Adipose Tissue-Derived Mesenchymal Stem Cells Introduced by Biliary Stents or Local Immersion in Porcine Bile Duct Anastomoses.

Yi Zhang, Ayushman Sharma, Dong Jin Joo, Erek Nelson, Anan AbuRmilah, Bruce P Amiot, Christen J Boyer, Jonathan S Alexander, Nidhi Jalan-Sakrikar, John Martin and 7 more

Open access · greenAbstract read
In one paragraph

Article in Liver transplantation : official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

6 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. [Review of Research Progress in Biliary Substitutes].Sichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition · 2021
    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

17 authors at 2 institutions in 3 countries.

Yi ZhangDepartment of Surgery, Mayo Clinic and Foundation, Rochester, MN.
Ayushman SharmaDepartment of Surgery, Mayo Clinic and Foundation, Rochester, MN.
Dong Jin JooDepartment of Surgery, Mayo Clinic and Foundation, Rochester, MN.
Erek NelsonDepartment of Surgery, Mayo Clinic and Foundation, Rochester, MN.
Anan AbuRmilahDepartment of Surgery, Mayo Clinic and Foundation, Rochester, MN.ORCID 0000-0002-6743-8280
Bruce P AmiotDepartment of Surgery, Mayo Clinic and Foundation, Rochester, MN.
Christen J BoyerDepartment of Molecular and Cellular Physiology, Louisiana State University Health Sciences Center, Shreveport, LA.
Jonathan S AlexanderDepartment of Molecular and Cellular Physiology, Louisiana State University Health Sciences Center, Shreveport, LA.
Nidhi Jalan-SakrikarGastroenterology Research Unit, Mayo Clinic and Foundation, Rochester, MN.
John MartinDivision of Gastroenterology and Hepatology, Mayo Clinic and Foundation, Rochester, MN.
Roger MoreiraDepartment of Laboratory Medicine and Pathology, Mayo Clinic and Foundation, Rochester, MN.
Shiraj A ChowdhuryGastroenterology Research Unit, Mayo Clinic and Foundation, Rochester, MN.
Michele SmartDepartment of Laboratory Medicine and Pathology, Mayo Clinic and Foundation, Rochester, MN.
Allan B DietzDepartment of Laboratory Medicine and Pathology, Mayo Clinic and Foundation, Rochester, MN.
Scott L NybergDepartment of Surgery, Mayo Clinic and Foundation, Rochester, MN.
Julie K HeimbachDepartment of Surgery, Mayo Clinic and Foundation, Rochester, MN.
Robert C HuebertGastroenterology Research Unit, Mayo Clinic and Foundation, Rochester, MN.ORCID 0000-0002-9812-7573
Mayo Clinic · USLouisiana State University Health Sciences Center Shreveport · US

Funding

PILOT AND FEASIBILTY PROGRAMP30DK084567 · NIDDK · MAYO CLINIC ROCHESTER · PI Samar Ibrahim · 2009 to 2026
$22.2M
Molecular Mechanisms of Cholestatic FibrogenesisR01DK117861 · NIDDK · MAYO CLINIC ROCHESTER · PI Robert Christian Huebert · 2019 to 2026
$2.8M
Immunodeficient FAH-/- PigsR01DK106667 · NIDDK · MAYO CLINIC ROCHESTER · PI NYBERG, SCOTT L · 2015 to 2019
$2.1M
Epigenetic Regulation in Primary Sclerosing CholangitisR03DK113339 · NIDDK · MAYO CLINIC ROCHESTER · PI HUEBERT, ROBERT CHRISTIAN · 2018 to 2019
$159k
NIDDK NIH HHS P30 DK084567NIDDK NIH HHS R01 DK106667NIDDK NIH HHS R01 DK117861NIDDK NIH HHS R03 DK113339
6 · The paper itself

Abstract

Biliary complications (strictures and leaks) represent major limitations in living donor liver transplantation. Mesenchymal stem cells (MSCs) are a promising modality to prevent biliary complications because of immunosuppressive and angiogenic properties. Our goal was to evaluate the safety of adipose-derived MSC delivery to biliary anastomoses in a porcine model. Secondary objectives were defining the optimal method of delivery (intraluminal versus extraluminal) and to investigate MSC engraftment, angiogenesis, and fibrosis. Pigs were divided into 3 groups. Animals underwent adipose collection, MSC isolation, and expansion. Two weeks later, animals underwent bile duct transection, reanastomosis, and stent insertion. Group 1 received plastic stents wrapped in unseeded Vicryl mesh. Group 2 received stents wrapped in MSC-seeded mesh. Group 3 received unwrapped stents with the anastomosis immersed in an MSC suspension. Animals were killed 1 month after stent insertion when cholangiograms and biliary tissue were obtained. Serum was collected for liver biochemistries. Tissue was used for hematoxylin-eosin and trichrome staining and immunohistochemistry for MSC markers (CD44 and CD34) and for a marker of neoangiogenesis (CD31). There were no intraoperative complications. One pig died on postoperative day 3 due to acute cholangitis. All others recovered without complications. Cholangiography demonstrated no biliary leaks and minimal luminal narrowing. Surviving animals exhibited no symptoms, abnormal liver biochemistries, or clinically significant biliary stricturing. Group 3 showed significantly greater CD44 and CD34 staining, indicating MSC engraftment. Fibrosis was reduced at the anastomotic site in group 3 based on trichrome stain. CD31 staining of group 3 was more pronounced, supporting enhanced neoangiogenesis. In conclusion, adipose-derived MSCs were safely applied to biliary anastomoses. MSCs were locally engrafted within the bile duct and may have beneficial effects in terms of fibrosis and angiogenesis.

Indexed as

Liver TransplantationMesenchymal Stem CellsAnimalsBile DuctsHumansImmersionLiving DonorsPostoperative ComplicationsStentsSwine

Identifiers

PMID31742878
PMCPMC7061488
OpenAlexW2991644914

What OpenQuestion holds

Textmetadata
LicenceTDM
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.