Evidence map›Paper›PMID 28489305›Full record

ArticleAmerican journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons2017

Prolonged Survival Following Pig-to-Primate Liver Xenotransplantation Utilizing Exogenous Coagulation Factors and Costimulation Blockade.

J A Shah, M S Patel, N Elias, N Navarro-Alvarez, I Rosales, R A Wilkinson, N J Louras, M Hertl, J A Fishman, R B Colvin and 4 more

Open access · hybridAbstract read
In one paragraph

Article in American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 65 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
65citing papers in PubMed, 1 pooled it
11.2field-weighted citation impact, top 1% 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

65 citing papers in PubMed, 1 synthesis or guideline pooled it, 121 citations in OpenAlex.

  1. Pooled it
  2. Genetically engineered porcine liver: a new era in transplantation.International journal of surgery (London, England) · 2026
    Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Review
  9. Review
  10. Promise and pitfalls of liver xenotransplantation.Nature reviews. Gastroenterology & hepatology · 2025
    Article
  11. Article
  12. Article
  13. Article
  14. [Research and application progress for liver xenotransplantation].Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2025
    Review
  15. Review
  16. Immunometabolism of Liver Xenotransplantation and Prospective Solutions.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Review
  17. The Future of Pig Liver Xenotransplantation.Transplant international : official journal of the European Society for Organ Transplantation · 2025
    Review
  18. Article
  19. Review
  20. Review

5 more citing papers are in PubMed but not listed here.

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

14 authors at 1 institution in 1 country.

J A ShahCenter for Transplantation Sciences, Massachusetts General Hospital/Harvard Medical School, Boston, MA.ORCID http://orcid.org/0000-0003-2097-0656
M S PatelCenter for Transplantation Sciences, Massachusetts General Hospital/Harvard Medical School, Boston, MA.
N EliasCenter for Transplantation Sciences, Massachusetts General Hospital/Harvard Medical School, Boston, MA.
N Navarro-AlvarezCenter for Transplantation Sciences, Massachusetts General Hospital/Harvard Medical School, Boston, MA.
I RosalesCenter for Transplantation Sciences, Massachusetts General Hospital/Harvard Medical School, Boston, MA.
R A WilkinsonCenter for Transplantation Sciences, Massachusetts General Hospital/Harvard Medical School, Boston, MA.
N J LourasCenter for Transplantation Sciences, Massachusetts General Hospital/Harvard Medical School, Boston, MA.
M HertlCenter for Transplantation Sciences, Massachusetts General Hospital/Harvard Medical School, Boston, MA.
J A FishmanCenter for Transplantation Sciences, Massachusetts General Hospital/Harvard Medical School, Boston, MA.
R B ColvinCenter for Transplantation Sciences, Massachusetts General Hospital/Harvard Medical School, Boston, MA.
A B CosimiCenter for Transplantation Sciences, Massachusetts General Hospital/Harvard Medical School, Boston, MA.
J F MarkmannCenter for Transplantation Sciences, Massachusetts General Hospital/Harvard Medical School, Boston, MA.
D H SachsCenter for Transplantation Sciences, Massachusetts General Hospital/Harvard Medical School, Boston, MA.
P A VagefiCenter for Transplantation Sciences, Massachusetts General Hospital/Harvard Medical School, Boston, MA.
Harvard University · US

Funding

XENOGRAFT TOLERANCE THROUGH MIXED CHIMERISMP01AI045897 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI Megan Sykes · 2000 to 2026
$71.9M
Nonhuman Primate Reagent ResourceU24AI126683 · NIAID · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI Diogo Magnani · 2016 to 2026
$20.1M
TRAINING IN TRANSPLANTATION BIOLOGYT32AI007529 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI MADSEN, JOREN C · 1998 to 2024
$6.4M
NIAID NIH HHS P01 AI045897NIAID NIH HHS T32 AI007529NIAID NIH HHS U24 AI126683
6 · The paper itself

Abstract

Since the first attempt of pig-to-primate liver xenotransplantation (LXT) in 1968, survival has been limited. We evaluated a model utilizing α-1,3-galactosyltransferase knockout donors, continuous posttransplant infusion of human prothrombin concentrate complex, and immunosuppression including anti-thymocyte globulin, FK-506, methylprednisone, and costimulation blockade (belatacept, n = 3 or anti-CD40 mAb, n = 1) to extend survival. Baboon 1 remained well until postoperative day (POD) 25, when euthanasia was required because of cholestasis and plantar ulcers. Baboon 2 was euthanized following a seizure on POD 5, despite normal liver function tests (LFTs) and no apparent pathology. Baboon 3 demonstrated initial stable liver function but was euthanized on POD 8 because of worsening LFTs. Pathology revealed C4d positivity, extensive hemorrhagic necrosis, and a focal cytomegalovirus inclusion. Baboon 4 was clinically well with stable LFTs until POD29, when euthanasia was again necessitated by plantar ulcerations and rising LFTs. Final pathology was C4d negative and without evidence of rejection, inflammation, or thrombotic microangiopathy. Thus, nearly 1-mo rejection-free survival has been achieved following LXT in two of four consecutive recipients, demonstrating that the porcine liver can support life in primates for several weeks and has encouraging potential for clinical application as a bridge to allotransplantation for patients with acute-on-chronic or fulminant hepatic failure.

Indexed as

Transplantation, HeterologousAnimalsAnimals, Genetically ModifiedBlood Coagulation FactorsGraft SurvivalImmunosuppressive AgentsLiver TransplantationPapioSurvival RateSwineBlood Coagulation FactorsImmunosuppressive Agentsbasic (laboratory) research/sciencecoagulation and hemostasisfusion proteins and monoclonal antibodies: costimulation molecule specificgraft survivalimmunosuppressantimmunosuppressive regimensxenotransplantation

Identifiers

PMID28489305
PMCPMC5519420
OpenAlexW2612476374

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.