Evidence map›Paper›PMID 41805640›Full record

ArticleThe Journal of clinical investigation2026

Graft-derived VWF drives platelet activation and thrombocytopenia during porcine liver xenotransplantation to brain-dead human recipients.

Liang Zhao, Sokratis A Apostolidis, Aae Suzuki, Amrita Sarkar, Qian Guo, Felix Li, Alex Sagar, John Fallon, Mohamed A Elzawahry, Syed Hussain Abbas and 10 more

Abstract read
In one paragraph

Article in The Journal of clinical investigation, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

20 authors.

Liang ZhaoDepartment of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Sokratis A ApostolidisDepartment of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Aae SuzukiDepartment of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Amrita SarkarChildren's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
Qian GuoDivision of Transplantation, Department of Surgery, New York University Langone Health, New York, New York, USA.
Felix LiDepartment of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Alex SagarNuffield Department of Surgical Sciences, University of Oxford, The Churchill Hospital, Oxford, United Kingdom.
John FallonNuffield Department of Surgical Sciences, University of Oxford, The Churchill Hospital, Oxford, United Kingdom.
Mohamed A ElzawahryNuffield Department of Surgical Sciences, University of Oxford, The Churchill Hospital, Oxford, United Kingdom.
Syed Hussain AbbasNuffield Department of Surgical Sciences, University of Oxford, The Churchill Hospital, Oxford, United Kingdom.
Leanne LanierieGenesis, Cambridge, Massachusetts, USA.
Kristen GetchelleGenesis, Cambridge, Massachusetts, USA.
Susan C LoweGenesis, Cambridge, Massachusetts, USA.
Kim M OlthoffPenn Transplant Institute, Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Emma E FurthDepartment of Pathology and Laboratory Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Brendan J KeatingDivision of Transplantation, Department of Surgery, New York University Langone Health, New York, New York, USA.
Peter FriendNuffield Department of Surgical Sciences, University of Oxford, The Churchill Hospital, Oxford, United Kingdom.
Mortimer PonczChildren's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
Abraham ShakedPenn Transplant Institute, Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Charles S AbramsDepartment of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.

Funding

Studies of Physiologic and Pathologic Platelet Plug FormationP01HL146373 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI PONCZ, MORTIMER · 2020 to 2024
$12.2M
New Mechanistic Insights & Therapeutic Applications of Megakaryocytes/PlateletsR35HL150698 · NHLBI · CHILDREN'S HOSP OF PHILADELPHIA · PI Mortimer Poncz · 2020 to 2026
$7.3M
Immunobiology and Physiology of Liver xenograft in the DecedentU01AI191397 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI abraham na shaked · 2025 to 2026
$2.6M
The Novel Mechanisms of Thrombosis Formation in Myeloproliferative DiseasesR01HL148014 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI ABRAMS, CHARLES S. · 2020 to 2023
$2.5M
Single-cell dissection of CD4 T cell changes in patients with immune-related adverse events following PD-1 inhibitionK08AR081929 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI Sokratis Apostolidis · 2023 to 2026
$691k
NHLBI NIH HHS P01 HL146373NHLBI NIH HHS R01 HL148014NHLBI NIH HHS R35 HL150698NIAID NIH HHS U01 AI191397NIAMS NIH HHS K08 AR081929
6 · The paper itself

Abstract

BACKGROUNDGenetically engineered porcine livers are being developed as a bridge therapy for acute liver failure, providing detoxification and restoration of hepatic protein synthesis. Severe xenograft-associated thrombocytopenia remains a major limitation, and human mechanistic data are scarce.METHODSPlatelet kinetics were characterized in 3 human decedents undergoing extracorporeal cross-circulation with transgenic porcine livers. Platelet counts, transfusion requirements, and clearance patterns were assessed to distinguish consumption from marrow suppression or hypersplenism. Antibody- and complement-directed inhibitors were administered to test immune-mediated mechanisms. Mechanistic studies focused on porcine von Willebrand factor-dependent (pVWF-dependent) platelet activation, including ex vivo blockade with the anti-VWF nanobody caplacizumab, a VWF-directed antibody fragment that prevents VWF-platelet binding. A fourth decedent received caplacizumab during porcine liver perfusion.RESULTSIn all 3 initial cases, 80%-90% of circulating and transfused platelets were rapidly cleared, a pattern inconsistent with marrow suppression or hypersplenism. Antibody and complement inhibition failed to ameliorate thrombocytopenia. Recipient plasma induced robust pVWF-mediated platelet activation analogous to human type IIb von Willebrand disease, which was completely abrogated ex vivo by caplacizumab. In a fourth decedent treated with caplacizumab, aberrant platelet activation was prevented, although full hematologic recovery was limited by preexisting disseminated intravascular coagulation.CONCLUSIONSEarly thrombocytopenia during porcine liver xenotransplantation appears to be primarily driven by pVWF-mediated platelet activation rather than by classical immune or splenic mechanisms. Targeted VWF blockade with agents such as caplacizumab may mitigate platelet loss and improve the safety profile of extracorporeal porcine liver support in acute liver failure.

Indexed as

Liver TransplantationPlatelet ActivationThrombocytopeniaTransplantation, Heterologousvon Willebrand FactorAnimalsAnimals, Genetically ModifiedBlood PlateletsFemaleHeterograftsHumansMaleMiddle AgedSwinevon Willebrand FactorHematologyTransplantationVascular biology

Identifiers

PMID41805640
PMCPMC13132372

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.