Evidence map›Paper›PMID 31850658›Full record

ArticleAmerican journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons2020

Pancreatic islets engineered with a FasL protein induce systemic tolerance at the induction phase that evolves into long-term graft-localized immune privilege.

Kyle B Woodward, Hong Zhao, Pradeep Shrestha, Lalit Batra, Min Tan, Orlando Grimany-Nuno, Laura Bandura-Morgan, Nadir Askenasy, Haval Shirwan, Esma S Yolcu

Open access · bronzeAbstract 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, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.5field-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

22 citing papers in PubMed, 32 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Engineering hypoimmune stem cell-derived beta cells.Stem cell research & therapy · 2025
    Review
  5. Review
  6. Unlocking Transplant Tolerance with Biomaterials.Advanced healthcare materials · 2025
    Review
  7. Review
  8. Review
  9. Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Engineering pancreatic islets with a novel form of thrombomodulin protein to overcome early graft loss triggered by instant blood-mediated inflammatory reaction.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2023
    Article
  16. Article
  17. Genetic Engineering of Immune Evasive Stem Cell-Derived Islets.Transplant international : official journal of the European Society for Organ Transplantation · 2022
    Review
  18. Review
  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

10 authors at 1 institution in 2 countries.

Kyle B WoodwardDepartment of Microbiology and Immunology, Institute for Cellular Therapeutics, University of Louisville, Louisville, Kentucky.
Hong ZhaoDepartment of Microbiology and Immunology, Institute for Cellular Therapeutics, University of Louisville, Louisville, Kentucky.
Pradeep ShresthaDepartment of Microbiology and Immunology, Institute for Cellular Therapeutics, University of Louisville, Louisville, Kentucky.ORCID 0000-0003-3418-6790
Lalit BatraDepartment of Microbiology and Immunology, Institute for Cellular Therapeutics, University of Louisville, Louisville, Kentucky.ORCID 0000-0002-4375-9004
Min TanDepartment of Microbiology and Immunology, Institute for Cellular Therapeutics, University of Louisville, Louisville, Kentucky.
Orlando Grimany-NunoDepartment of Microbiology and Immunology, Institute for Cellular Therapeutics, University of Louisville, Louisville, Kentucky.
Laura Bandura-MorganDepartment of Microbiology and Immunology, Institute for Cellular Therapeutics, University of Louisville, Louisville, Kentucky.
Nadir AskenasyFrankel Laboratory of Experimental Bone Marrow Transplantation, Petach Tikva, Israel.
Haval ShirwanDepartment of Microbiology and Immunology, Institute for Cellular Therapeutics, University of Louisville, Louisville, Kentucky.ORCID 0000-0002-1657-9470
Esma S YolcuDepartment of Microbiology and Immunology, Institute for Cellular Therapeutics, University of Louisville, Louisville, Kentucky.ORCID 0000-0002-4312-8798
University of Louisville · US

Funding

Training Program in TransplantationT32HL076138 · NHLBI · UNIVERSITY OF LOUISVILLE · PI ILDSTAD, SUZANNE T, SHIRWAN, HAVAL · 2004 to 2013
$2.4M
Targeted delivery of immunomodulatory biologics for induction of immune privilege to allogeneic pancreatic islet graftsU01AI132817 · NIAID · UNIVERSITY OF MISSOURI-COLUMBIA · PI GARCIA, ANDRES J, SHIRWAN, HAVAL · 2017 to 2021
$2.0M
A novel immunomodulatory approach to overcome innate and adaptiveimmune barriers to islet transplantationR01AI121281 · NIAID · UNIVERSITY OF MISSOURI-COLUMBIA · PI SHIRWAN, HAVAL · 2019 to 2024
$1.9M
Engineering pancreatic islets with TGβ protein to overcome rejectionR21AI113348 · NIAID · UNIVERSITY OF LOUISVILLE · PI SHIRWAN, HAVAL · 2015 to 2016
$413k
A novel immunomodulatory approach to overcome innate and adaptive immune barriers to islet transplantationR56AI121281 · NIAID · UNIVERSITY OF LOUISVILLE · PI SHIRWAN, HAVAL · 2016 to 2016
$378k
NHLBI NIH HHS T32 HL076138NIAID NIH HHS R01 AI121281NIAID NIH HHS R21 AI113348NIAID NIH HHS R56 AI121281NIAID NIH HHS U01 AI132817NIH HHS 5T32 HL076138
6 · The paper itself

Abstract

We have previously shown that pancreatic islets engineered to transiently display a modified form of FasL protein (SA-FasL) on their surface survive indefinitely in allogeneic recipients without a need for chronic immunosuppression. Mechanisms that confer long-term protection to allograft are yet to be elucidated. We herein demonstrated that immune protection evolves in two distinct phases; induction and maintenance. SA-FasL-engineered allogeneic islets survived indefinitely and conferred protection to a second set of donor-matched, but not third-party, unmanipulated islet grafts simultaneously transplanted under the contralateral kidney capsule. Protection at the induction phase involved a reduction in the frequency of proliferating alloreactive T cells in the graft-draining lymph nodes, and required phagocytes and TGF-β. At the maintenance phase, immune protection evolved into graft site-restricted immune privilege as the destruction of long-surviving SA-FasL-islet grafts by streptozotocin followed by the transplantation of a second set of unmanipulated islet grafts into the same site from the donor, but not third party, resulted in indefinite survival. The induced immune privilege required both CD4

Indexed as

Islets of LangerhansIslets of Langerhans TransplantationFas Ligand ProteinGraft SurvivalImmune PrivilegeImmune ToleranceFas Ligand Proteinbasic (laboratory) research/sciencecell death: apoptosisgraft survivalislet transplantationtolerancetranslational research/science

Identifiers

PMID31850658
PMCPMC7299172
OpenAlexW2995235591

What OpenQuestion holds

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Registered trials

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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.