Evidence map›Paper›PMID 29078330›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2017

Favorable outcome of experimental islet xenotransplantation without immunosuppression in a nonhuman primate model of diabetes.

Barbara Ludwig, Stefan Ludwig, Anja Steffen, Yvonne Knauf, Baruch Zimerman, Sophie Heinke, Susann Lehmann, Undine Schubert, Janine Schmid, Martina Bleyer and 13 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
11.4field-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

39 citing papers in PubMed, 119 citations in OpenAlex.

  1. Review
  2. Review
  3. GHRH in diabetes and metabolism.Reviews in endocrine & metabolic disorders · 2025
    Review
  4. Cell Therapy for T1D Beyond BLA: Gearing Up Toward Clinical Practice.Diabetes therapy : research, treatment and education of diabetes and related disorders · 2025
    Review
  5. Contributions of Europeans to Xenotransplantation Research: 2. Pig Islet and Cell Xenotransplantation.Transplant international : official journal of the European Society for Organ Transplantation · 2025
    Review
  6. Review
  7. Review
  8. Review
  9. Double transgenic neonatal porcine islets as an alternative source for beta cell replacement therapy.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  10. Article
  11. Review
  12. Review
  13. Review
  14. Enhanced Insulin Production From Porcine Islets: More Insulin, Less Islets.Transplant international : official journal of the European Society for Organ Transplantation · 2024
    Review
  15. Review
  16. A wireless, battery-free device enables oxygen generation and immune protection of therapeutic xenotransplants in vivo.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  17. Article
  18. Article
  19. Article
  20. Preferred Islet Delivery Device Characteristics and Implantation Strategies of Patients With Type 1 Diabetes.Transplant international : official journal of the European Society for Organ Transplantation · 2023
    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

23 authors at 9 institutions in 4 countries.

Barbara LudwigDepartment of Medicine III, University Hospital Carl Gustav Carus, Dresden D-01307, Germany; Barbara.Ludwig@uniklinikum-dresden.de andrew.schally@va.gov.
Stefan LudwigDepartment of Surgery, University Hospital Carl Gustav Carus, Dresden D-01307, Germany.
Anja SteffenDepartment of Medicine III, University Hospital Carl Gustav Carus, Dresden D-01307, Germany.
Yvonne KnaufPathology Unit, German Primate Center, Leibniz-Institute for Primate Research, Göttingen D-37077, Germany.
Baruch ZimermanBeta-O2 Technologies, Petach-Tikva 49511, Israel.
Sophie HeinkeDepartment of Pediatrics, University Hospital Carl Gustav Carus, Dresden D-01307, Germany.
Susann LehmannDepartment of Medicine III, University Hospital Carl Gustav Carus, Dresden D-01307, Germany.
Undine SchubertDepartment of Medicine III, University Hospital Carl Gustav Carus, Dresden D-01307, Germany.
Janine SchmidDepartment of Medicine III, University Hospital Carl Gustav Carus, Dresden D-01307, Germany.
Martina BleyerPathology Unit, German Primate Center, Leibniz-Institute for Primate Research, Göttingen D-37077, Germany.
Uwe SchönmannPathology Unit, German Primate Center, Leibniz-Institute for Primate Research, Göttingen D-37077, Germany.
Clark K ColtonDepartment of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139.
Ezio BonifacioDFG-Center for Regenerative Therapies Dresden, Technische Universität Dresden D-01307, Germany.
Michele SolimenaPaul Langerhans Institute Dresden of the Helmholtz Center Munich at The University Hospital Carl Gustav Carus and Faculty of Medicine of the TU Dresden, Dresden D-01307, Germany.
Andreas ReichelDepartment of Medicine III, University Hospital Carl Gustav Carus, Dresden D-01307, Germany.
Andrew V SchallyDepartment of Pathology, Miller School of Medicine, University of Miami, Miami, FL 33136; Barbara.Ludwig@uniklinikum-dresden.de andrew.schally@va.gov.
Avi RotemBeta-O2 Technologies, Petach-Tikva 49511, Israel.
Uriel BarkaiBeta-O2 Technologies, Petach-Tikva 49511, Israel.
Helena Grinberg-RashiBeta-O2 Technologies, Petach-Tikva 49511, Israel.
Franz-Josef KaupPathology Unit, German Primate Center, Leibniz-Institute for Primate Research, Göttingen D-37077, Germany.
Yuval AvniBeta-O2 Technologies, Petach-Tikva 49511, Israel.
Peter JonesDivision of Diabetes & Nutritional Sciences, Faculty of Life Sciences & Medicine, King's College London, London SE1 1UL, United Kingdom.
Stefan R BornsteinDepartment of Medicine III, University Hospital Carl Gustav Carus, Dresden D-01307, Germany.
University Hospital Carl Gustav Carus · DEBeta-O2 Technologies (Israel) · ILGerman Primate Center · DEPaul Langerhans Institute Dresden · DEGerman Center for Diabetes Research · DEKing's College London · GBMassachusetts Institute of Technology · USTechnische Universität Dresden · DEUniversity of Miami · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Transplantation of pancreatic islets for treating type 1 diabetes is restricted to patients with critical metabolic lability resulting from the need for immunosuppression and the shortage of donor organs. To overcome these barriers, we developed a strategy to macroencapsulate islets from different sources that allow their survival and function without immunosuppression. Here we report successful and safe transplantation of porcine islets with a bioartificial pancreas device in diabetic primates without any immune suppression. This strategy should lead to pioneering clinical trials with xenotransplantation for treatment of diabetes and, thereby, represents a previously unidentified approach to efficient cell replacement for a broad spectrum of endocrine disorders and other organ dysfunctions.

Indexed as

AnimalsDiabetes Mellitus, ExperimentalDiabetes Mellitus, Type 1FemaleImmunosuppression TherapyIslets of LangerhansIslets of Langerhans TransplantationPrimatesSwineTransplantation, Heterologousbeta-cell replacementdiabetesimmune barrierporcine islets

Identifiers

PMID29078330
PMCPMC5676906
OpenAlexW2765726679

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.