Evidence map›Paper›PMID 23630300›Full record

ArticleDiabetes2013

Improvement in β-cell secretory capacity after human islet transplantation according to the CIT07 protocol.

Michael R Rickels, Chengyang Liu, Richard D Shlansky-Goldberg, Scott A Soleimanpour, Kumar Vivek, Malek Kamoun, Zaw Min, Eileen Markmann, Maral Palangian, Cornelia Dalton-Bakes and 5 more

2 registry-linked trialsOpen access · bronzeAbstract read
In one paragraph

Article in Diabetes, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 60 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed, 2 pooled it
11.0field-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.

NCT00434811 phase3completednot on this map

Islet Transplantation in Type 1 Diabetes

TypeinterventionalSponsorNational Institute of Allergy and Infectious Diseases (NIAID)Ran2006 to 2014Enrolled48ConditionsType 1 Diabetes MellitusArmsAllogeneic Pancreatic Islet Cells, Antithymocyte Globulin, Sirolimus, Tacrolimus, Etanercept
NCT01369082 completednot on this map

Extended Follow-Up After Islet Transplantation in Type 1 Diabetes (CIT-08)

TypeobservationalSponsorNational Institute of Allergy and Infectious Diseases (NIAID)Ran2011 to 2017Enrolled75ConditionsType 1 Diabetes (T1D), Islet TransplantationArmsMaintenance Immunosuppressive Treatment
3 · Its place in the literature

Who cites it

60 citing papers in PubMed, 2 syntheses or guidelines pooled it, 102 citations in OpenAlex.

  1. Pooled it
  2. Guideline
  3. Trial
  4. Trial
  5. Successful Application of Closed-Loop Artificial Pancreas Therapy After Islet Autotransplantation.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2016
    Trial
  6. Trial
  7. Trial
  8. Review
  9. Rapid metabolic control after primary islet transplantation: relevance for stem cell-derived islet product development.Transplant international : official journal of the European Society for Organ Transplantation · 2026
    Article
  10. Review
  11. Review
  12. Review
  13. Article
  14. Article
  15. Review
  16. Benefits and Hurdles of Pancreatic β-Cell Replacement.Stem cells translational medicine · 2022
    Review
  17. Article
  18. Observational
  19. Extended survival versus accelerated rejection of nonhuman primate islet allografts: Effect of mesenchymal stem cell source and timing.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2021
    Article
  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

15 authors at 1 institution in 1 country.

Michael R RickelsDivision of Endocrinology, Diabetes, and Metabolism, Department of Medicine, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania, USA. rickels@mail.med.upenn.edu
Chengyang Liu
Richard D Shlansky-Goldberg
Scott A Soleimanpour
Kumar Vivek
Malek Kamoun
Zaw Min
Eileen Markmann
Maral Palangian
Cornelia Dalton-Bakes
Carissa Fuller
Allen J Chiou
Clyde F Barker
Eline T Luning Prak
Ali Naji
University of Pennsylvania · US

Funding

INSTITUTIONAL CLINICAL AND TRANSLATIONAL SCIENCE AWARDUL1RR024134 · NCRR · UNIVERSITY OF PENNSYLVANIA · PI FITZGERALD, GARRET A · 2006 to 2011
$70.4M
Continuation of Clin Islet Transplantation Consortium: Data Coordinating CenterU01DK070431 · NIDDK · UNIVERSITY OF IOWA · PI CLARKE, WILLIAM R. · 2004 to 2014
$54.8M
VIRAL VECTOR COREP30DK019525 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI DOUGLAS J EPSTEIN · 1986 to 2026
$48.3M
Regional Pilot And Feasibility Study Grants ProgramP30DK020572 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Mehboob A Hussain · 2013 to 2026
$24.3M
B-Lymphocyte Immunotherapy in Islet TransplantationU01DK070430 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI NAJI, ALI · 2004 to 2011
$10.1M
Diabetes, Endocrine, and MetabolismT32DK007314 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI DORIS A STOFFERS, Patrick Seale · 1986 to 2026
$9.0M
The Role of Clec16a in the Pancreatic IsletK08DK089117 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI SOLEIMANPOUR, SCOTT · 2012 to 2016
$776k
NCRR NIH HHS UL1 RR024134NIDDK NIH HHS K08 DK089117NIDDK NIH HHS P30 DK019525NIDDK NIH HHS P30 DK020572NIDDK NIH HHS P30 DK19525NIDDK NIH HHS T32 DK007314NIDDK NIH HHS U01 DK070430NIDDK NIH HHS U01DK070430
6 · The paper itself

Abstract

The Clinical Islet Transplantation 07 (CIT07) protocol uses antithymocyte globulin and etanercept induction, islet culture, heparinization, and intensive insulin therapy with the same low-dose tacrolimus and sirolimus maintenance immunosuppression as in the Edmonton protocol. To determine whether CIT07 improves engrafted islet β-cell mass, our center measured β-cell secretory capacity from glucose-potentiated arginine tests at days 75 and 365 after transplantation and compared those results with the results previously achieved by our group using the Edmonton protocol and normal subjects. All subjects were insulin free, with CIT07 subjects receiving fewer islet equivalents from a median of one donor compared with two donors for Edmonton protocol subjects. The acute insulin response to glucose-potentiated arginine (AIRpot) was greater in the CIT07 protocol than in the Edmonton protocol and was less in both cohorts than in normal subjects, with similar findings for C-peptide. The CIT07 subjects who completed reassessment at day 365 exhibited increasing AIRpot by trend relative to that of day 75. These data indicate that engrafted islet β-cell mass is markedly improved with the CIT07 protocol, especially given more frequent use of single islet donors. Although several peritransplant differences may have each contributed to this improvement, the lack of deterioration in β-cell secretory capacity over time in the CIT07 protocol suggests that low-dose tacrolimus and sirolimus are not toxic to islets.

Indexed as

AdultC-PeptideDiabetes Mellitus, Type 1FemaleHumansHypoglycemic AgentsImmunosuppressive AgentsInsulinInsulin-Secreting CellsInsulin SecretionIslets of Langerhans TransplantationMaleMiddle AgedSirolimusTacrolimusTreatment OutcomeC-PeptideHypoglycemic AgentsImmunosuppressive AgentsInsulinSirolimusTacrolimus

Identifiers

PMID23630300
PMCPMC3717864
OpenAlexW2151663279

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

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.