Evidence map›Paper›PMID 29971065›Full record

ArticleFrontiers in immunology2018

Prostaglandin E2 Stimulates the Expansion of Regulatory Hematopoietic Stem and Progenitor Cells in Type 1 Diabetes.

Moufida Ben Nasr, Francesca D'Addio, Amir Mohammad Malvandi, Silvia Faravelli, Eduardo Castillo-Leon, Vera Usuelli, Francesca Rocchio, Teresa Letizia, Abdel Basset El Essawy, Emma Assi and 13 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

13 citing papers in PubMed, 16 citations in OpenAlex.

  1. Review
  2. Review
  3. Harnessing prostaglandin ETrends in immunology · 2023
    Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Hematopoietic Stem Cells in Type 1 Diabetes.Frontiers in immunology · 2021
    Review
  10. Review
  11. Review
  12. Article
  13. 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 6 institutions in 3 countries.

Moufida Ben NasrNephrology Division, Boston Children's Hospital, Harvard Medical School, Boston, MA, United States.
Francesca D'AddioInternational Center for T1D, Pediatric Clinical Research Center Fondazione Romeo ed Enrica Invernizzi, Department of Biomedical and Clinical Science L. Sacco, University of Milan, Milan, Italy.
Amir Mohammad MalvandiInternational Center for T1D, Pediatric Clinical Research Center Fondazione Romeo ed Enrica Invernizzi, Department of Biomedical and Clinical Science L. Sacco, University of Milan, Milan, Italy.
Silvia FaravelliInternational Center for T1D, Pediatric Clinical Research Center Fondazione Romeo ed Enrica Invernizzi, Department of Biomedical and Clinical Science L. Sacco, University of Milan, Milan, Italy.
Eduardo Castillo-LeonNephrology Division, Boston Children's Hospital, Harvard Medical School, Boston, MA, United States.
Vera UsuelliNephrology Division, Boston Children's Hospital, Harvard Medical School, Boston, MA, United States.
Francesca RocchioInternational Center for T1D, Pediatric Clinical Research Center Fondazione Romeo ed Enrica Invernizzi, Department of Biomedical and Clinical Science L. Sacco, University of Milan, Milan, Italy.
Teresa LetiziaInternational Center for T1D, Pediatric Clinical Research Center Fondazione Romeo ed Enrica Invernizzi, Department of Biomedical and Clinical Science L. Sacco, University of Milan, Milan, Italy.
Abdel Basset El EssawyMedicine, Al-Azhar University, Cairo, Egypt.
Emma AssiInternational Center for T1D, Pediatric Clinical Research Center Fondazione Romeo ed Enrica Invernizzi, Department of Biomedical and Clinical Science L. Sacco, University of Milan, Milan, Italy.
Chiara MameliDepartment of Pediatrics, Buzzi Children Hospital, Milan, Italy.
Elisa GianiDepartment of Pediatrics, Buzzi Children Hospital, Milan, Italy.
Maddalena MacedoniDepartment of Pediatrics, Diabetes Service Studies, University of Milan, Ospedale dei Bambini Vittore Buzzi, Milan, Italy.
Anna MaestroniInternational Center for T1D, Pediatric Clinical Research Center Fondazione Romeo ed Enrica Invernizzi, Department of Biomedical and Clinical Science L. Sacco, University of Milan, Milan, Italy.
Alice DassanoInternational Center for T1D, Pediatric Clinical Research Center Fondazione Romeo ed Enrica Invernizzi, Department of Biomedical and Clinical Science L. Sacco, University of Milan, Milan, Italy.
Cristian LoretelliInternational Center for T1D, Pediatric Clinical Research Center Fondazione Romeo ed Enrica Invernizzi, Department of Biomedical and Clinical Science L. Sacco, University of Milan, Milan, Italy.
Moira ParoniDepartment of Bioscience, University of Milan, Milan, Italy.
Giuseppe CannalireDepartment of Pediatrics and Neonatology, Ospedale Guglielmo da Saliceto, Piacenza, Italy.
Giacomo BiasucciDepartment of Pediatrics and Neonatology, Ospedale Guglielmo da Saliceto, Piacenza, Italy.
Marco SalaDepartment of Pediatrics, Tradate Hospital, Tradate, Italy.
Alessandra BiffiGene Therapy Program, Dana-Farber/Boston Children's Cancer and Blood Disorders Center, Boston, MA, United States.
Gian Vincenzo ZuccottiInternational Center for T1D, Pediatric Clinical Research Center Fondazione Romeo ed Enrica Invernizzi, Department of Biomedical and Clinical Science L. Sacco, University of Milan, Milan, Italy.
Paolo FiorinaNephrology Division, Boston Children's Hospital, Harvard Medical School, Boston, MA, United States.
University of Milan · ITHarvard University · USGuglielmo da Saliceto Hospital · ITAl-Azhar University · EGFoundation Jewish Contemporary Documentation Center · ITOspedale dei Bambini Vittore Buzzi · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hematopoietic stem and progenitor cells (HSPCs) are multipotent stem cells that have been harnessed as a curative therapy for patients with hematological malignancies. Notably, the discovery that HSPCs are endowed with immunoregulatory properties suggests that HSPC-based therapeutic approaches may be used to treat autoimmune diseases. Indeed, infusion with HSPCs has shown promising results in the treatment of type 1 diabetes (T1D) and remains the only "experimental therapy" that has achieved a satisfactory rate of remission (nearly 60%) in T1D. Patients with newly diagnosed T1D have been successfully reverted to normoglycemia by administration of autologous HSPCs in association with a non-myeloablative immunosuppressive regimen. However, this approach is hampered by a high incidence of adverse effects linked to immunosuppression. Herein, we report that while the use of autologous HSPCs is capable of improving C-peptide production in patients with T1D,

Indexed as

autoimmune diseasesCXCR4hematopoietic stem and progenitor cellsPD-L1prostaglandins

Identifiers

PMID29971065
PMCPMC6018202
OpenAlexW2805324180

What OpenQuestion 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 OpenQuestion graph.