Evidence map›Paper›PMID 26853275›Full record

ReviewNature reviews. Nephrology2016

Mesenchymal stromal cells in renal transplantation: opportunities and challenges.

Federica Casiraghi, Norberto Perico, Monica Cortinovis, Giuseppe Remuzzi

Abstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Nephrology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 72 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
72citing papers in PubMed, 1 pooled it
13.7field-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

72 citing papers in PubMed, 1 synthesis or guideline pooled it, 170 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Trial
  5. Allogeneic Mesenchymal Stem Cells for Treatment of AKI after Cardiac Surgery.Journal of the American Society of Nephrology : JASN · 2018
    Trial
  6. Cellular and Molecular Aspects of Chronic Rejection.Results and problems in cell differentiation · 2026
    Review
  7. Review
  8. Review
  9. Review
  10. Article
  11. Review
  12. Review
  13. Frontiers in aging · 2023
    Article
  14. Review
  15. Organ Repair and Regeneration DuringTransplant international : official journal of the European Society for Organ Transplantation · 2023
    Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article

12 more citing papers are in PubMed but not listed here.

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

4 authors at 2 institutions in 1 country.

Federica CasiraghiIRCCS - Istituto di Ricerche Farmacologiche Mario Negri, Transplant Research Center "Chiara Cucchi de Alessandri e Gilberto Crespi", Via G.B. Camozzi 3, 24020 Ranica, Bergamo, Italy.
Norberto PericoIRCCS - Istituto di Ricerche Farmacologiche Mario Negri, Clinical Research Center for Rare Diseases "Aldo &Cele Daccò", Via G.B. Camozzi 3, 24020 Ranica, Bergamo, Italy.
Monica CortinovisIRCCS - Istituto di Ricerche Farmacologiche Mario Negri, Transplant Research Center "Chiara Cucchi de Alessandri e Gilberto Crespi", Via G.B. Camozzi 3, 24020 Ranica, Bergamo, Italy.
Giuseppe RemuzziIRCCS - Istituto di Ricerche Farmacologiche Mario Negri, Clinical Research Center for Rare Diseases "Aldo &Cele Daccò", Via G.B. Camozzi 3, 24020 Ranica, Bergamo, Italy.
Mario Negri Institute for Pharmacological Research · ITIstituti di Ricovero e Cura a Carattere Scientifico · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lifelong immunosuppressive therapy is essential to prevent allograft rejection in transplant recipients. Long-term, nonspecific immunosuppression can, however, result in life-threatening complications and fail to prevent chronic graft rejection. Bone marrow (BM)-derived multipotent mesenchymal stromal cells (MSCs) have emerged as a potential candidate for cell-based therapy to modulate the immune response in organ transplantation. These cells can repair tissue after injury and downregulate many of the effector functions of immune cells that participate in the alloimmune response, converting them into regulatory cells. The findings of preclinical and initial clinical studies support the potential tolerance-inducing effects of MSCs and highlight the unanticipated complexity of MSC therapy in kidney transplantation. In animal models of transplantation MSCs promote donor-specific tolerance through the generation of regulatory T cells and antigen-presenting cells. In some settings, however, MSCs can acquire proinflammatory properties and contribute to allograft dysfunction. The available data from small clinical studies suggest that cell infusion is safe and well tolerated by kidney transplant recipients. Ongoing and future trials will provide evidence regarding the long-term safety of MSC therapy and determine the optimum cell source (either autologous or allogeneic) and infusion protocol to achieve operational tolerance in kidney transplant recipients. These studies will also provide additional evidence regarding the risks and benefits of MSC infusion and will hopefully offer definitive answers to the important questions of when, where, how many and which types of MSCs should be infused to fully exploit their immunomodulatory, pro-tolerogenic and tissue-repairing properties.

Indexed as

AnimalsAntigen-Presenting CellsGraft RejectionHumansImmunosuppressive AgentsKidney Failure, ChronicKidney TransplantationMesenchymal Stem CellsMesenchymal Stem Cell TransplantationT-Lymphocytes, RegulatoryTransplantation, HomologousTransplantation ToleranceImmunosuppressive Agents

Identifiers

PMID26853275
OpenAlexW2268790843

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.