Evidence map›Paper›PMID 26078493›Full record

ReviewMediators of inflammation2015

The Role and Potential Therapeutic Application of Myeloid-Derived Suppressor Cells in Allo- and Autoimmunity.

Qi Zhang, Masayuki Fujino, Jinhua Xu, Xiao-kang Li

Abstract readReview
In one paragraph

Review in Mediators of inflammation, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–field-weighted citation impact
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

14 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Adoptive transfer of IFN-γ-induced M-MDSCs promotes immune tolerance to allografts through iNOS pathway.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2019
    Article
  8. Article
  9. Article
  10. CD33Open access Macedonian journal of medical sciences · 2018
    Article
  11. Myeloid-derived suppressor cells in ovarian cancer: friend or foe?Central-European journal of immunology · 2017
    Review
  12. Article
  13. Review
  14. 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

4 authors.

Qi ZhangDepartment of Dermatology, Huashan Hospital, Fudan University, Shanghai, China ; Division of Transplantation Immunology, National Research Institute for Child Health and Development, Tokyo 157-8535, Japan.
Masayuki FujinoDivision of Transplantation Immunology, National Research Institute for Child Health and Development, Tokyo 157-8535, Japan ; AIDS Research Center, National Institute of Infectious Diseases, Tokyo, Japan.
Jinhua XuDepartment of Dermatology, Huashan Hospital, Fudan University, Shanghai, China.
Xiao-kang LiDepartment of Dermatology, Huashan Hospital, Fudan University, Shanghai, China ; Division of Transplantation Immunology, National Research Institute for Child Health and Development, Tokyo 157-8535, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Myeloid-derived suppressor cells (MDSCs) are a heterogeneous population of cells that consists of myeloid progenitor cells and immature myeloid cells. They have been identified as a cell population that may affect the activation of CD4(+) and CD8(+) T-cells to regulate the immune response negatively, which makes them attractive targets for the treatment of transplantation and autoimmune diseases. Several studies have suggested the potential suppressive effect of MDSCs on allo- and autoimmune responses. Conversely, MDSCs have also been found at various stages of differentiation, accumulating during pathological situations, not only during tumor development but also in a variety of inflammatory immune responses, bone marrow transplantation, and some autoimmune diseases. These findings appear to be contradictory. In this review, we summarize the roles of MDSCs in different transplantation and autoimmune diseases models as well as the potential to target these cells for therapeutic benefit.

Indexed as

AnimalsAutoimmunityCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCell DifferentiationHumansMyeloid CellsMyeloid Progenitor Cells

Identifiers

PMID26078493
PMCPMC4452474

What OpenQuestion holds

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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.