Evidence map›Paper›PMID 24496181›Full record

ArticleScientific reports2014

Generation and characterization of regulatory dendritic cells derived from murine induced pluripotent stem cells.

Qi Zhang, Masayuki Fujino, Shizue Iwasaki, Hiroshi Hirano, Songjie Cai, Yuya Kitajima, Jinhua Xu, Xiao-Kang Li

Abstract read
In one paragraph

Article in Scientific reports, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Immunoregulatory Cells in Myasthenia Gravis.Frontiers in neurology · 2020
    Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Review
  12. Dendritic cell defects in the colorectal cancer.Human vaccines & immunotherapeutics · 2014
    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

8 authors.

Qi Zhang1] Department of Dermatology, Huashan hospital, Fudan University, Shanghai, China [2] Division of Transplantation Immunology, National Research Institute for Child Health and Development, Tokyo, Japan.
Masayuki Fujino1] Division of Transplantation Immunology, National Research Institute for Child Health and Development, Tokyo, Japan [2] AIDS Research Center, National Institute of Infectious Diseases, Tokyo, Japan.
Shizue IwasakiDivision of Transplantation Immunology, National Research Institute for Child Health and Development, Tokyo, Japan.
Hiroshi Hirano1] Division of Transplantation Immunology, National Research Institute for Child Health and Development, Tokyo, Japan [2] Hasumi International Research Foundation, Tokyo, Japan.
Songjie CaiDivision of Transplantation Immunology, National Research Institute for Child Health and Development, Tokyo, Japan.
Yuya KitajimaDivision of Transplantation Immunology, National Research Institute for Child Health and Development, Tokyo, Japan.
Jinhua XuDepartment of Dermatology, Huashan hospital, Fudan University, Shanghai, China.
Xiao-Kang Li1] Department of Dermatology, Huashan hospital, Fudan University, Shanghai, China [2] Division of Transplantation Immunology, National Research Institute for Child Health and Development, Tokyo, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Regulatory dendritic cells (DCregs) represent a potential therapeutic tool for assessing a variety of immune overreaction conditions; however, current approaches for generating DCregs for therapeutic purposes are limited. We attempted to generate and characterize DCregs from murine induced pluripotent stem (iPS) cells. The iPS cells co-cultured with OP9 cells displayed mesodermally differentiated flat colonies. GM-CSF drove most of the colonies exhibiting a differentiated morphology. Thereafter, cells became morphologically heterologous under the effects of TGF-β and IL-10. Most of the floating cells developed an irregular shape with areas of protrusion. The generated iPS-DCregs demonstrated high CD11b/c and low CD40, CD80, CD86 and MHC-II expressions with a high antigen uptake ability and poor T-cell stimulatory function. Importantly, iPS-DCregs showed immune responsiveness regulation effects both in vitro and in vivo and the ability to generate regulatory T-cells in vitro. Our result illustrates a feasible approach for generating functional DCregs from murine iPS cells.

Indexed as

AnimalsAntigen PresentationB7-1 AntigenB7-2 AntigenCD11b AntigenCD11c AntigenCD40 AntigensCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCell DifferentiationCell LineCell ProliferationDendritic CellsFemaleGranulocyte-Macrophage Colony-Stimulating FactorInduced Pluripotent Stem CellsB7-1 AntigenB7-2 AntigenCD11b AntigenCD11c AntigenCD40 AntigensCd86 protein, mouseGranulocyte-Macrophage Colony-Stimulating FactorIL10 protein, mouseInterleukin-10Transforming Growth Factor beta

Identifiers

PMID24496181
PMCPMC3913921

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Registered trials

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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.