Evidence map›Paper›PMID 37181001›Full record

ArticleWorld journal of stem cells2023

Repetitive administration of cultured human CD34+ cells improve adenine-induced kidney injury in mice.

Takayasu Ohtake, Shoichi Itaba, Amankeldi A Salybekov, Yin Sheng, Tsutomu Sato, Mitsuru Yanai, Makoto Imagawa, Shigeo Fujii, Hiroki Kumagai, Masamitsu Harata and 2 more

Open access · hybridAbstract read
In one paragraph

Article in World journal of stem cells, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

6 citing papers in PubMed, 6 citations in OpenAlex.

  1. Trial
  2. Development of a potency assay for CD34Scientific reports · 2023
    Trial
  3. Review
  4. Diabetes, Protein Misfolding, and Heat Stress: Molecular Insights and Translational Perspectives.TH open : companion journal to thrombosis and haemostasis · 2026
    Review
  5. Article
  6. Endothelial Progenitor Cells: Disease Markers and Potential Therapy in Kidney Disease.Journal of the American Society of Nephrology : JASN · 2025
    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

12 authors at 1 institution in 1 country.

Takayasu OhtakeRegenerative Medicine, The Center for Cell Therapy & Regenerative Medicine, Shonan Kamakura General Hospital, Kamakura 247-8533, Kanagawa, Japan.
Shoichi ItabaKamakura Techno-science Inc., Kamakura 248-0036, Japan.
Amankeldi A SalybekovRegenerative Medicine, Shonan Research Institute of Innovative Medicine, Kamakura 247-8533, Kanagawa, Japan.
Yin ShengAdvanced Medicine Science, Tokai University School of Medicine, Isehara 259-1193, Japan.
Tsutomu SatoRegenerative Medicine, Shonan Research Institute of Innovative Medicine, Kamakura 247-8533, Kanagawa, Japan.
Mitsuru YanaiDepartment of Pathology, Sapporo Tokushukai Hospital, Sapporo 004-0041, Japan.
Makoto ImagawaDepartment of Pathology, Sapporo Medical Center, Sapporo 004-0041, Japan.
Shigeo FujiiKamakura Techno-science Inc., Kamakura 248-0036, Japan.
Hiroki KumagaiKamakura Techno-science Inc., Kamakura 248-0036, Japan.
Masamitsu HarataHuman Life CORD Japan Inc, Chuo-ku 103-0012, Tokyo, Japan.
Takayuki AsaharaRegenerative Medicine, Shonan Research Institute of Innovative Medicine, Kamakura 247-8533, Kanagawa, Japan.
Shuzo KobayashiRegenerative Medicine, Shonan Research Institute of Innovative Medicine, Kamakura 247-8533, Kanagawa, Japan.
Sapporo Higashi Tokushukai Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThere is no established treatment to impede the progression or restore kidney function in human chronic kidney disease (CKD).

aimTo examine the efficacy of cultured human CD34+ cells with enhanced proliferating potential in kidney injury in mice.

methodsHuman umbilical cord blood (UCB)-derived CD34+ cells were incubated for one week in vasculogenic conditioning medium. Vasculogenic culture significantly increased the number of CD34+ cells and their ability to form endothelial progenitor cell colony-forming units. Adenine-induced tubulointerstitial injury of the kidney was induced in immunodeficient non-obese diabetic/severe combined immunodeficiency mice, and cultured human UCB-CD34+ cells were administered at a dose of 1 × 10

resultsRepetitive administration of cultured UCB-CD34+ cells significantly improved the time-course of kidney dysfunction in the cell therapy group compared with that in the control group. Both interstitial fibrosis and tubular damage were significantly reduced in the cell therapy group compared with those in the control group (

conclusionEarly intervention using human cultured CD34+ cells significantly improved the progression of tubulointerstitial kidney injury. Repetitive administration of cultured human UCB-CD34+ cells significantly improved tubulointerstitial damage in adenine-induced kidney injury in mice

Indexed as

AdenineCD34+ cellChronic kidney diseaseQuality and quantity control cultureTubulointerstitial injuryUmbilical cord blood

Identifiers

PMID37181001
PMCPMC10173816
OpenAlexW4366990599

What Socratic holds

Textmetadata
LicenceCC BY-NC
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 Socratic graph.