Evidence map›Paper›PMID 30775924›Full record

ArticleNano letters2019

Antibody-Armed Platelets for the Regenerative Targeting of Endogenous Stem Cells.

Deliang Shen, Zhenhua Li, Shiqi Hu, Ke Huang, Teng Su, Hongxia Liang, Feiran Liu, Ke Cheng

Abstract read
In one paragraph

Article in Nano letters, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
4.6field-weighted citation impact, top 5% 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

21 citing papers in PubMed, 43 citations in OpenAlex.

  1. Article
  2. Engineering platelets as cancer therapeutics.Nature reviews. Clinical oncology · 2026
    Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Leukocyte-endothelial interaction in CKD.Clinical kidney journal · 2023
    Review
  11. Article
  12. Article
  13. Review
  14. Review
  15. Review
  16. Review
  17. Article
  18. Review
  19. Utilization of Human Induced Pluripotent Stem Cells for Cardiac Repair.Frontiers in cell and developmental biology · 2020
    Review
  20. 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

8 authors at 1 institution in 2 countries.

Deliang ShenDepartment of Cardiology , The First Affiliated Hospital of Zhengzhou University , Zhengzhou , Henan 450052 , China.
Zhenhua LiDepartment of Molecular Biomedical Sciences and Comparative Medicine Institute , North Carolina State University , Raleigh , North Carolina 27607 , United States.ORCID 0000-0001-9751-0864
Shiqi HuDepartment of Molecular Biomedical Sciences and Comparative Medicine Institute , North Carolina State University , Raleigh , North Carolina 27607 , United States.
Ke HuangDepartment of Molecular Biomedical Sciences and Comparative Medicine Institute , North Carolina State University , Raleigh , North Carolina 27607 , United States.
Teng SuDepartment of Molecular Biomedical Sciences and Comparative Medicine Institute , North Carolina State University , Raleigh , North Carolina 27607 , United States.ORCID 0000-0001-7888-0763
Hongxia LiangDepartment of Cardiology , The First Affiliated Hospital of Zhengzhou University , Zhengzhou , Henan 450052 , China.
Feiran LiuDepartment of Molecular Biomedical Sciences and Comparative Medicine Institute , North Carolina State University , Raleigh , North Carolina 27607 , United States.
Ke ChengDepartment of Cardiology , The First Affiliated Hospital of Zhengzhou University , Zhengzhou , Henan 450052 , China.
University of North Carolina at Chapel Hill · US

Funding

Targeted Nanoparticles for Stem Cell Redirecting and Regenerative MedicineR01HL123920 · NHLBI · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI CHENG, KE · 2015 to 2023
$4.8M
Enhancing vascular delivery of stem cells and microparticlesR01HL137093 · NHLBI · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI CHENG, KE · 2017 to 2020
$1.5M
NHLBI NIH HHS R01 HL123920NHLBI NIH HHS R01 HL137093NIH HHS HL123920NIH HHS HL137093
6 · The paper itself

Abstract

Stem cell therapies have shown promise in treating acute and chronic ischemic heart disease. However, current therapies are limited by the low retention and poor integration of injected cells in the injured tissue. Taking advantage of the natural infarct-homing ability of platelets, we engineered CD34 antibody-linked platelets (P-CD34) to capture circulating CD34-positive endogenous stem cells and direct them to the injured heart. In vitro, P-CD34 could bind to damaged aortas and capture endogenous stem cells in whole blood. In a mouse model of acute myocardial infarction, P-CD34 accumulated in the injured heart after intravenous administration, leading to a concentration of endogenous CD34 stem cells in the injured heart for effective heart repair. This represents a new technology for endogenous stem cell therapy.

Indexed as

Cell- and Tissue-Based TherapyAnimalsAntigens, CD34Blood PlateletsDisease Models, AnimalHeart InjuriesHumansMiceMyocardial InfarctionMyocardiumStem CellsAntigens, CD34antibodiesendogenous stem cellsMyocardium infarctionplatelets

Identifiers

PMID30775924
PMCPMC7025326
OpenAlexW2911931795

What OpenQuestion holds

Textmetadata
LicenceTDM
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.