Evidence map›Paper›PMID 37600026›Full record

ReviewFrontiers in cardiovascular medicine2023

Targeted cell delivery of mesenchymal stem cell therapy for cardiovascular disease applications: a review of preclinical advancements.

Carlos Theodore Huerta, Francesca A Voza, Yulexi Y Ortiz, Zhao-Jun Liu, Omaida C Velazquez

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in cardiovascular medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 10% 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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 9 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Syncytial therapeutics: Receptor-specific and direct-to-cytosol biologic drug delivery mediated by measles fusion complex.Journal of controlled release : official journal of the Controlled Release Society · 2025
    Article
  6. Review
  7. Article
  8. Review
  9. 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

5 authors at 1 institution in 1 country.

Carlos Theodore HuertaDeWitt Daughtry Family Department of Surgery, University of Miami Miller School of Medicine, Miami, FL, United States.
Francesca A VozaDeWitt Daughtry Family Department of Surgery, University of Miami Miller School of Medicine, Miami, FL, United States.
Yulexi Y OrtizDeWitt Daughtry Family Department of Surgery, University of Miami Miller School of Medicine, Miami, FL, United States.
Zhao-Jun LiuDeWitt Daughtry Family Department of Surgery, University of Miami Miller School of Medicine, Miami, FL, United States.
Omaida C VelazquezDeWitt Daughtry Family Department of Surgery, University of Miami Miller School of Medicine, Miami, FL, United States.
University of Miami · US

Funding

Novel Gene Therapy for Critical Limb Ischemia and Limb Salvage in Vascular Occlusive DiseaseR33HL156152 · NHLBI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI LIU, ZHAO-JUN, VELAZQUEZ, OMAIDA C · 2023 to 2024
$1.1M
NHLBI NIH HHS R33 HL156152
6 · The paper itself

Abstract

Cardiovascular diseases (CVD) continue to be the leading cause of morbidity and mortality globally and claim the lives of over 17 million people annually. Current management of CVD includes risk factor modification and preventative strategies including dietary and lifestyle changes, smoking cessation, medical management of hypertension and cholesterol lipid levels, and even surgical revascularization procedures if needed. Although these strategies have shown therapeutic efficacy in reducing major adverse cardiovascular events such as heart attack, stroke, symptoms of chronic limb-threatening ischemia (CLTI), and major limb amputation significant compliance by patients and caregivers is required and off-target effects from systemic medications can still result in organ dysfunction. Stem cell therapy holds major potential for CVD applications but is limited by the low quantities of cells that are able to traffic to and engraft at diseased tissue sites. New preclinical investigations have been undertaken to modify mesenchymal stem cells (MSCs) to achieve targeted cell delivery after systemic administration. Although previous reviews have focused broadly on the modification of MSCs for numerous local or intracoronary administration strategies, here we review recent preclinical advances related to overcoming challenges imposed by the high velocity and dynamic flow of the circulatory system to specifically deliver MSCs to ischemic cardiac and peripheral tissue sites. Many of these technologies can also be applied for the targeted delivery of other types of therapeutic cells for treating various diseases.

Indexed as

cardiovascular diseasecell-based therapychronic limb-threatening ischemiamesenchymal stem cellmyocardial infarctionstem cell therapytargeted cell delivery

Identifiers

PMID37600026
PMCPMC10436297
OpenAlexW4385584013

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.