Evidence map›Paper›PMID 36544928›Full record

ArticleLaryngoscope investigative otolaryngology2022

Biobanked tracheal basal cells retain the capacity to differentiate.

Natalie A Kelly, Kimberly M Shontz, Maxwell Bergman, Amy M Manning, Susan D Reynolds, Tendy Chiang

Open access · goldAbstract read
In one paragraph

Article in Laryngoscope investigative otolaryngology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 35% 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

4 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
  2. Tissue-Engineered Tracheal Reconstruction.Biomimetics (Basel, Switzerland) · 2025
    Review
  3. Article
  4. Biobanked tracheal basal cells retain the capacity to differentiate.Laryngoscope investigative otolaryngology · 2022
    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

6 authors at 2 institutions in 1 country.

Natalie A KellyDepartment of Otolaryngology Nationwide Children's Hospital Columbus Ohio USA.ORCID https://orcid.org/0000-0003-4869-4542
Kimberly M ShontzCenter for Regenerative Medicine Abigail Wexner Research Institute at Nationwide Children's Hospital Columbus Ohio USA.
Maxwell BergmanDepartment of Otolaryngology-Head and Neck Surgery The Ohio State Wexner Medical Center Columbus Ohio USA.
Amy M ManningDepartment of Otolaryngology Nationwide Children's Hospital Columbus Ohio USA.
Susan D ReynoldsCenter for Perinatal Medicine Abigail Wexner Research Institute at Nationwide Children's Hospital Columbus Ohio USA.
Tendy ChiangDepartment of Otolaryngology Nationwide Children's Hospital Columbus Ohio USA.ORCID https://orcid.org/0000-0003-1448-5873
Nationwide Children's Hospital · USThe Ohio State University Wexner Medical Center · US

Funding

Tissue-engineered trachea composites for long-segment airway replacement (DIVERSITY SUPP - Hussein)R01HL157039 · NHLBI · RESEARCH INST NATIONWIDE CHILDREN'S HOSP · PI Tendy Chiang · 2021 to 2026
$4.4M
NHLBI NIH HHS R01 HL157039
6 · The paper itself

Abstract

Objective: While airway epithelial biorepositories have established roles in the study of bronchial progenitor stem (basal) cells, the utility of a bank of tracheal basal cells from pediatric patients, who have or are suspected of having an airway disease, has not been established. Methods: Pediatric patients undergoing bronchoscopy were identified and endotracheal brush ( Results: No adverse events were associated with biopsy collection. Of 29 brush biopsies, 16 (55%) were successfully cultured to passage 1/cryopreserved. Samples with higher initial cell yields were more likely to achieve this benchmark. Ten unique donors were then thawed for analysis of differentiation. The average age was 2.2 ± 2.2 years with five donors (50%) having laryngotracheal pathology. Nine donors (90%) demonstrated differentiation capacity at 21 days of culture, as indicated by detection of ciliated cells (ACT+) and mucous cells (MUC5B+). Conclusion: Pediatric tracheal basal cells can be successfully collected and cryopreserved. Recovered cells retain the ability to differentiate into epithelial cell types Level of Evidence: Level 3.

Indexed as

biorepositorypediatricstrachea basal cell collectiontrachea brush biopsy

Identifiers

PMID36544928
PMCPMC9764751
OpenAlexW4306969169

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.