Evidence map›Paper›PMID 20719072›Full record

ArticleCell transplantation2010

Delivery of a therapeutic protein by immune-privileged Sertoli cells.

Katelyn Halley, Emily L Dyson, Gurvinder Kaur, Payal Mital, Peter M Uong, Brinda Dass, Sherry N Crowell, Jannette M Dufour

Open access · greenAbstract read
In one paragraph

Article in Cell transplantation, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
0.7field-weighted citation impact, top 31% 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

20 citing papers in PubMed, 25 citations in OpenAlex.

  1. Testicular immunity.Molecular aspects of medicine · 2024
    Review
  2. Article
  3. Article
  4. Mouse Sertoli Cells Inhibit Humoral-Based Immunity.International journal of molecular sciences · 2022
    Article
  5. Review
  6. Review
  7. Characterization of rodent Sertoli cell primary cultures.Molecular reproduction and development · 2020
    Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. Adult stem cell transplantation: is gender a factor in stemness?International journal of molecular sciences · 2014
    Review
  15. Article
  16. Article
  17. Review
  18. Review
  19. Article
  20. The continued promise of stem cell therapy in regenerative medicine.Medical science monitor : international medical journal of experimental and clinical research · 2011
    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 at 2 institutions in 1 country.

Katelyn HalleyCell Biology and Biochemistry, Texas Tech University Health Sciences Center, Lubbock, TX 79430, USA.
Emily L Dyson
Gurvinder Kaur
Payal Mital
Peter M Uong
Brinda Dass
Sherry N Crowell
Jannette M Dufour
Texas Tech University · USTexas Tech University Health Sciences Center · US

Funding

Transplantation of Genetically Modified, Immune-privileged Steroli CellsR01HD067400 · NICHD · TEXAS TECH UNIVERSITY HEALTH SCIS CENTER · PI DUFOUR, JANNETTE M · 2010 to 2012
$663k
NICHD NIH HHS R01 HD067400
6 · The paper itself

Abstract

Immune-privileged Sertoli cells survive long term after allogeneic or xenogeneic transplantation without the use of immunosuppressive drugs, suggesting they could be used as a vehicle to deliver therapeutic proteins. As a model to test this, we engineered Sertoli cells to transiently produce basal levels of insulin and then examined their ability to lower blood glucose levels after transplantation into diabetic SCID mice. Mouse and porcine Sertoli cells transduced with a recombinant adenoviral vector containing furin-modified human proinsulin cDNA expressed insulin mRNA and secreted insulin protein. Transplantation of 5-20 million insulin-expressing porcine Sertoli cells into diabetic SCID mice significantly decreased blood glucose levels in a dose-dependent manner, with 20 million Sertoli cells decreasing blood glucose levels to 9.8 ± 2.7 mM. Similar results were obtained when 20 million insulin-positive, BALB/c mouse Sertoli cells were transplanted; blood glucose levels dropped to 6.3 ± 2.4 mM and remained significantly lower for 5 days. To our knowledge, this is the first study to demonstrate Sertoli cells can be engineered to produce and secrete a clinically relevant factor that has a therapeutic effect, thus supporting the concept of using immune-privileged Sertoli cells as a potential vehicle for gene therapy.

Indexed as

Drug Delivery SystemsAnimalsBlood GlucoseCells, CulturedDiabetes Mellitus, ExperimentalGenetic TherapyHumansInsulinMaleMiceMice, Inbred BALB CMice, SCIDSertoli CellsSwineBlood GlucoseInsulin

Identifiers

PMID20719072
PMCPMC3087628
OpenAlexW2070426791

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.