Evidence map›Paper›PMID 16341058›Full record

ArticleGene therapy2006

Inhibition of CD26 peptidase activity significantly improves engraftment of retrovirally transduced hematopoietic progenitors.

C Tian, J Bagley, D Forman, J Iacomini

Abstract read
PubMed Publisher
In one paragraph

Article in Gene therapy, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

15 citing papers in PubMed, 35 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Umbilical cord transplantation: epilogue.Seminars in hematology · 2010
    Review
  12. Experimental basis of cord blood transplantation.Bone marrow transplantation · 2009
    Review
  13. Review
  14. Article
  15. 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

4 authors at 2 institutions in 1 country.

C TianTransplantation Research Center, Brigham and Women's Hospital and Children's Hospital Boston, Harvard Medical School, Boston, MA 02115, USA.
J Bagley
D Forman
J Iacomini
Brigham and Women's Hospital · USHarvard University · US

Funding

TRAINING IN TRANSPLANTATION BIOLOGYT32AI007529 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI MADSEN, JOREN C · 1998 to 2024
$6.4M
TOLERANCE TO ALLOGRAFTS THROUGH GENE THERAPYR01AI043619 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI IACOMINI, JOHN J · 1998 to 2008
$2.4M
Preventing Xenograft Rejection by Molecular ChimerismR01AI050602 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI IACOMINI, JOHN J · 2003 to 2005
$1.4M
NIAID NIH HHS R01AI43619-06NIAID NIH HHS R01AI50602-02NIAID NIH HHS T32 AI07529
6 · The paper itself

Abstract

It has previously been shown that inhibition of CD26 (DPPIV/dipeptidylpeptidase IV) peptidase activity improves homing of hematopoietic stem cells (HSCs) to the bone marrow and increases engraftment efficiency. Here, we demonstrate that treatment of retrovirally transduced mouse bone marrow cells with the tri-peptide Diprotin A (Ile-Pro-Ile), a specific inhibitor of CD26, significantly enhances engraftment of retrovirally transduced HSCs. Treatment of transduced bone marrow cells with Diprotin A permitted long-term expression of a retrovirally encoded MHC class I gene on multiple hematopoietic cell lineages after transplantation of a suboptimal number of transduced cells. Secondary transfer experiments revealed that expression of the transduced MHC class I gene resulted from engraftment of transduced HSCs. Expression of the allogeneic MHC class I antigen on bone marrow-derived cells following transplantation of Diprotin A-treated cells was sufficient to induce transplantation tolerance. Therefore, inhibition of CD26 activity significantly enhances engraftment of limited numbers of genetically modified HSCs, resulting in physiologically relevant levels of gene transfer.

Indexed as

Genes, MHC Class IHematopoietic Stem Cell TransplantationAnimalsDipeptidyl Peptidase 4Gene ExpressionGenetic TherapyGenetic VectorsGraft SurvivalHematopoietic Stem CellsImmune ToleranceMiceOligopeptidesRadiation ChimeraRetroviridaeTransduction, GeneticTransplantation ImmunologyDipeptidyl Peptidase 4diprotin AOligopeptides

Identifiers

PMID16341058
OpenAlexW2035838146

What OpenQuestion holds

Textmetadata
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.