Evidence map›Paper›PMID 24442207›Full record

ArticleBlood cancer journal2014

Prostaglandin E2 promotes survival of naive UCB T cells via the Wnt/β-catenin pathway and alters immune reconstitution after UCBT.

L Li, H T Kim, A Nellore, N Patsoukis, V Petkova, S McDonough, I Politikos, S Nikiforow, R Soiffer, J H Antin and 4 more

Open access · goldAbstract read
In one paragraph

Article in Blood cancer journal, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

19 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. PGEExperimental hematology · 2017
    Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. How to Improve Cord Blood Engraftment?Frontiers in medicine · 2016
    Review
  17. Suppression of IL-7-dependent Effector T-cell Expansion by Multipotent Adult Progenitor Cells and PGE2.Molecular therapy : the journal of the American Society of Gene Therapy · 2015
    Article
  18. Review
  19. 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

14 authors at 4 institutions in 1 country.

L LiDepartment of Medicine, Division of Hematology/Oncology and Cancer Biology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA.
H T KimDepartment of Biostatistics and Computational Biology, Dana-Farber Cancer Institute, Boston, MA, USA.
A NelloreDepartment of Medicine, Division of Hematology/Oncology and Cancer Biology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA.
N PatsoukisDepartment of Medicine, Division of Hematology/Oncology and Cancer Biology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA.
V PetkovaDepartment of Pathology, Beth Israel Deaconess Medical Center, Boston, MA, USA.
S McDonoughDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
I PolitikosDepartment of Medicine, Division of Hematology/Oncology and Cancer Biology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA.
S NikiforowDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
R SoifferDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
J H AntinDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
K BallenDivision of Hematology/Oncology, Department of Medicine, Massachusetts General Hospital, Boston, MA, USA.
C CutlerDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
J RitzDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
V A BoussiotisDepartment of Medicine, Division of Hematology/Oncology and Cancer Biology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA.
Dana-Farber Cancer Institute · USBeth Israel Deaconess Medical Center · USHarvard University · USMassachusetts General Hospital · US

Funding

Specialized Center for Cell Based TherapyU54HL081030 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI KRONENBERG, HENRY M. · 2005 to 2009
$11.0M
Effects of PGE2 on Reconstitution of Hematopoiesis and Immunity after UCBTR01CA183605 · NCI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI BOUSSIOTIS, VASSILIKI A, CUTLER, COREY S · 2013 to 2017
$3.8M
Manipulation of Immune Responsiveness after Hematopoietic Cell TransplantationR01CA183559 · NCI · DANA-FARBER CANCER INST · PI RITZ, JEROME, SOIFFER, ROBERT JON · 2013 to 2017
$3.7M
Reconstitution of Regulatory T Cells After Stem Cell TransplantationR01CA183560 · NCI · DANA-FARBER CANCER INST · PI RITZ, JEROME, SOIFFER, ROBERT JON · 2013 to 2017
$2.5M
Prevention of acute GvHD by inhibition of cdk2R21HL107997 · NHLBI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI BOUSSIOTIS, VASSILIKI A · 2011 to 2012
$482k
The role of Rap1 and its novel associated molecules in T cell responsesR56AI043552 · NIAID · BETH ISRAEL DEACONESS MEDICAL CENTER · PI BOUSSIOTIS, VASSILIKI A · 2011 to 2011
$392k
NCI NIH HHS R01 CA183559NCI NIH HHS R01 CA183560NCI NIH HHS R01 CA183605NHLBI NIH HHS R21 HL107997NHLBI NIH HHS U54 HL081030NIAID NIH HHS R56 AI043552
6 · The paper itself

Abstract

The outcome of umbilical cord blood transplantation (UCBT) is compromised by low hematopoietic stem cell (HSC) doses leading to prolonged time to engraftment, delayed immunological reconstitution and late memory T-cell skewing. Exposure of UCB to dimethyl-prostaglandin E2 (dmPGE2) increases HSC in vivo. We determined that exposure of UCB T lymphocytes to dmPGE2 modified Wnt signaling resulting in T cell factor (TCF)-mediated transcription. Wnt signaling upregulated interleukin (IL)-7R and IL-2Rβ, resulting in enhanced survival mediated by the homeostatic cytokines IL-7 and IL-15. dmPGE2 also induced components of the Wnt pathway and Wnt receptors, thereby priming UCB T cells to receive signals via Wnt ligands in vivo. We observed that the Wnt transcription factor TCF7 and its target EOMES were elevated in the T cells of patients who received PGE2-treated UCBs. Consistent with the role of Wnt/β-catenin signaling to induce and maintain naive, memory precursors and long-lived central memory CD8(+) cells, these patients also had increased fractions of CD8(+)CD45RO(-)CD62L(+) plus CD8(+)CD45RO(+)CD62L(+) subsets encompassing these T-cell populations. These effects of the PGE2/Wnt/β-catenin axis may have significant implications for harnessing immunity in the context of UCBT, where impaired immune reconstitution is associated with late memory T-cell skewing.

Identifiers

PMID24442207
PMCPMC3913944
OpenAlexW2117348416

What OpenQuestion holds

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LicenceCC BY-NC-SA
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Registered trials

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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.