Evidence map›Paper›PMID 26227158›Full record

ReviewStem cells (Dayton, Ohio)2015

In Vitro T-Cell Generation From Adult, Embryonic, and Induced Pluripotent Stem Cells: Many Roads to One Destination.

Michelle J Smith, Beau R Webber, Mahmood Mohtashami, Heather E Stefanski, Juan Carlos Zúñiga-Pflücker, Bruce R Blazar

Abstract readReview
In one paragraph

Review in Stem cells (Dayton, Ohio), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
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

10 citing papers in PubMed.

  1. Generation ofHeliyon · 2024
    Article
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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.

Michelle J SmithDivision of Pediatric Blood and Marrow Transplant, University of Minnesota, Minneapolis, Minnesota, USA.
Beau R WebberDivision of Pediatric Blood and Marrow Transplant, University of Minnesota, Minneapolis, Minnesota, USA.
Mahmood MohtashamiDepartment of Immunology, University of Toronto, Sunnybrook Research Institute, Toronto, Ontario, Canada.
Heather E StefanskiDivision of Pediatric Blood and Marrow Transplant, University of Minnesota, Minneapolis, Minnesota, USA.
Juan Carlos Zúñiga-PflückerDepartment of Immunology, University of Toronto, Sunnybrook Research Institute, Toronto, Ontario, Canada.
Bruce R BlazarDivision of Pediatric Blood and Marrow Transplant, University of Minnesota, Minneapolis, Minnesota, USA.

Funding

Women's CancerP30CA077598 · NCI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI Douglas Yee · 1998 to 2026
$100.4M
Trial Design and Biostatistical Support CoreP01CA065493 · NCI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI Mark J Osborn · 1995 to 2026
$48.2M
TRAINING IN HEMOGLOBIN &CELL MEMBRANE RESEARCHT32HL007062 · NHLBI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI Jeffrey S. Miller, Gregory M Vercellotti · 1985 to 2026
$10.3M
GVL TO REDUCE AML RELAPSE AFTER MURINE ALLOGENEIC BMTR01CA072669 · NCI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI BLAZAR, BRUCE R · 1997 to 2017
$4.9M
COMPUTERIZED SYMPTOM REPORT CONSULT FOR CANCER PATIENTSR01CA081918 · NCI · UNIVERSITY OF WASHINGTON · PI WILKIE, DIANA J · 1999 to 2006
$3.9M
NCI NIH HHS 2P01 CA065493NCI NIH HHS P01 CA065493NCI NIH HHS P30 CA077598NCI NIH HHS R01 CA072669NCI NIH HHS R01 CA081918NCI NIH HHS R01 CA 72669NHLBI NIH HHS T32 HL007062NIAID NIH HHS R01 AI081918
6 · The paper itself

Abstract

T lymphocytes are critical mediators of the adaptive immune system and have the capacity to serve as therapeutic agents in the areas of transplant and cancer immunotherapy. While T cells can be isolated and expanded from patients, T cells derived in vitro from both hematopoietic stem/progenitor cells (HSPCs) and human pluripotent stem cells (hPSCs) offer great potential advantages in generating a self-renewing source of T cells that can be readily genetically modified. T-cell differentiation in vivo is a complex process requiring tightly regulated signals; providing the correct signals in vitro to induce T-cell lineage commitment followed by their development into mature, functional, single positive T cells, is similarly complex. In this review, we discuss current methods for the in vitro derivation of T cells from murine and human HSPCs and hPSCs that use feeder-cell and feeder-cell-free systems. Furthermore, we explore their potential for adoption for use in T-cell-based therapies.

Indexed as

AdultAdult Stem CellsAnimalsCell DifferentiationEmbryonic Stem CellsHumansInduced Pluripotent Stem CellsPluripotent Stem CellsT-LymphocytesCD34 +Cell cultureCord bloodDifferentiationEmbryonic stem cellsHematopoietic stem cellsInduced pluripotent stem cellsT cells

Identifiers

PMID26227158
PMCPMC4762024

What OpenQuestion holds

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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.