Evidence map›Paper›PMID 29235195›Full record

ReviewStem cells (Dayton, Ohio)2018

Concise Review: Human Pluripotent Stem Cells to Produce Cell-Based Cancer Immunotherapy.

Huang Zhu, Yi-Shin Lai, Ye Li, Robert H Blum, Dan S Kaufman

Abstract readReview
In one paragraph

Review in Stem cells (Dayton, Ohio), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing 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

25 citing papers in PubMed.

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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

5 authors.

Huang ZhuDepartment of Medicine, Division of Regenerative Medicine, University of California San Diego, San Diego, California, USA.
Yi-Shin LaiDepartment of Medicine, Division of Regenerative Medicine, University of California San Diego, San Diego, California, USA.
Ye LiDepartment of Medicine, Division of Regenerative Medicine, University of California San Diego, San Diego, California, USA.
Robert H BlumDepartment of Medicine, Division of Regenerative Medicine, University of California San Diego, San Diego, California, USA.
Dan S KaufmanDepartment of Medicine, Division of Regenerative Medicine, University of California San Diego, San Diego, California, USA.ORCID 0000-0002-2003-2494

Funding

A Rational Systematic Approach to Find Combinations of Pharmacologic and Immune Therapies that Target Identifiable Oncogenic StatesU01CA217885 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI COHEN, EZRA, KAUFMAN, DAN S. · 2017 to 2021
$5.1M
Expression of recombinant Fc receptors by engineered NK cells to enhance cancer cell killingR01CA203348 · NCI · UNIVERSITY OF MINNESOTA · PI WALCHECK, BRUCE K, WU, JIANMING · 2016 to 2025
$4.4M
NCI NIH HHS R01 CA203348NCI NIH HHS U01 CA217885
6 · The paper itself

Abstract

Human pluripotent stem cells (PSCs) provide a promising resource to produce immune cells for adoptive cellular immunotherapy to better treat and potentially cure otherwise lethal cancers. Cytotoxic T cells and natural killer (NK) cells can now be routinely produced from human PSCs. These PSC-derived lymphocytes have phenotype and function similar to primary lymphocytes isolated from peripheral blood. PSC-derived T and NK cells have advantages compared with primary immune cells, as they can be precisely engineered to introduce improved anti-tumor activity and produced in essentially unlimited numbers. Stem Cells 2018;36:134-145.

Indexed as

HumansImmunotherapyKiller Cells, NaturalLymphocytesPluripotent Stem CellsT-Lymphocytes, CytotoxicAdoptive cell therapyCancer immunotherapyHuman pluripotent stem cellNatural Killer cellNatural Killer T cellT cell

Identifiers

PMID29235195
PMCPMC5914526

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.