Evidence map›Paper›PMID 33256913›Full record

ArticleSeminars in hematology2020

Genetic and epigenetic modification of human primary NK cells for enhanced antitumor activity.

Meisam Naeimi Kararoudi, Brian P Tullius, Nitin Chakravarti, Emily J Pomeroy, Branden S Moriarity, Kathie Beland, Aurelien B L Colamartino, Elie Haddad, Yaya Chu, Mitchell S Cairo and 1 more

Open access · greenAbstract read
In one paragraph

Article in Seminars in hematology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.4field-weighted citation impact, top 15% 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

16 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
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  3. Review
  4. Article
  5. Systemic Immunomodulatory Effects ofInternational journal of molecular sciences · 2023
    Article
  6. Article
  7. Natural Killer Cell-Based Immunotherapy against Glioblastoma.International journal of molecular sciences · 2023
    Review
  8. Article
  9. Review
  10. Review
  11. Article
  12. Review
  13. Review
  14. Review
  15. Nonviral genome engineering of natural killer cells.Stem cell research & therapy · 2021
    Review
  16. 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

11 authors at 5 institutions in 2 countries.

Meisam Naeimi KararoudiCenter for Childhood Cancer and Blood Disorders, Abigail Wexner Research Institute of Nationwide Children's Hospital, Columbus, OH.
Brian P TulliusCenter for Childhood Cancer and Blood Disorders, Abigail Wexner Research Institute of Nationwide Children's Hospital, Columbus, OH.
Nitin ChakravartiDepartment of Medical Oncology, Thomas Jefferson University, Philadelphia, PA.
Emily J PomeroyCenter for Genome Engineering, University of Minnesota, Minneapolis, MN.
Branden S MoriarityCenter for Genome Engineering, University of Minnesota, Minneapolis, MN.
Kathie BelandCHU Sainte-Justine Research Center, Montréal, QC, Canada.
Aurelien B L ColamartinoCHU Sainte-Justine Research Center, Montréal, QC, Canada.
Elie HaddadCHU Sainte-Justine Research Center, Montréal, QC, Canada.
Yaya ChuDepartment of Pediatrics, New York Medical College, Valhalla, NY.
Mitchell S CairoDepartment of Pediatrics, New York Medical College, Valhalla, NY.
Dean A LeeCenter for Childhood Cancer and Blood Disorders, Abigail Wexner Research Institute of Nationwide Children's Hospital, Columbus, OH. Electronic address: dean.lee@nationwidechildrens.org.
Centre Hospitalier Universitaire Sainte-Justine · CANationwide Children's Hospital · USNew York Medical College · USUniversity of Minnesota · USThomas Jefferson University · US

Funding

IMMUNOLOGY TRAINING PROGRAMT32AI007313 · NIAID · UNIVERSITY OF MINNESOTA TWIN CITIES · PI Carla Rothlin · 1989 to 2026
$5.7M
Genetically Modified Natural Killer Cells for Cancer ImmunotherapyR21CA216652 · NCI · UNIVERSITY OF MINNESOTA · PI MORIARITY, BRANDEN S · 2018 to 2019
$362k
NCI NIH HHS R21 CA216652NIAID NIH HHS T32 AI007313
6 · The paper itself

Abstract

Cancer immunotherapy using genetically modified immune cells such as those expressing chimeric antigen receptors has shown dramatic outcomes in patients with refractory and relapsed malignancies. Natural killer (NK) cells as a member of the innate immune system, possessing both anticancer (cytotoxic) and proinflammatory (cytokine) responses to cancers and rare off-target toxicities have great potential for a wide range of cancer therapeutic settings. Therefore, improving NK cell antitumor activity through genetic modification is of high interest in the field of cancer immunotherapy. However, gene manipulation in primary NK cells has been challenging because of broad resistance to many genetic modification methods that work well in T cells. Here we review recent successful approaches for genetic and epigenetic modification of NK cells including epigenetic remodeling, transposons, mRNA-mediated gene delivery, lentiviruses, and CRISPR gene targeting.

Indexed as

AnimalsDisease Models, AnimalEpigenesis, GeneticGenetic TherapyHumansImmunotherapyKiller Cells, NaturalMiceNeoplasmsCancer immunotherapyCRISPRGenetic modificationNatural killer cellsTransposonsViral vectors

Identifiers

PMID33256913
PMCPMC7809645
OpenAlexW3099890097

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.