Evidence map›Paper›PMID 27138532›Full record

ReviewCancer immunology, immunotherapy : CII2016

Strategies to genetically engineer T cells for cancer immunotherapy.

Timothy T Spear, Kaoru Nagato, Michael I Nishimura

Abstract readReview
In one paragraph

Review in Cancer immunology, immunotherapy : CII, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing 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

35 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Review
  6. Endocrine, metabolic & immune disorders drug targets · 2024
    Article
  7. Review
  8. Review
  9. Review
  10. Review
  11. Review
  12. Article
  13. Review
  14. Review
  15. Article
  16. Assessment of Current Gene Therapy Practices in Hepatocellular Carcinoma.Gastrointestinal disorders (Basel, Switzerland) · 2020
    Article
  17. Immune cell engineering: opportunities in lung cancer therapeutics.Drug delivery and translational research · 2020
    Review
  18. Review
  19. Review
  20. 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

3 authors.

Timothy T SpearDepartment of Surgery, Cardinal Bernardin Cancer Center, Loyola University Medical Center, Loyola University Chicago, 2160 S. 1st Ave, Bldg 112, Room 308, Maywood, IL, 60153, USA. tspear@luc.edu.
Kaoru NagatoDepartment of Surgery, Cardinal Bernardin Cancer Center, Loyola University Medical Center, Loyola University Chicago, 2160 S. 1st Ave, Bldg 112, Room 308, Maywood, IL, 60153, USA.
Michael I NishimuraDepartment of Surgery, Cardinal Bernardin Cancer Center, Loyola University Medical Center, Loyola University Chicago, 2160 S. 1st Ave, Bldg 112, Room 308, Maywood, IL, 60153, USA.

Funding

TCR TRANSDUCED CDB T CELLS FOR ADOPTIVE IMMUNOTHERAPYP01CA154778 · NCI · LOYOLA UNIVERSITY CHICAGO · PI NISHIMURA, MICHAEL I. · 2011 to 2015
$15.4M
Tumor Recognition by TCR Transduced CD4+ and CD8+T CellsR01CA090873 · NCI · UNIVERSITY OF CHICAGO · PI NISHIMURA, MICHAEL I · 2001 to 2004
$1.3M
TCR Gene Transfer for Treating HCV-Associated MalignanciesF30CA180731 · NCI · LOYOLA UNIVERSITY CHICAGO · PI SPEAR, TIMOTHY · 2014 to 2018
$154k
NCI NIH HHS F30 CA180731NCI NIH HHS P01 CA154778NCI NIH HHS R01 CA090873
6 · The paper itself

Abstract

Immunotherapy is one of the most promising and innovative approaches to treat cancer, viral infections, and other immune-modulated diseases. Adoptive immunotherapy using gene-modified T cells is an exciting and rapidly evolving field. Exploiting knowledge of basic T cell biology and immune cell receptor function has fostered innovative approaches to modify immune cell function. Highly translatable clinical technologies have been developed to redirect T cell specificity by introducing designed receptors. The ability to engineer T cells to manifest desired phenotypes and functions is now a thrilling reality. In this review, we focus on outlining different varieties of genetically engineered T cells, their respective advantages and disadvantages as tools for immunotherapy, and their promise and drawbacks in the clinic.

Indexed as

Genetic EngineeringImmunotherapyAnimalsAntigens, NeoplasmClinical Trials as TopicCytokinesHumansImmunotherapy, AdoptiveMiceNeoplasmsReceptors, Antigen, T-CellRecombinant Fusion ProteinsT-LymphocytesTreatment OutcomeAntigens, NeoplasmCytokinesReceptors, Antigen, T-CellRecombinant Fusion ProteinsAdoptive cell therapyChimeric antigen receptor (CAR)Gene-modified T cellsT cellT cell receptor (TCR)Tumor immunity

Identifiers

PMID27138532
PMCPMC5424608

What OpenQuestion holds

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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.