Evidence map›Paper›PMID 26842125›Full record

ArticleCancer immunology, immunotherapy : CII2016

TCR gene-modified T cells can efficiently treat established hepatitis C-associated hepatocellular carcinoma tumors.

Timothy T Spear, Glenda G Callender, Jeffrey J Roszkowski, Kelly M Moxley, Patricia E Simms, Kendra C Foley, David C Murray, Gina M Scurti, Mingli Li, Justin T Thomas and 4 more

Abstract read
In one paragraph

Article 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. Review
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  10. Review
  11. APL bioengineering · 2021
    Review
  12. Cellular based immunotherapy for primary liver cancer.Journal of experimental & clinical cancer research : CR · 2021
    Review
  13. Article
  14. Review
  15. Article
  16. Review
  17. Article
  18. Review
  19. Engineering T cells for immunotherapy of primary human hepatocellular carcinoma.Journal of genetics and genomics = Yi chuan xue bao · 2020
    Review
  20. [Progress and prospects of clinical cell therapy for liver cirrhosis and liver cancer].Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2019
    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.

Timothy T SpearDepartment of Surgery, Cardinal Bernardin Cancer Center, Loyola University Chicago, 2160 S. 1st Ave, Maywood, IL, 60153, USA.
Glenda G CallenderDepartment of Surgery, University of Chicago, Chicago, IL, 60637, USA.
Jeffrey J RoszkowskiDepartment of Surgery, University of Chicago, Chicago, IL, 60637, USA.
Kelly M MoxleyDepartment of Surgery, Cardinal Bernardin Cancer Center, Loyola University Chicago, 2160 S. 1st Ave, Maywood, IL, 60153, USA.
Patricia E SimmsFlow Cytometry Core Facility, Cardinal Bernardin Cancer Center, Loyola University Chicago, Maywood, IL, 60153, USA.
Kendra C FoleyDepartment of Surgery, Cardinal Bernardin Cancer Center, Loyola University Chicago, 2160 S. 1st Ave, Maywood, IL, 60153, USA.
David C MurrayDepartment of Surgery, Cardinal Bernardin Cancer Center, Loyola University Chicago, 2160 S. 1st Ave, Maywood, IL, 60153, USA.
Gina M ScurtiDepartment of Surgery, Cardinal Bernardin Cancer Center, Loyola University Chicago, 2160 S. 1st Ave, Maywood, IL, 60153, USA.
Mingli LiDepartment of Surgery, Medical University of South Carolina, Charleston, SC, 29415, USA.
Justin T ThomasDepartment of Surgery, Cardinal Bernardin Cancer Center, Loyola University Chicago, 2160 S. 1st Ave, Maywood, IL, 60153, USA.
Alexander LangermanDepartment of Surgery, University of Chicago, Chicago, IL, 60637, USA.
Elizabeth Garrett-MayerDepartment of Public Health Sciences, Medical University of South Carolina, Charleston, SC, 29415, USA.
Yi ZhangDepartment of Surgery, Medical University of South Carolina, Charleston, SC, 29415, USA.
Michael I NishimuraDepartment of Surgery, Cardinal Bernardin Cancer Center, Loyola University Chicago, 2160 S. 1st Ave, Maywood, IL, 60153, USA. mnishimura@luc.edu.

Funding

TCR TRANSDUCED CDB T CELLS FOR ADOPTIVE IMMUNOTHERAPYP01CA154778 · NCI · LOYOLA UNIVERSITY CHICAGO · PI NISHIMURA, MICHAEL I. · 2011 to 2015
$15.4M
TCR Affinity and Therapeutic Efficacy of T CellsR01CA104947 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI NISHIMURA, MICHAEL I. · 2007 to 2011
$1.9M
Animal Model for Her-2/neu Specific TCR Gene TransferR01CA102280 · NCI · UNIVERSITY OF CHICAGO · PI NISHIMURA, MICHAEL I · 2003 to 2007
$1.4M
Tumor Recognition by TCR Transduced CD4+ and CD8+T CellsR01CA090873 · NCI · UNIVERSITY OF CHICAGO · PI NISHIMURA, MICHAEL I · 2001 to 2004
$1.3M
TCR Engineering of Quiescent Primary Human T CellsR21CA153789 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI NISHIMURA, MICHAEL I. · 2010 to 2011
$348k
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 CA090873NCI NIH HHS R01 CA102280NCI NIH HHS R01 CA104947NCI NIH HHS R01 CA104947-S1NCI NIH HHS R01 CA90873NCI NIH HHS R21 CA153789
6 · The paper itself

Abstract

The success in recent clinical trials using T cell receptor (TCR)-genetically engineered T cells to treat melanoma has encouraged the use of this approach toward other malignancies and viral infections. Although hepatitis C virus (HCV) infection is being treated with a new set of successful direct anti-viral agents, potential for virologic breakthrough or relapse by immune escape variants remains. Additionally, many HCV+ patients have HCV-associated disease, including hepatocellular carcinoma (HCC), which does not respond to these novel drugs. Further exploration of other approaches to address HCV infection and its associated disease are highly warranted. Here, we demonstrate the therapeutic potential of PBL-derived T cells genetically engineered with a high-affinity, HLA-A2-restricted, HCV NS3:1406-1415-reactive TCR. HCV1406 TCR-transduced T cells can recognize naturally processed antigen and elicit CD8-independent recognition of both peptide-loaded targets and HCV+ human HCC cell lines. Furthermore, these cells can mediate regression of established HCV+ HCC in vivo. Our results suggest that HCV TCR-engineered antigen-reactive T cells may be a plausible immunotherapy option to treat HCV-associated malignancies, such as HCC.

Indexed as

AnimalsCarcinoma, HepatocellularCell Line, TumorDEAD-box RNA HelicasesGenes, T-Cell ReceptorGenetic EngineeringHepatitis CHLA-A2 AntigenHumansImmunotherapyLiver NeoplasmsMiceNucleoside-TriphosphataseSerine EndopeptidasesT-LymphocytesViral Nonstructural ProteinsDEAD-box RNA HelicasesHLA-A2 AntigenNS3 protein, hepatitis C virusNucleoside-TriphosphataseSerine EndopeptidasesViral Nonstructural ProteinsViral ProteasesAdoptive cell transferCancerHepatitis C virusHepatocellular carcinomaT cellT cell receptor

Identifiers

PMID26842125
PMCPMC4887146

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.