Evidence map›Paper›PMID 20547105›Full record

ArticleClinical immunology (Orlando, Fla.)2010

MHC-I-restricted melanoma antigen specific TCR-engineered human CD4+ T cells exhibit multifunctional effector and helper responses, in vitro.

Swagatam Ray, Arvind Chhabra, Nitya G Chakraborty, Upendra Hegde, David I Dorsky, Thinle Chodon, Erika von Euw, Begonya Comin-Anduix, Richard C Koya, Antoni Ribas and 4 more

Abstract read
In one paragraph

Article in Clinical immunology (Orlando, Fla.), 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

22 citing papers in PubMed, 46 citations in OpenAlex.

  1. Article
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  4. Review
  5. Review
  6. Article
  7. Adaptive Resistance to Cancer Immunotherapy.Advances in experimental medicine and biology · 2017
    Review
  8. Human leucocyte antigen class I-redirected anti-tumour CD4Clinical and experimental immunology · 2017
    Article
  9. Strategies to genetically engineer T cells for cancer immunotherapy.Cancer immunology, immunotherapy : CII · 2016
    Review
  10. Article
  11. Review
  12. Review
  13. Review
  14. Article
  15. Review
  16. 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

14 authors at 4 institutions in 1 country.

Swagatam RayDepartment of Medicine, University of Connecticut Health Center, Farmington, CT 06030, USA.
Arvind Chhabra
Nitya G Chakraborty
Upendra Hegde
David I Dorsky
Thinle Chodon
Erika von Euw
Begonya Comin-Anduix
Richard C Koya
Antoni Ribas
James S Economou
Steven A Rosenberg
Bijay Mukherji
UCLA-CALTECH-CHLA-USC-UCONN Consortium on Translational Program in Engineered Immunity
UConn Health · USUniversity of California, Los Angeles · USUniversity of Southern California · USNational Cancer Institute · US

Funding

Adoptive Cell Transfer Immunotherapy of CancerZIABC010984 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI ROSENBERG, STEVEN · 2009 to 2025
$56.8M
ZONISAMIDE VERSUS PLACEBOM01RR006192 · NCRR · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI KRANZLER, HENRY RICHARD · 1994 to 2008
$22.1M
TCR Engineered CD4 Cells as Helpers in Tumor ImmunityR01CA088059 · NCI · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI MUKHERJI, BIJAY · 2001 to 2012
$2.0M
PET IMAGING OF MART TCR-ENGINEERED CD8 T CELL IMMUNOTHERAPY IN MANR01CA129816 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI ECONOMOU, JAMES S. · 2007 to 2011
$1.4M
T CELL RESPONSE TO GENETICALLY ENGINEERED AND MATURED DCR01CA083130 · NCI · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI MUKHERJI, BIJAY · 1999 to 2003
$956k
NCI NIH HHS CA 83130NCI NIH HHS R01 CA083130NCI NIH HHS R01 CA088059NCI NIH HHS R01 CA129816NCRR NIH HHS M01 RR006192
6 · The paper itself

Abstract

MHC class I-restricted human melanoma epitope MART-1(27-35) specific TCR-engineered CD4+CD25- T cells synthesize Th1 type cytokines and exhibit cytolytic effector function upon cognate stimulation. A detailed characterization of such TCR-engineered CD4+CD25- T cells now reveals that they are multifunctional. For example, they undergo multiple rounds of division, synthesize cytokines (IFN-gamma, TNF-alpha, IL-2, and MIP1ss), lyse target cells, and "help" the expansion of the MART-1(27-35) specific CD8+ T cells when stimulated by the MART-1(27-35) peptide pulsed DC. Multiparametric analyses reveal that a single TCR-engineered CD4+ T cell can perform as many as five different functions. Nearly 100% MART-1(27-35) specific TCR expressing CD4+ T cells can be generated through retroviral vector-based transduction and one round of in vitro stimulation by the peptide pulsed DC. MHC class I-restricted tumor epitope specific TCR transduced CD4+ T cells, therefore, could be useful in immunotherapeutic strategies for melanoma or other human malignancies.

Indexed as

CD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCell LineCell Line, TumorCell ProliferationEpitopesGenetic EngineeringHistocompatibility Antigens Class IHumansImmunotherapy, ActiveImmunotherapy, AdoptiveIn Vitro TechniquesLymphocyte ActivationMelanomaNeoplasm ProteinsReceptors, Antigen, T-CellEpitopesHistocompatibility Antigens Class IMART-1-Melan-A(27-35) epitopeNeoplasm ProteinsReceptors, Antigen, T-Cell

Identifiers

PMID20547105
PMCPMC2917536
OpenAlexW2001739592

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.