Evidence map›Paper›PMID 22926060›Full record

ArticleCancer immunology, immunotherapy : CII2013

MHC-class I-restricted CD4 T cells: a nanomolar affinity TCR has improved anti-tumor efficacy in vivo compared to the micromolar wild-type TCR.

Carolina M Soto, Jennifer D Stone, Adam S Chervin, Boris Engels, Hans Schreiber, Edward J Roy, David M Kranz

Abstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

24 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. T cell receptor specificity landscape revealed through de novo peptide design.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  3. Article
  4. Article
  5. Article
  6. What's the Catch? The Significance of Catch Bonds in T Cell Activation.Journal of immunology (Baltimore, Md. : 1950) · 2023
    Review
  7. Article
  8. Review
  9. Article
  10. Review
  11. Review
  12. A rare population of tumor antigen-specific CD4Journal for immunotherapy of cancer · 2019
    Article
  13. Review
  14. Human leucocyte antigen class I-redirected anti-tumour CD4Clinical and experimental immunology · 2017
    Article
  15. Article
  16. Article
  17. Review
  18. New Strategies in Engineering T-cell Receptor Gene-Modified T cells to More Effectively Target Malignancies.Clinical cancer research : an official journal of the American Association for Cancer Research · 2015
    Review
  19. Article
  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

7 authors at 2 institutions in 1 country.

Carolina M SotoNeuroscience Program, University of Illinois, Urbana, IL 61801, USA.
Jennifer D Stone
Adam S Chervin
Boris Engels
Hans Schreiber
Edward J Roy
David M Kranz
University of Illinois Urbana-Champaign · USUniversity of Chicago · US

Funding

Protein Expression and Peptide CoreP01CA097296 · NCI · UNIVERSITY OF CHICAGO · PI SCHREIBER, HANS · 2003 to 2012
$15.0M
NCI NIH HHS CA097296NCI NIH HHS P01 CA097296
6 · The paper itself

Abstract

Clinical studies with immunotherapies for cancer, including adoptive cell transfers of T cells, have shown promising results. It is now widely believed that recruitment of CD4(+) helper T cells to the tumor would be favorable, as CD4(+) cells play a pivotal role in cytokine secretion as well as promoting the survival, proliferation, and effector functions of tumor-specific CD8(+) cytotoxic T lymphocytes. Genetically engineered high-affinity T-cell receptors (TCRs) can be introduced into CD4(+) helper T cells to redirect them to recognize MHC-class I-restricted antigens, but it is not clear what affinity of the TCR will be optimal in this approach. Here, we show that CD4(+) T cells expressing a high-affinity TCR (nanomolar K (d) value) against a class I tumor antigen mediated more effective tumor treatment than the wild-type affinity TCR (micromolar K (d) value). High-affinity TCRs in CD4(+) cells resulted in enhanced survival and long-term persistence of effector memory T cells in a melanoma tumor model. The results suggest that TCRs with nanomolar affinity could be advantageous for tumor targeting when expressed in CD4(+) T cells.

Indexed as

Adoptive TransferAnimalsAntigens, NeoplasmAntineoplastic AgentsCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCell Line, TumorCell SurvivalGenes, MHC Class IHistocompatibility Antigens Class IInterferon-gammaMelanoma, ExperimentalMiceMice, Inbred C57BLReceptors, Antigen, T-CellSkin NeoplasmsAntigens, NeoplasmAntineoplastic AgentsHistocompatibility Antigens Class IInterferon-gammaReceptors, Antigen, T-Cell

Identifiers

PMID22926060
PMCPMC3570684
OpenAlexW2062807307

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.