Evidence map›Paper›PMID 34571290›Full record

ReviewCurrent opinion in immunology2022

Synthetic receptors for logic gated T cell recognition and function.

Sylvain Simon, Grace Bugos, Alex I Salter, Stanley R Riddell

Abstract readReview
In one paragraph

Review in Current opinion in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Cellular immunotherapy in melanoma: the next frontier in cancer treatment.Journal of experimental & clinical cancer research : CR · 2026
    Review
  2. Review
  3. Review
  4. CAR-T cell therapy for cancer: current challenges and future directions.Signal transduction and targeted therapy · 2025
    Review
  5. Review
  6. Advances in CAR-T-cell therapy in T-cell malignancies.Journal of hematology & oncology · 2024
    Review
  7. T cells in health and disease.Signal transduction and targeted therapy · 2023
    Review
  8. Review
  9. Article
  10. Visualizing cell-cell communication using synthetic notch activated MRI.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
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

4 authors.

Sylvain SimonFred Hutchinson Cancer Research Center, Seattle, WA, United States.
Grace BugosFred Hutchinson Cancer Research Center, Seattle, WA, United States; Department of Immunology, University of Washington, Seattle, WA, United States.
Alex I SalterFred Hutchinson Cancer Research Center, Seattle, WA, United States; Department of Medicine, University of Washington, Seattle, WA, United States.
Stanley R RiddellFred Hutchinson Cancer Research Center, Seattle, WA, United States; Department of Immunology, University of Washington, Seattle, WA, United States; Department of Medicine, University of Washington, Seattle, WA, United States. Electronic address: sriddell@fredhutch.org.

Funding

TARGETING ROR1 WITH CHIMERIC ANTIGEN RECEPTOR MODIFIED T CELLSR01CA114536 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Sylvain Simon · 2005 to 2026
$8.4M
NCI NIH HHS R01 CA114536
6 · The paper itself

Abstract

Adoptive cell therapy with T cells engineered with customized receptors that redirect antigen specificity to cancer cells has emerged as an effective therapeutic approach for many malignancies. Toxicity due to on target or off target effects, antigen heterogeneity on cancer cells, and acquired T cell dysfunction have been identified as barriers that can hinder successful therapy. This review will discuss recent advances in T cell engineering that have enabled the application of logic gates in T cells that can mimic the integration of natural signaling pathways and act in a cell intrinsic or extrinsic fashion to precisely target tumor cells and regulate effector functions, potentially overcoming these barriers to effective therapy.

Indexed as

NeoplasmsReceptors, ArtificialAntigensHumansImmunotherapy, AdoptiveReceptors, Antigen, T-CellT-LymphocytesAntigensReceptors, Antigen, T-CellReceptors, Artificial

Identifiers

PMID34571290
PMCPMC8901444

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.