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Paper · 39160299

A synthetic cytotoxic T cell platform for rapidly prototyping TCR function.

Sharma G and 6 others. NPJ Precis Oncol, 2024. Cited by 3 papers, by iCite.

11 sourcespapers-2026-11-12-0.1.0

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ConductScience Library. A synthetic cytotoxic T cell platform for rapidly prototyping TCR function. Papers, record 39160299. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/39160299

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Paper

PubMed's record of the paper, with iCite's citation figures. No abstract is shown.

Title
A synthetic cytotoxic T cell platform for rapidly prototyping TCR function.
PubMed
Journal
NPJ Precis Oncol
PubMed
Year
2024
PubMed
Publication types
Journal Article
PubMed
Citations, by iCite
3
iCite
Relative citation ratio, by iCite
0.26, provisional
iCite
Revised in PubMed
2024-08-27
PubMed

Authors7

The authors in the order PubMed's record lists them, with the ORCID iDs it states.

OrderAuthorForenameKindORCID iD
1Sharma GGovindahttps://orcid.org/0000-0002-5675-2637
2Round JJames
3Teng FFei
4Ali ZZahra
5May CChris
6Yung EEric
7Holt RARobert Ahttps://orcid.org/0000-0002-7259-1247

Source PubMed

Topics0

NLM's MeSH indexing of the paper, its major topics first.

None in this release.

Grants5

Each grant PubMed's record writes, matched to the NIH project NIH's grant and paper links name for this paper, and each of those links the record does not write.

Grant, as the record writes itAgencyCountryNIH projectStated bySource
I2C2020Michael Smith Foundation for Health Research (MSFHR)PubMedPubMed
I2C2021Michael Smith Foundation for Health Research (MSFHR)PubMedPubMed
R21 CA226321NCI NIH HHSUnited StatesR21CA226321PubMed and NIHNIH RePORTER
PIF005Genome British ColumbiaPubMedPubMed
1R21CA226321-01U.S. Department of Health & Human Services | NIH | National Cancer Institute (NCI)R21CA226321PubMed and NIHNIH RePORTER

Trials0

The trials whose ClinicalTrials.gov record lists the paper, and the trial numbers the paper's PubMed record names.

None in this release.

Comments and corrections1

PubMed's comments and corrections, NLM's own indexing: retractions first, then expressions of concern, errata and updates, and comments last.

KindPMIDTitleIn Papers
Update of38,045,272

Source PubMed

References64

The papers the reference list in PubMed's record names, those in our copy of PubMed, in the list's order.

OrderPMIDTitleJournalYearIn PapersSource
122,484,809Unbiased identification of target antigens of CD8+ T cells with combinatorial libraries coding for short peptides.Nat Med2012https://conductscience.org/library/papers/22484809PubMed
232,816,891Tebentafusp, A TCR/Anti-CD3 Bispecific Fusion Protein Targeting gp100, Potently Activated Antitumor Immune Responses in Patients with Metastatic Melanoma.Clin Cancer Res2020https://conductscience.org/library/papers/32816891PubMed
315,057,788Jurkat T cells and development of the T-cell receptor signalling paradigm.Nat Rev Immunol2004https://conductscience.org/library/papers/15057788PubMed
427,959,684T-Cell Transfer Therapy Targeting Mutant KRAS in Cancer.N Engl J Med2016https://conductscience.org/library/papers/27959684PubMed
522,044,041Structural and biophysical determinants of αβ T-cell antigen recognition.Immunology2012https://conductscience.org/library/papers/22044041PubMed
624,323,902Surveillance of the tumor mutanome by T cells during progression from primary to recurrent ovarian cancer.Clin Cancer Res2014https://conductscience.org/library/papers/24323902PubMed
729,944,754iReceptor: A platform for querying and analyzing antibody/B-cell and T-cell receptor repertoire data across federated repositories.Immunol Rev2018https://conductscience.org/library/papers/29944754PubMed
830,190,323Natural killer cells induce distinct modes of cancer cell death: Discrimination, quantification, and modulation of apoptosis, necrosis, and mixed forms.J Biol Chem2018https://conductscience.org/library/papers/30190323PubMed
932,226,429Tumor-Infiltrating T Cells From Clear Cell Renal Cell Carcinoma Patients Recognize Neoepitopes Derived From Point and Frameshift Mutations.Front Immunol2020https://conductscience.org/library/papers/32226429PubMed
1036,589,698A library of cancer testis specific T cell receptors for T cell receptor gene therapy.Mol Ther Oncolytics2023https://conductscience.org/library/papers/36589698PubMed

1 to 10 of 64

See all 64 references

Cited by2

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 3 citations.

PMIDTitleJournalYearIn PapersSource
41,562,097Comprehensive self-antigen screening to assess cross-reactivity in promiscuous T-cell receptors.Front Immunol2025https://conductscience.org/library/papers/41562097PubMed
40,481,101RAN potentiates nuclear export of phosphorylated AMPK, reshaping lipid metabolism and impairing immune efficacy in lung adenocarcinoma.NPJ Precis Oncol2025https://conductscience.org/library/papers/40481101PubMed

Genes3

The genes the Gene search release ties to the paper: Swiss-Prot's references first, then PubTator's text mining.

GeneNCBI Gene IDLinked byIn GenesSource
HLA-A3,105PubTator's text mininghttps://conductscience.org/library/genes/3105NCBI Gene
HLA-C3,107PubTator's text mininghttps://conductscience.org/library/genes/3107NCBI Gene
TRBV20OR9-26,962PubTator's text mininghttps://conductscience.org/library/genes/6962NCBI Gene

Drugs0

The drugs whose trials, in the Pipelines release, list the paper.

None in this release.

Data0

The data bank entries PubMed's record names. Trial numbers are under Trials.

None in this release.

Data dates

The date of each source this release read.

PubMed
2026-11-06
PubMed
iCite
2026-11-05
iCite
PMC's ID file
2026-11-05
PMC's ID file
NIH RePORTER's grant and paper links
2026-11-01
NIH RePORTER's grant and paper links
Trials
2026-11-12
Gene search
2026-11-11
Pipelines
2026-09-18

Sources 11

  • ChEMBL, through Open TargetsCC BY-SA 3.0
  • ClinicalTrials.govNo license stated
  • HGNCCC0
  • iCiteCC BY 4.0
  • NCBI GenePublic domain (US government)
  • NIH RePORTER's grant and paper linksPublic domain
  • Open TargetsCC0 1.0
  • PMC's ID filePublic domain (US government)
  • PubMedNLM's terms
  • PubTator 3Public domain
  • UniProtCC BY 4.0
Each source's terms
  • ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
  • ClinicalTrials.govnone stated
  • HGNCCC0: https://www.genenames.org/about/license/
  • iCiteCC BY 4.0
  • NCBI GeneNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
  • NIH RePORTER's grant and paper linksPublic domain (NIH RePORTER)
  • Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
  • PMC's ID fileNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
  • PubMedNLM's terms
  • PubTator 3Public domain
  • UniProtCC BY 4.0. UniProt's licence file: "All databases and documents in the UniProt FTP directory may be copied and redistributed freely, without advance permission, provided that this copyright statement is reproduced with each copy." UniProt asks that users cite its latest paper: The UniProt Consortium, UniProt: the Universal Protein Knowledgebase in 2025, Nucleic Acids Research 53:D609-D617, https://doi.org/10.1093/nar/gkae1010. Read on 9 Nov 2026 at https://www.uniprot.org/help/license

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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