Evidence map›Paper›PMID 35474673›Full record

ArticleCell reports methods2021

Systematic discovery and validation of T cell targets directed against oncogenic KRAS mutations.

Jaewon Choi, Scott P Goulding, Brandon P Conn, Christopher D McGann, Jared L Dietze, Jessica Kohler, Divya Lenkala, Antoine Boudot, Daniel A Rothenberg, Paul J Turcott and 8 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports methods, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
3.1field-weighted citation impact, top 7% 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

51 citing papers in PubMed, 61 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Computational Methods for Cancer Neoantigen Prediction.Methods in molecular biology (Clifton, N.J.) · 2026
    Article
  10. Review
  11. Article
  12. A KRASMolecular therapy. Oncology · 2025
    Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. An Engineered Soluble Single-Chain TCR Engager for KRAS-G12V Specific Tumor Immunotherapy.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  18. Article
  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

18 authors at 1 institution in 1 country.

Jaewon ChoiBioNTech US Inc., 40 Erie Street, Suite 110, Cambridge, MA 02139, USA.
Scott P GouldingBioNTech US Inc., 40 Erie Street, Suite 110, Cambridge, MA 02139, USA.
Brandon P ConnBioNTech US Inc., 40 Erie Street, Suite 110, Cambridge, MA 02139, USA.
Christopher D McGannBioNTech US Inc., 40 Erie Street, Suite 110, Cambridge, MA 02139, USA.
Jared L DietzeBioNTech US Inc., 40 Erie Street, Suite 110, Cambridge, MA 02139, USA.
Jessica KohlerBioNTech US Inc., 40 Erie Street, Suite 110, Cambridge, MA 02139, USA.
Divya LenkalaBioNTech US Inc., 40 Erie Street, Suite 110, Cambridge, MA 02139, USA.
Antoine BoudotBioNTech US Inc., 40 Erie Street, Suite 110, Cambridge, MA 02139, USA.
Daniel A RothenbergBioNTech US Inc., 40 Erie Street, Suite 110, Cambridge, MA 02139, USA.
Paul J TurcottBioNTech US Inc., 40 Erie Street, Suite 110, Cambridge, MA 02139, USA.
John R SroujiBioNTech US Inc., 40 Erie Street, Suite 110, Cambridge, MA 02139, USA.
Kendra C FoleyBioNTech US Inc., 40 Erie Street, Suite 110, Cambridge, MA 02139, USA.
Michael S RooneyBioNTech US Inc., 40 Erie Street, Suite 110, Cambridge, MA 02139, USA.
Marit M van BuurenBioNTech US Inc., 40 Erie Street, Suite 110, Cambridge, MA 02139, USA.
Richard B GaynorBioNTech US Inc., 40 Erie Street, Suite 110, Cambridge, MA 02139, USA.
Jennifer G AbelinBioNTech US Inc., 40 Erie Street, Suite 110, Cambridge, MA 02139, USA.
Terri A AddonaBioNTech US Inc., 40 Erie Street, Suite 110, Cambridge, MA 02139, USA.
Vikram R JunejaBioNTech US Inc., 40 Erie Street, Suite 110, Cambridge, MA 02139, USA.
BioNTech (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Oncogenic mutations in KRAS can be recognized by T cells on specific class I human leukocyte antigen (HLA-I) molecules, leading to tumor control. To date, the discovery of T cell targets from KRAS mutations has relied on occasional T cell responses in patient samples or the use of transgenic mice. To overcome these limitations, we have developed a systematic target discovery and validation pipeline. We evaluate the presentation of mutant KRAS peptides on individual HLA-I molecules using targeted mass spectrometry and identify 13 unpublished KRAS

Indexed as

Lung NeoplasmsT-LymphocytesAnimalsHistocompatibility Antigens Class IHumansMiceMutationProto-Oncogene Proteins p21(ras)Receptors, Antigen, T-CellHistocompatibility Antigens Class IKRAS protein, humanProto-Oncogene Proteins p21(ras)Receptors, Antigen, T-CellcancerHLAimmunotherapymass spectrometryneoantigenPRMRAST cellTCR

Identifiers

PMID35474673
PMCPMC9017224
OpenAlexW3199819202

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.