Evidence map›Paper›PMID 36512410›Full record

ArticleJCI insight2023

Tumor cells fail to present MHC-II-restricted epitopes derived from oncogenes to CD4+ T cells.

Spencer E Brightman, Martin S Naradikian, Rukman R Thota, Angelica Becker, Leslie Montero, Milad Bahmanof, Ashmitaa Logandha Ramamoorthy Premlal, Jason A Greenbaum, Bjoern Peters, Ezra Ew Cohen and 2 more

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2023. 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
1.2field-weighted citation impact, top 22% 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

10 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. The spontaneous neoantigen-specific CD4Journal for immunotherapy of cancer · 2025
    Article
  5. Article
  6. Article
  7. Review
  8. Facts and Hopes in Immunotherapy Strategies Targeting Antigens Derived from KRAS Mutations.Clinical cancer research : an official journal of the American Association for Cancer Research · 2024
    Review
  9. Article
  10. 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

12 authors at 3 institutions in 2 countries.

Spencer E BrightmanDivision of Developmental Immunology, La Jolla Institute for Immunology, La Jolla, California, USA.
Martin S NaradikianDivision of Developmental Immunology, La Jolla Institute for Immunology, La Jolla, California, USA.
Rukman R ThotaDivision of Developmental Immunology, La Jolla Institute for Immunology, La Jolla, California, USA.
Angelica BeckerDivision of Developmental Immunology, La Jolla Institute for Immunology, La Jolla, California, USA.
Leslie MonteroDivision of Developmental Immunology, La Jolla Institute for Immunology, La Jolla, California, USA.
Milad BahmanofDivision of Developmental Immunology, La Jolla Institute for Immunology, La Jolla, California, USA.
Ashmitaa Logandha Ramamoorthy PremlalBioinformatics Core and.
Jason A GreenbaumBioinformatics Core and.
Bjoern PetersDivision of Vaccine Discovery, La Jolla Institute for Immunology, La Jolla, California, USA.
Ezra Ew CohenDivision of Hematology and Oncology, UCSD Moores Cancer Center, La Jolla, California, USA.
Aaron M MillerDivision of Developmental Immunology, La Jolla Institute for Immunology, La Jolla, California, USA.
Stephen P SchoenbergerDivision of Developmental Immunology, La Jolla Institute for Immunology, La Jolla, California, USA.
La Jolla Institute for Immunology · USGenomics Institute of the Novartis Research Foundation · USMoores Cancer Center

Funding

Stimulating Neo-Antigen Specific T Cell Responses in Head and Neck CancersU01DE028227 · NIDCR · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI GUTKIND, JORGE SILVIO, RAO, ANJANA · 2018 to 2022
$4.6M
NIDCR NIH HHS U01 DE028227
6 · The paper itself

Abstract

CD4+ T cells play a critical role in antitumor immunity via recognition of peptide antigens presented on MHC class II (MHC-II). Although some solid cancers can be induced to express MHC-II, the extent to which this enables direct recognition by tumor-specific CD4+ T cells is unclear. We isolated and characterized T cell antigen receptors (TCRs) from naturally primed CD4+ T cells specific for 2 oncoproteins, HPV-16 E6 and the activating KRASG12V mutation, from patients with head and neck squamous cell carcinoma and pancreatic ductal adenocarcinoma, respectively, and determined their ability to recognize autologous or human leukocyte antigen-matched antigen-expressing tumor cells. We found in both cases that the TCRs were capable of recognizing peptide-loaded target cells expressing the relevant MHC-II or B cell antigen-presenting cells (APCs) when the antigens were endogenously expressed and directed to the endosomal pathway but failed to recognize tumor cells expressing the source protein even after induction of surface MHC-II expression by IFN-γ or transduction with CIITA. These results suggest that priming and functional recognition of both a nuclear (E6) and a membrane-associated (KRAS) oncoprotein are predominantly confined to crosspresenting APCs rather than via direct recognition of tumor cells induced to express MHC-II.

Indexed as

CD4-Positive T-LymphocytesPancreatic NeoplasmsEpitopesHLA AntigensHumansOncogenesPeptidesReceptors, Antigen, T-CellEpitopesHLA AntigensPeptidesReceptors, Antigen, T-CellAntigen presentationCancer immunotherapyImmunologyOncologyT cell receptor

Identifiers

PMID36512410
PMCPMC9977289
OpenAlexW4311253232

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.