Evidence map›Paper›PMID 40187751›Full record

ArticleJournal for immunotherapy of cancer2025

MHC class II-mediated spontaneous rejection of breast carcinomas expressing model neoantigens.

James William Jenkins, Alvaro Peña, Sarah A Castro, Michael J Hansen, Virginia P Van Keulen, Sean T Foster, Pablo E Rios-Cruz, Joshua Yakubov, Destin T Hinson, Samuel M Olivier and 4 more

Abstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. 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

14 authors.

James William JenkinsDepartment of Immunology, Mayo Clinic, Rochester, Minnesota, USA.ORCID http://orcid.org/0000-0001-5694-9707
Alvaro PeñaDepartment of Immunology, Mayo Clinic, Rochester, Minnesota, USA.
Sarah A CastroDepartment of Immunology, Mayo Clinic, Rochester, Minnesota, USA.
Michael J HansenDepartment of Immunology, Mayo Clinic, Rochester, Minnesota, USA.
Virginia P Van KeulenDepartment of Immunology, Mayo Clinic, Rochester, Minnesota, USA.
Sean T FosterDepartment of Immunology, Mayo Clinic, Rochester, Minnesota, USA.
Pablo E Rios-CruzDepartment of Immunology, Mayo Clinic, Rochester, Minnesota, USA.
Joshua YakubovDepartment of Immunology, Mayo Clinic, Rochester, Minnesota, USA.
Destin T HinsonDepartment of Immunology, Mayo Clinic, Rochester, Minnesota, USA.
Samuel M OlivierDepartment of Immunology, Mayo Clinic, Rochester, Minnesota, USA.
Kevin D PavelkoDepartment of Immunology, Mayo Clinic, Rochester, Minnesota, USA.
Sara J FeltsDepartment of Immunology, Mayo Clinic, Rochester, Minnesota, USA.
Aaron J JohnsonDepartment of Immunology, Mayo Clinic, Rochester, Minnesota, USA.
Larry R PeaseDepartment of Immunology, Mayo Clinic, Rochester, Minnesota, USA pease.larry@mayo.edu.ORCID http://orcid.org/0000-0001-9770-1740

Funding

Women's Cancer ProgramP30CA015083 · NCI · MAYO CLINIC ROCHESTER · PI Lila J. Rutten · 1985 to 2026
$151.3M
TRAINING IN TRANSLATIONAL RESEARCH: BENCH TO BEDSIDER25GM055252 · NIGMS · MAYO CLINIC ROCHESTER · PI LUJAN, LUIS, MAHER, LOUIS JAMES · 1996 to 2022
$8.3M
NCI NIH HHS P30 CA015083NIGMS NIH HHS R25 GM055252
6 · The paper itself

Abstract

backgroundCancers persist despite expression of immunogenic neoantigens and ongoing antitumor immune responses. While some occult tumors likely are cleared by effective antitumor immune responses, the targeted antigens are not easily identifiable as those tumors spontaneously disappear.

methodsWe used mouse models with a defined antigenic protein mimicking tumor-specific neoantigens to address the nature of these spontaneous anti-tumor immune responses.

resultsBALB/c (

conclusionsWe find that the effective antitumor immunity targeting neoantigens in these breast cancer models is determined by MHC-II-restricted presentation of optimal cancer-associated antigens. These responses are dependent on CD4+ T cells, B cells, and antigen-specific antibodies.

Indexed as

Antigens, NeoplasmBreast NeoplasmsHistocompatibility Antigens Class IIMammary Neoplasms, ExperimentalAnimalsB-LymphocytesCD4-Positive T-LymphocytesCell Line, TumorDisease Models, AnimalErb-b2 Receptor Tyrosine KinasesFemaleHumansMiceMice, Inbred BALB CRatsAntigens, NeoplasmErbb2 protein, ratErb-b2 Receptor Tyrosine KinasesHistocompatibility Antigens Class IIAntibodyB cellMajor histocompatibility complex - MHCT cellTumor microenvironment - TME

Identifiers

PMID40187751
PMCPMC11973762

What Socratic holds

Textmetadata
LicenceCC BY-NC
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 Socratic graph.