Evidence map›Paper›PMID 41436233›Full record

ReviewJournal for immunotherapy of cancer2025

Cytotoxic CD4+ T cells in cancer: an emerging target for next-generation anticancer immunotherapy?

Imke M B van Wandeloo, Kalijn Bol, Carla van Herpen, I Jolanda M de Vries, Gerty Schreibelt

Abstract readReview
In one paragraph

Review 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. Article
  3. Article
  4. 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

5 authors.

Imke M B van WandelooMedical Oncology, Radboudumc, Nijmegen, Gelderland, The Netherlands.
Kalijn BolMedical Oncology, Radboudumc, Nijmegen, Gelderland, The Netherlands.ORCID http://orcid.org/0000-0003-4165-2040
Carla van HerpenMedical Oncology, Radboudumc, Nijmegen, Gelderland, The Netherlands.
I Jolanda M de VriesMedical BioSciences, Radboudumc, Nijmegen, Gelderland, The Netherlands jolanda.devries@radboudumc.nl.ORCID http://orcid.org/0000-0002-8653-4040
Gerty SchreibeltMedical BioSciences, Radboudumc, Nijmegen, Gelderland, The Netherlands.ORCID http://orcid.org/0000-0002-0156-8365

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Over the last decades, a growing number of distinct CD4+T helper cells has been identified and our understanding of CD4+T cell differentiation and function in various disease contexts has increased immensely. It has long been thought that the role of CD4+T cells in the tumor microenvironment (TME) was limited to coordinating the immune response by stimulating other immune cells and by secretion of cytokines with antitumor activity, while direct killing of tumor cells has been largely attributed to cytotoxic CD8+T cells. Notably, CD4+T cells with direct cytotoxic activity (CD4+CTLs) have been reported in the context of viral infections, autoimmune disorders, and more recently in patients with various cancer types. These cells have the ability to secrete cytotoxic molecules and kill target cells in a major histocompatibility complex (MHC) class II-dependent manner. In this review, we give an overview of phenotypical characteristics of CD4+CTLs in human cancers and the antitumor mechanisms employed by these cells. Further, we explore their role and clinical relevance in the context of cancer and describe how these cells may be used for the development of novel immunotherapeutic options to benefit patients with cancer with MHC class II-positive tumors.

Indexed as

CD4-Positive T-LymphocytesImmunotherapyNeoplasmsT-Lymphocytes, CytotoxicAnimalsHumansTumor MicroenvironmentImmunotherapyT cell

Identifiers

PMID41436233
PMCPMC12730827

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.