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Cytotoxic CD4+ T cells in cancer: Expanding the immune effector toolbox
Open accessAbstract
Cytotoxic T cells are important effectors of anti-tumor immunity. While tumor killing is ascribed to CD8 + T cell function, pre-clinical and clinical studies have identified intra-tumoral CD4 + T cells that possess cytotoxic programs and can directly kill cancer cells. Cytotoxic CD4 + T cells are found in other disease settings including infection and autoimmunity. Here, we review the phenotypic and functional characteristics of cytotoxic CD4 + T cells in non-cancer and cancer contexts. We conduct a comparative examination of cytolytic mechanisms of cytotoxic CD4 + T cells across disease states and synthesize features that define these cells independent of context. We discuss regulatory mechanisms driving ontogeny and effector function and evidence for the clinical relevance of cytotoxic CD4 + T cells in cancer. In this context, we highlight important gaps in understanding in the biology of cytotoxic CD4 + T cells as well as the potential use of these cells in immunotherapies for specific cancers.
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“we observed a significant increase in the total CD4+ T cells expressing IFN-γ (figure 4H) and granzyme B (GZMB; figure 4J),60–65 NK cells (figure 4N), and the amount of GZMB expression in CD8+ T cells (figure 4L) in the post-cryoablated RMS 76-9STINGwt TME as compared with RMS 76-9STING-/- TME in wild-type mice, as was Foxp3+ CD4+ cells (figure 4M).”
From Functional tumor cell-intrinsic STING, not host STING, drives local and systemic antitumor immunity and therapy efficacy following cryoablation (2023) · cites this paper as [64]
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TIGIT Blockade Reshapes the Tumor Microenvironment Based on the Single-cell RNA-Sequencing Analysis
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“Among them, HLA-DMB [46], HLA-DRA [47], IL12A, and IL12B [48], whose determinant role in cancer outcome as immune adjuvants has already been published, are found in the top 500 TG2 positively correlating genes.”
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“Although cytotoxic CD4 + T cells have been described [34], activated CD4 + T cells predominantly attract and support other immune cells within tumour draining lymph nodes and the tumour microenvironment (TME) [35].”
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“This finding is consistent with recent findings that CD4 cytotoxic T cells are also important for anti-tumor immunity and have potential use in immunotherapy for specific cancers [34].”
ResultThe Roles of RUNX Proteins in Lymphocyte Function and Anti-Tumor Immunity
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“3D), aligning with prior studies ( 23, 24 ).”
ResultFrouard, J., Telwatte, S., Luo, X., Elphick, N., Thomas, R., Arneson, D. V., Roychoudhury, P., Butte, A. J., Wong, J. K., Hoh, R., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.12.17.629023 · Cited by 5
“Active viral replication may promote the acquisition and maintenance of cytotoxic functions by CD4+ T cells by eliciting a sustained pro-inflammatory environment, which has been shown in the context of cancer 68 as well as during influenza infection 69 .”
Asymmetric Dimethylarginine Disrupts Tumor Antigen Presentation in Breast Cancer
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“This also provides a potential target for future clinical drug development [62].”
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Environmental Low-Dose Radiation Activates Th1 Immunity through the Mitochondria-STING Pathway
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Mutated DNMT3A creates a public HLADQ- binding neoantigen on acute myeloid leukemia
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“Some CD4 T cells are also capable of directly killing HLA class II-expressing tumor cells (25).”
Kim, H. J., JOO, B. K., BYUN, J.-S., & KIM, D.-Y. (2025) · Oncology Research Featuring Preclinical and Clinical Cancer Therapeutics · doi:10.32604/or.2025.062207 · Cited by 4
“While immunomodulatory strategies typically focus on bolstering tumor-in fi ltrating CD8+ T cell activity, CD4+ T cells also signi fi cantly in fl uence the TME by secreting cytokines that enhance CD8+ T cell in fi ltration [115].”
Li, W., Yang, G., Dong, H., Zhu, J., & Liu, T. (2022) · Frontiers in Medicine · doi:10.3389/fmed.2022.1055785 · Cited by 5
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“15 16 To date, how different forms of non-myeloablative preconditioning regimens impact the efficacy of transferred antitumor T helper cells has not been explored in a systematic manner.”
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Influential
Metadata
- Authors
- Oh, D. Y., & Fong, L.
- Affiliations
- University of California, San Francisco (US)
- Corresponding author
- Fong, Lawrence
- Venue
- Immunity
- Publisher
- Elsevier BV
- Published
- 2021-12
- Volume
- 54
- Issue
- 12
- Pages
- 2701-2711
- ISSN
- 1074-7613 (ISSN-L)
- PMC
- PMC8809482
- OpenAlex
- W4200244347
- Cited by
- 467
- References
- 73
- Citations by year
- 2026: 81 · 2025: 127 · 2024: 116 · 2023: 101 · 2022: 41 · 2021: 1
- FWCI
- 6.86
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Immunity (publishedVersion, cc-by)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion, cc-by)
- eScholarship (California Digital Library) (submittedVersion, cc-by)
- Funders
- NCI
- National Institutes of Health (K08AI139375)
- Prostate Cancer Foundation (R35CA253175)
- Bavarian Nordic
- Genentech
- Parker Institute for Cancer Immunotherapy
- AbbVie
- Amgen
- Merck
- Merck KGaA
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Health Sciences › Medicine › Oncology › Cancer Immunotherapy and Biomarkers
- Life Sciences › Immunology and Microbiology › Immunology › Immunotherapy and Immune Responses
- Keywords
- cytotoxic CD4+ T cells, antitumor immunity, cytotoxicity mechanism, cancer immunotherapy, infection, autoimmunity
- MeSH terms
- Animals, Cytotoxicity, Immunologic, Humans, Neoplasms, T-Lymphocytes, Cytotoxic, CD4-Positive T-Lymphocytes, Immunotherapy, Adoptive
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