Cited by 476T-cell and B-cell ImmunologyCancer Immunotherapy and BiomarkersImmunotherapy and Immune Responses

The DOI matches its Crossref record; 72 of the 73 references it cites were found in a registry or an index.

Cytotoxic CD4+ T cells in cancer: Expanding the immune effector toolbox

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Oh, David Y., Fong, Lawrence·2021·Immunity

Abstract

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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Crossref · 10.1016/j.immuni.2021.11.015

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Figures

Figure 1. The ontogeny and regulation of cytotoxic CD4+ T cells in cancer (A) A schematic of known CD4+ T cell functional subtypes, the cytokines that promote their differentiation, and master transcription factors (TFs) involved in their specification. As indicated, cytotoxic CD4+ T cells can arise from unpolarized Th0, Th1, or Th2 cells in response to IL-2 depending on the context; also, the contributions of the TFs RUNX3, TBET, BLIMP-1, and EOMES to specifying the cytotoxic CD4+ T cell state are also context-dependent, as discussed in the text. (B) Mechanisms that may contribute to activation of cytotoxic CD4+ T cells (red), anti-tumor cytotoxicity effector function (dark blue) including cytokines (light blue), as well as co-stimulatory (orange) or co-inhibitory (green) immune checkpoints are shown.
Figure 1. The ontogeny and regulation of cytotoxic CD4+ T cells in cancer (A) A schematic of known CD4+ T cell functional subtypes, the cytokines that promote their differentiation, and master transcription factors (TFs) involved in their specification. As indicated, cytotoxic CD4+ T cells can arise from unpolarized Th0, Th1, or Th2 cells in response to IL-2 depending on the context; also, the contributions of the TFs RUNX3, TBET, BLIMP-1, and EOMES to specifying the cytotoxic CD4+ T cell state are also context-dependent, as discussed in the text. (B) Mechanisms that may contribute to activation of cytotoxic CD4+ T cells (red), anti-tumor cytotoxicity effector function (dark blue) including cytokines (light blue), as well as co-stimulatory (orange) or co-inhibitory (green) immune checkpoints are shown.CC BY · PubMed Central
Figure 2. Comparison of cytotoxic CD4+ T cell programs in cancer and non-cancer contexts Expression of key transcripts in cytotoxic CD4+ T cells in human and murine cancer, as well as human viral (dengue), murine viral (adenovirus), and human aging. Comparisons were made based on inspection of single-cell transcriptomic data, with the exception of bulk microarray data for murine cancer. Specific references for each dataset, and the platforms used for single-cell sequencing, are indicated. Lighter shading and question marks indicate where findings are inconsistent between datasets (e.g., comparing various human cancers).
Figure 2. Comparison of cytotoxic CD4+ T cell programs in cancer and non-cancer contexts Expression of key transcripts in cytotoxic CD4+ T cells in human and murine cancer, as well as human viral (dengue), murine viral (adenovirus), and human aging. Comparisons were made based on inspection of single-cell transcriptomic data, with the exception of bulk microarray data for murine cancer. Specific references for each dataset, and the platforms used for single-cell sequencing, are indicated. Lighter shading and question marks indicate where findings are inconsistent between datasets (e.g., comparing various human cancers).CC BY · PubMed Central

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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)
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
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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