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Functional HPV-specific PD-1+ stem-like CD8 T cells in head and neck cancer
An analysis of human papillomavirus (HPV)-specific CD8 T cells in patients with head and neck cancer identifies functional PD-1+TCF-1+CD8 T cells in the tumour with implications for therapeutic vaccination and PD-1 directed immunotherapy.
- Christiane S. Eberhardt
- , Haydn T. Kissick
- & Rafi Ahmed
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An intra-tumoral niche maintains and differentiates stem-like CD8 T cells
The authors examine the immune cell infiltrates of human tumours and provide evidence for a population of CD8 T cells with stem-cell characteristics and proliferative capacity that reside in an antigen-presenting niche within tumours.
- Caroline S. Jansen
- , Nataliya Prokhnevska
- & Haydn Kissick
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Article |
Targeting REGNASE-1 programs long-lived effector T cells for cancer therapy
CRISPR–Cas9 mutagenesis screenings reveal that targeting REGNASE-1 leads to improved therapeutic efficacy of CD8+ T cells against mouse models of cancer, and identify BATF as a key target of REGNASE-1.
- Jun Wei
- , Lingyun Long
- & Hongbo Chi
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Article |
Dynamics and genomic landscape of CD8+ T cells undergoing hepatic priming
CD8+ T cells that are primed by hepatocytes differentiate into dysfunctional T cells, which can be rescued by treatment with IL-2.
- Alexandre P. Bénéchet
- , Giorgia De Simone
- & Matteo Iannacone
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Article |
S-2-hydroxyglutarate regulates CD8+ T-lymphocyte fate
S-2-hydroxyglutarate produced by CD8+ T cells under hypoxic conditions affects locus-specific histone and DNA methylation patterns, which enhances T-cell proliferation, survival and recall responses.
- Petros A. Tyrakis
- , Asis Palazon
- & Randall S. Johnson
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Letter |
T-cell exhaustion, co-stimulation and clinical outcome in autoimmunity and infection
CD8 T-cell exhaustion, although a negative prognostic indicator during persistent infections, is shown to be associated with a good outcome in autoimmune and inflammatory diseases.
- Eoin F. McKinney
- , James C. Lee
- & Kenneth G. C. Smith
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Letter |
Melanomas resist T-cell therapy through inflammation-induced reversible dedifferentiation
A genetically engineered mouse model is used to determine the mechanism of acquired resistance to adoptive therapy with cytotoxic T cells specific for a melanocytic differentiation antigen; tumour necrosis factor (TNF)-α is identified as a crucial factor that causes reversible dedifferentiation of mouse and human melanoma cells.
- Jennifer Landsberg
- , Judith Kohlmeyer
- & Thomas Tüting