Abstract
A subset of human follicular helper T cells (TFH) cells expresses CD57 for which no distinct function has been identified. We show that CD57+ TFH cells are universally PD-1hi, but compared to their CD57- PD-1hi counterparts, express little IL-21 or IL-10 among others. Instead, CD57 expression on TFH cells marks cytotoxicity transcriptional signatures that translate into only a weak cytotoxic phenotype. Similarly, circulating PD-1+ CD57+ CD4+ T cells make less cytokine than their CD57- PD-1+ counterparts, but have a prominent cytotoxic phenotype. By analysis of responses to STAT3-dependent cytokines and cells from patients with gain- or loss-of-function STAT3 mutations, we show that CD4+ T cell cytotoxicity is STAT3-dependent. TFH formation also requires STAT3, but paradoxically, once formed, PD-1hi cells become unresponsive to STAT3. These findings suggest that changes in blood and germinal center cytotoxicity might be affected by changes in STAT3 signaling, or modulation of PD-1 by therapy.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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CD57 Antigens / genetics
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CD57 Antigens / immunology*
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Case-Control Studies
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Cell Proliferation
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Cytotoxicity, Immunologic
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Gene Expression Regulation / immunology*
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Humans
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Immunophenotyping
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Interleukin-10 / genetics
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Interleukin-10 / immunology
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Interleukins / genetics
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Interleukins / immunology
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Palatine Tonsil / immunology
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Palatine Tonsil / pathology
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Palatine Tonsil / surgery
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Phenotype
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Primary Cell Culture
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Programmed Cell Death 1 Receptor / genetics
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Programmed Cell Death 1 Receptor / immunology
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STAT3 Transcription Factor / genetics
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STAT3 Transcription Factor / immunology*
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Signal Transduction
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T-Lymphocytes, Cytotoxic / immunology*
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T-Lymphocytes, Cytotoxic / pathology
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T-Lymphocytes, Helper-Inducer / immunology*
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T-Lymphocytes, Helper-Inducer / pathology
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T-Lymphocytes, Regulatory / immunology
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T-Lymphocytes, Regulatory / pathology
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Tonsillectomy
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Tonsillitis / genetics
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Tonsillitis / immunology*
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Tonsillitis / pathology
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Tonsillitis / surgery
Substances
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CD57 Antigens
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IL10 protein, human
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Interleukins
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PDCD1 protein, human
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Programmed Cell Death 1 Receptor
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STAT3 Transcription Factor
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STAT3 protein, human
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Interleukin-10
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interleukin-21