Journal of immunology research · 2026
Regulatory Effects of CD14+CD16++Slan+ Monocytes on Classical Monocytes and T Lymphocytes in Response to Inflammatory and Phagocytic Stimuli.
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Anacona Cristian A, Álvarez Karen, Vásquez Gloria, Rojas Mauricio
Аннотация
BACKGROUND: CD14+CD16++6-sulfo LacNAc (Slan)+ monocytes represent a specialized nonclassical subset with reported pro-inflammatory and regulatory features. However, their capacity to modulate classical monocytes and T lymphocytes under apoptotic and inflammatory conditions remains incompletely defined.
METHODS: We employed a coculture reconstitution model using flow cytometry-sorted CD14+CD16++Slan+ monocytes and CD14++CD16-Slan- classical monocytes at defined ratios. Cultures were stimulated with lipopolysaccharide (LPS) or K562-derived apoptotic bodies (ABs). Monocyte surface marker expression was evaluated by flow cytometry, and cytokine concentrations were quantified using multiplex bead-based assays. The impact of Slan+ monocytes on CD3+ T cell proliferation and cytokine production was assessed following monocyte-T cell coculture.
RESULTS: CD14+CD16++Slan+ monocytes exhibited enhanced uptake of ABs and distinct phenotypic modulation upon stimulation. Increasing proportions of Slan+ cells induced higher HLA-DR and CCR5 expression on classical monocytes. LPS stimulation promoted TNF, IL-12, IL-6, and CCL2 production, whereas AB exposure favored IL-10 and IL-17 accumulation. In coculture assays, Slan+ monocytes reduced CD4+ and CD8+ T cell proliferation and altered T cell cytokine profiles in a stimulus-dependent manner.
CONCLUSION: CD14+CD16++Slan+ monocytes exert a dose- and context-dependent modulatory effect on classical monocytes and T lymphocytes in vitro, displaying both inflammatory and regulatory properties depending on the stimulus. These findings highlight their functional plasticity within the human monocyte compartment.
METHODS: We employed a coculture reconstitution model using flow cytometry-sorted CD14+CD16++Slan+ monocytes and CD14++CD16-Slan- classical monocytes at defined ratios. Cultures were stimulated with lipopolysaccharide (LPS) or K562-derived apoptotic bodies (ABs). Monocyte surface marker expression was evaluated by flow cytometry, and cytokine concentrations were quantified using multiplex bead-based assays. The impact of Slan+ monocytes on CD3+ T cell proliferation and cytokine production was assessed following monocyte-T cell coculture.
RESULTS: CD14+CD16++Slan+ monocytes exhibited enhanced uptake of ABs and distinct phenotypic modulation upon stimulation. Increasing proportions of Slan+ cells induced higher HLA-DR and CCR5 expression on classical monocytes. LPS stimulation promoted TNF, IL-12, IL-6, and CCL2 production, whereas AB exposure favored IL-10 and IL-17 accumulation. In coculture assays, Slan+ monocytes reduced CD4+ and CD8+ T cell proliferation and altered T cell cytokine profiles in a stimulus-dependent manner.
CONCLUSION: CD14+CD16++Slan+ monocytes exert a dose- and context-dependent modulatory effect on classical monocytes and T lymphocytes in vitro, displaying both inflammatory and regulatory properties depending on the stimulus. These findings highlight their functional plasticity within the human monocyte compartment.