Martins, Daniel and Harrison, Neil A. ![]() ![]() |
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Abstract
Beyond their role in immune signalling, cytokines have emerged as key neuromodulators influencing processes including neurotransmitter function, neuronal excitability, synaptic plasticity, neurogenesis, myelination, and cortical sleep-state. These roles are observed in both the healthy brain and during infections when they reorient motivational, cognitive, and emotional responses. Experimental evidence from human and non-human primate immune challenge studies has been pivotal to understanding these effects. By showing that elevated cytokines readily induce transdiagnostic symptoms, including anhedonia, social withdrawal, psychomotor slowing, and cognitive impairment, they have also helped demonstrate that inflammation contributes to the shared neural dysfunction observed across psychiatric and neurological disorders. Cytokines modulate glutamatergic and GABAergic neurotransmission, impair dopaminergic and serotonergic signalling, and regulate homeostatic synaptic scaling, leading to altered network connectivity and behavioural deficits. While research has often focused on single cytokines in isolation, neuroimmune signalling occurs through combinatorial cytokine codes, requiring systems-level approaches to understand their interactive effects. Advances in neuroimaging, molecular neuroscience, and biophysical modelling offer opportunities to link cellular cytokine action with macroscale network dysfunction, enabling mechanistic insights into cytokine-mediated neuromodulation. Clinically, cytokine-targeting therapies hold promise for treating inflammation-driven cognitive and mood disorders, but their long-term impact on neuroplasticity remains uncertain. Future research should characterize immune signatures predictive of neuropsychiatric symptoms, identify cell-type-specific cytokine effects, and integrate multiscale modelling to refine understanding of neuroimmune interactions. Reconceptualising cytokines as fundamental regulators of neural function rather than merely inflammatory mediators is crucial for developing precision medicine to mitigate immune-driven brain dysfunction and improve mental health outcomes.
Item Type: | Article |
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Date Type: | Published Online |
Status: | In Press |
Schools: | Schools > Psychology Research Institutes & Centres > Cardiff University Brain Research Imaging Centre (CUBRIC) |
Publisher: | Elsevier |
ISSN: | 0006-3223 |
Date of First Compliant Deposit: | 21 July 2025 |
Date of Acceptance: | 22 June 2025 |
Last Modified: | 21 Jul 2025 10:42 |
URI: | https://orca.cardiff.ac.uk/id/eprint/179924 |
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