Dolphin
Senior Member (Voting Rights)
Neuroscience & Biobehavioral Reviews
Volume 184, May 2026, 106588Immune-cognitive relationships across viral infections: A transnosological systematic review
Anthony Nuber-Champier a, Gautier Bréville b c, Patrice H. Lalive b d, Frédéric Assal b d, Julie A. Péron
a baClinical and Experimental Neuropsychology Laboratory, Department of Psychology and Swiss Centre for Affective Sciences, University of Geneva, SwitzerlandbNeurology Division, Geneva University Hospitals, SwitzerlandcDepartment of Neurology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, USAdFaculty of Medicine, University of Geneva, Switzerland
Received 13 November 2025, Revised 16 January 2026, Accepted 1 February 2026, Available online 2 February 2026, Version of Record 11 February 2026.
What do these dates mean?
Show less
Add to Mendeley
Share
Cite
https://doi.org/10.1016/j.neubiorev.2026.106588Get rights and content
Under a Creative Commons license
Open access
Highlights
- •
Immune signalling dynamically shapes cognitive processes. - •
IL-6, TNF-α, and IFN-γ levels are linked to lower memory and processing speed. - •
Immune balance and intrinsic, extrinsic, trigger factors shape cognition.
Abstract
The emergence of SARS-CoV-2 has renewed interest in the relationship between immunity and cognition.Despite decades of work, the impact of viral exposure, mainly in the field of HIV, herpes and hepatitis infections, on distinct cognitive processes remains unclear, as most studies use global screening tools (e.g., MoCA) in isolation in each infectious context.
This systematic narrative review adopts a transnosological approach, summarizing previously reported immune–cognition relationships across viral infections.
Of 931 studies, 32 met inclusion criteria (N = 25,325) spanning SARS-CoV-2, HIV, herpes, hepatitis, Epstein-Barr virus, and multiple infections.
Reported studies on immuno-cognitive relationships reveal several consistent findings.
Elevated circulating CD14+CD16+ intermediate monocytes correlated with slower processing speed, reduced episodic memory and mental flexibility.
Higher CD4+ T cells were associated with better processing speed, while reduced T cells and B cells levels together with elevated IgG predicted deficits in memory and attention.
Most proinflammatory cytokines (e.g., IL-6, TNF-α, IFN-γ) were associated with impairments in overlapping cognitive domains (e.g., memory), whereas IL-10, an anti-inflammatory cytokine, consistently supported executive and memory performance.