Year: 2026
Type: article
Abstract: ABSTRACT Wang et al. identify CXCL10 high TNFα high Ki67 + microglia as drivers of CD8 + T cell recruitment during experimental cerebral malaria (ECM). We propose a conservative reframing: rather than asserting a fully validated new taxonomy, CXCL10 high microglia should be considered a candidate “neuroimmune endotype” whose translational relevance requires clearly prespecified and testable validation in human disease. Priority validation steps include single‐nucleus and spatial transcriptomics of human postmortem tissue, paired plasma/CSF biomarker correlation, and mechanistic assays of microglial antigen presentation. We caution against strong therapeutic inferences from ECM alone; translational work should first establish reproducible human microglial signatures and clinical correlations before precision‐targeted interventions are proposed.
Source: CNS Neuroscience & Therapeutics
DOI: 10.1002/cns.70742
Institutions: Burapha University, Naresuan University
Language: English
Subfield: Neurology
Field: Neuroscience
Domain: Life Sciences
Open Access status: gold
Estimated APC paid: $4,140
OpenAlex ID: W7120190370
