IFNγ-associated immune–metabolic remodeling is linked to serotonin–kynurenine imbalance and cortical vulnerability in lupus-prone mice

Together, these results support an associative framework in which systemic IFNγ levels are linked to cortical metabolic reprogramming and neuronal vulnerability, bridging peripheral immune activation with serotonergic depletion, melatonin loss, axonal injury, and behavioral dysfunction. Translationally, combined blood-based monitoring of IFNγ, NfL, and kynurenine metabolites may represent a candidate biomarker framework for NPSLE. However, validation in independent patient cohorts will be essential, and therapeutic modulation of IDO1/KMO or serotonergic pathways remains an avenue for future investigation.

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Publication Details

Journal
Frontiers in Immunology
Published
2026-03-05
DOI
https://doi.org/10.3389/fimmu.2026.1740039
Primary Topic
Tryptophan and brain disorders
Type
article
Field-Weighted Citation Impact
0.00
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article

IFNγ-associated immune–metabolic remodeling is linked to serotonin–kynurenine imbalance and cortical vulnerability in lupus-prone mice

Jean‐Louis Guéant, Karim Matmat, Emmanuel Darcq, Rosa‐Maria Guéant‐Rodriguez et al.
Frontiers in Immunology
Tryptophan and brain disorders
article

IFNγ-associated immune–metabolic remodeling is linked to serotonin–kynurenine imbalance and cortical vulnerability in lupus-prone mice

Jean‐Louis Guéant, Karim Matmat, Emmanuel Darcq, Rosa‐Maria Guéant‐Rodriguez, Jean-Marc Alberto, Okan Baspinar, Hélène Jeltsch-David
article en

Abstract

Together, these results support an associative framework in which systemic IFNγ levels are linked to cortical metabolic reprogramming and neuronal vulnerability, bridging peripheral immune activation with serotonergic depletion, melatonin loss, axonal injury, and behavioral dysfunction. Translationally, combined blood-based monitoring of IFNγ, NfL, and kynurenine metabolites may represent a candidate biomarker framework for NPSLE. However, validation in independent patient cohorts will be essential, and therapeutic modulation of IDO1/KMO or serotonergic pathways remains an avenue for future investigation.

Frontiers in ImmunologyVol. 17
Constructor University (DE), Cornell University (US), Laboratoire des Sciences de l'Ingénieur, de l'Informatique et de l'Imagerie (FR), Laboratoire National de Référence (MA), Nutrition-Génétique et Exposition aux Risques Environnementaux (FR), Université de Strasbourg (FR), Université de Lorraine (FR)
Openalex Percentile: Top 41%
Tryptophan and brain disorders
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