# Computational modeling-directed combination treatment with etanercept and mifepristone mitigates neuroinflammation in a mouse model of Gulf War Illness

**Authors:** Kimberly A. Kelly, Christopher M. Felton, Brenda K. Billig, Ali A. Yilmaz, James P. O’Callaghan, Travis J. A. Craddock, Gordon Broderick, Nancy Klimas, Lindsay T. Michalovicz

PMC · DOI: 10.1371/journal.pone.0324577 · PLOS One · 2026-03-17

## TL;DR

A combination of etanercept and mifepristone reduces neuroinflammation in a mouse model of Gulf War Illness, offering a potential new treatment strategy.

## Contribution

A novel combination therapy for Gulf War Illness, identified through computational modeling and validated in a mouse model.

## Key findings

- The drug combination significantly alleviates neuroinflammation in a Gulf War Illness mouse model.
- Computational modeling successfully predicted effective treatment strategies for Gulf War Illness.
- Combining anti-inflammatory and anti-glucocorticoid treatments shows promise for treating Gulf War Illness.

## Abstract

Gulf War Illness is a chronic multi-symptom disorder experienced by over 30% of veterans from the 1990–1991 Gulf War and is increasingly recognized to be driven by underlying persistent neuroinflammation resulting from chemical and physiological exposures experienced during deployment. Despite significant advances in identifying Gulf War-relevant exposures and underlying pathobiology, effective treatment strategies for Gulf War Illness are still largely lacking. Many studies that have evaluated potential therapies for Gulf War Illness have primarily focused on a single treatment. However, through a mechanistically informed computational evaluation of blood biomarkers and gene expression in veterans with Gulf War Illness, we identified that a combination of anti-inflammatory and anti-glucocorticoid treatment may prove effective in treating Gulf War Illness. Here, we have evaluated combined treatment with the anti-TNFα drug, etanercept, and anti-glucocorticoid, mifepristone, in an established long-term mouse model of Gulf War Illness of combined physiological stress and nerve agent exposure. Supporting results from the computational modeling of this treatment, we found that this drug combination significantly alleviates the underlying neuroinflammation associated with Gulf War Illness. The fusion of computational and in vivo preclinical treatment evaluation may provide a highly useful and translationally relevant means by which to identify successful treatment paradigms for Gulf War Illness.

## Linked entities

- **Chemicals:** mifepristone (PubChem CID 4196)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Lif (leukemia inhibitory factor) [NCBI Gene 16878], Ache (acetylcholinesterase) [NCBI Gene 11423], Il1b (interleukin 1 beta) [NCBI Gene 16176] {aka IL-1beta, Il-1b}, Tnf (tumor necrosis factor) [NCBI Gene 21926] {aka DIF, TNF-a, TNF-alpha, TNFSF2, TNFalpha, Tnfa}, Osm (oncostatin M) [NCBI Gene 18413] {aka OncoM}, Ccl2 (C-C motif chemokine ligand 2) [NCBI Gene 20296] {aka HC11, JE, MCAF, MCP-1, MCP1, SMC-CF}, Gfap (glial fibrillary acidic protein) [NCBI Gene 14580], Il6 (interleukin 6) [NCBI Gene 16193] {aka Il-6}, Gapdh (glyceraldehyde-3-phosphate dehydrogenase) [NCBI Gene 14433] {aka Gapd}, Nr3c1 (nuclear receptor subfamily 3, group C, member 1) [NCBI Gene 14815] {aka GR, Grl-1, Grl1}
- **Diseases:** miosis (MESH:D015877), neuroimmune dysregulation (MESH:D021081), War (MESH:D000067398), neuroimmune dysfunction (MESH:D006331), neuro-based illness and disease (MESH:D004194), brain injuries (MESH:D001930), neuroinflammation (MESH:D000090862), cognitive impairments (MESH:D003072), neurotoxic (MESH:D020258), pain (MESH:D010146), toxicity (MESH:D064420), neurological diseases (MESH:D020271), endocrine disruption (MESH:D004700), gastrointestinal upset (MESH:D005767), immune dysregulation (OMIM:614878), GWI (MESH:D018923), burn (MESH:D002056), inflammatory (MESH:D007249), emesis (MESH:D014839)
- **Chemicals:** CORT DFP (-), mifepristone (MESH:D015735), pyrethroid (MESH:D011722), curcumin (MESH:D003474), pyridostigmine bromide (MESH:D011729), EtOH (MESH:D000431), sesame oil (MESH:D012715), pentobarbital (MESH:D010424), sarin (MESH:D012524), progesterone (MESH:D011374), permethrin (MESH:D026023), organophosphate (MESH:D010755), CO2 (MESH:D002245), DFP (MESH:D007531), LPS (MESH:D008070), propranolol (MESH:D011433), LNFPIII (MESH:C434666), CORT (MESH:D003345), melatonin (MESH:D008550), Saline (MESH:D012965), cyclosarin nerve agents (MESH:C053914), water (MESH:D014867)
- **Species:** Rodentia (rodent, order) [taxon 9989], Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12994794/full.md

## References

48 references — full list in the complete paper: https://tomesphere.com/paper/PMC12994794/full.md

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Source: https://tomesphere.com/paper/PMC12994794