Branched-chain keto acids promote an immune-suppressive and neurodegenerative microenvironment in leptomeningeal disease.
Mariam Lotfy KhaledYuan RenRonak KundaliaHasan AlhaddadZhihua ChenGerald C WallaceBrittany EverndenOscar E OspinaMacLean HallMin LiuLancia N F DarvilleVictoria IzumiY Ann ChenShari Pilon-ThomasPaul A StewartJohn M KoomenSalvatore A CoralloMichael D JainTimothy J RobinsonFredrick L LockePeter A ForsythInna SmalleyPublished in: bioRxiv : the preprint server for biology (2023)
Leptomeningeal disease (LMD) occurs when tumors seed into the leptomeningeal space and cerebrospinal fluid (CSF), leading to severe neurological deterioration and poor survival outcomes. We utilized comprehensive multi-omics analyses of CSF from patients with lymphoma LMD to demonstrate an immunosuppressive cellular microenvironment and identified dysregulations in proteins and lipids indicating neurodegenerative processes. Strikingly, we found a significant accumulation of toxic branched-chain keto acids (BCKA) in the CSF of patients with LMD. The BCKA accumulation was found to be a pan-cancer occurrence, evident in lymphoma, breast cancer, and melanoma LMD patients. Functionally, BCKA disrupted the viability and function of endogenous T lymphocytes, chimeric antigen receptor (CAR) T cells, neurons, and meningeal cells. Treatment of LMD mice with BCKA-reducing sodium phenylbutyrate significantly improved neurological function, survival outcomes, and efficacy of anti-CD19 CAR T cell therapy. This is the first report of BCKA accumulation in LMD and provides preclinical evidence that targeting these toxic metabolites improves outcomes.
Keyphrases
- cerebrospinal fluid
- cell therapy
- stem cells
- end stage renal disease
- diffuse large b cell lymphoma
- induced apoptosis
- chronic kidney disease
- mesenchymal stem cells
- spinal cord
- peritoneal dialysis
- risk assessment
- papillary thyroid
- type diabetes
- prognostic factors
- high fat diet induced
- squamous cell carcinoma
- cell cycle arrest
- spinal cord injury
- squamous cell
- insulin resistance
- fatty acid
- bone marrow
- cell proliferation
- blood brain barrier
- patient reported
- metabolic syndrome
- glycemic control