Cerebrospinal fluid mtDNA concentrations are increased in multiple sclerosis and were normalized after intervention with autologous hematopoietic stem cell transplantation
•Circulating cell-free mtDNA is released by leukocytes in the inflammatory response.•mtDNA concentrations are elevated in CSF from people with MS.•mtDNA concentrations were normalized in MS patients after intervention with aHSCT. Mitochondrial DNA (mtDNA) is a pro-inflammatory damage-associated mole...
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Veröffentlicht in: | Multiple sclerosis and related disorders 2024-04, Vol.84, p.105482-105482, Article 105482 |
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Zusammenfassung: | •Circulating cell-free mtDNA is released by leukocytes in the inflammatory response.•mtDNA concentrations are elevated in CSF from people with MS.•mtDNA concentrations were normalized in MS patients after intervention with aHSCT.
Mitochondrial DNA (mtDNA) is a pro-inflammatory damage-associated molecular pattern molecule and could be an early indicator for inflammation and disease activity in MS. Autologous hematopoietic stem cell transplantation (aHSCT) is a potent treatment for MS, but its impact on mtDNA levels in cerebrospinal fluid (CSF) remains unexplored.
To verify elevated CSF mtDNA concentrations in MS patients and assess the impact of aHSCT on mtDNA concentrations.
Multiplex droplet digital PCR (ddPCR) was used to quantify mtDNA and nuclear DNA in 182 CSF samples. These samples were collected from 48 MS patients, both pre- and post-aHSCT, over annual follow-ups, and from 32 healthy controls.
CSF ccf-mtDNA levels were higher in patients with MS, correlated to multiple clinical and analytical factors and were normalized after intervention with aHSCT. Differences before aHSCT were observed with regard to MRI-lesions, prior treatment and number of relapses in the last year prior to aHSCT.
Our findings demonstrate elevated CSF mtDNA levels in MS patients, which correlate with disease activity and normalize following aHSCT. These results position mtDNA as a potential biomarker for monitoring inflammatory activity and response to treatment in MS. |
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ISSN: | 2211-0348 2211-0356 2211-0356 |
DOI: | 10.1016/j.msard.2024.105482 |