Local and Systemic Humoral Response to Autologous Lineage-Negative Cells Intrathecal Administration in ALS Patients.
Bartłomiej BaumertAnna SobuśMonika Gołąb-JanowskaZofia LitwińskaEdyta PaczkowskaKarolina ŁuczkowskaAlicja ZawiślakSławomir MilczarekBogumiła OsękowskaAgnieszka MellerKarolina Machowska-SempruchAgnieszka WełnickaKrzysztof SafranowPrzemysław NowackiBogusław MachalińskiPublished in: International journal of molecular sciences (2020)
Amyotrophic lateral sclerosis (ALS) remains a fatal disease with limited therapeutic options. Signaling via neurotrophins (NTs), neuroinflammation, and certain micro-RNAs are believed to play essential role in ALS pathogenesis. Lineage-negative stem/progenitor cells (Lin-) were obtained from bone marrow of 18 ALS patients and administered intrathecally. Clinical assessment was performed using ALS Functional Rating Scale (FRSr) and Norris scale. Protein concentrations were measured in plasma and cerebrospinal fluid (CSF) by multiplex fluorescent bead-based immunoassay. Gene expression in nucleated blood cells was assessed using gene microarray technique. Finally, miRNA expression was analyzed using qPCR in CSF and plasma samples. We observed a significant decrease of C-reactive protein (CRP) concentration in plasma on the seventh day from the application of cells. Gene array results revealed decreased expression of gene sets responsible for neutrophil activation. Further analysis revealed moderate negative correlation between CRP level in CSF and clinical outcome. Brain-derived neurotrophic factor (BDNF) concentrations in both plasma and CSF significantly correlated with the favorable clinical outcome. On a micro-RNA level, we observed significant increase of miR-16-5p expression one week after transplantation in both body fluids and significant increase of miR-206 expression in plasma. Administration of Lin- cells may decrease inflammatory response and prevent neurodegeneration. However, these issues require further investigations.
Keyphrases
- amyotrophic lateral sclerosis
- induced apoptosis
- poor prognosis
- gene expression
- cell cycle arrest
- bone marrow
- cerebrospinal fluid
- inflammatory response
- end stage renal disease
- long non coding rna
- chronic kidney disease
- single cell
- newly diagnosed
- immune response
- genome wide
- traumatic brain injury
- prognostic factors
- endoplasmic reticulum stress
- randomized controlled trial
- high throughput
- cell proliferation
- copy number
- clinical trial
- small molecule
- quantum dots
- toll like receptor
- lps induced
- blood brain barrier
- mass spectrometry
- cord blood
- pi k akt
- real time pcr