Blood Serum Cytokines in Patients with Subacute Spinal Cord Injury: A Pilot Study to Search for Biomarkers of Injury Severity.
Sergei OgurcovIliya ShulmanEkaterina GaraninaDavran SabirovIrina BaichurinaMaxim KuznetcovGalina MasgutovaAlexander KostennikovAlbert Anatolyevich RizvanovVictoria JamesYana Olegovna MukhamedshinaPublished in: Brain sciences (2021)
Background. Despite considerable interest in the search for a spinal cord injury (SCI) therapy, there is a critical need to develop a panel of diagnostic biomarkers to determine injury severity. In this regard, there is a requirement for continuing research into the fundamental processes of neuroinflammatory and autoimmune reactions in SCI, identifying changes in the expression of cytokines. Methods. In this pilot study, an extended multiplex analysis of the cytokine profiles in the serum of patients at 2 weeks post-SCI (n = 28) was carried out, together with an additional assessment of neuron-specific enolase (NSE) and vascular endothelial growth factor (VEGF) levels by enzyme-linked immunosorbent assay. A total of 16 uninjured subjects were enrolled as controls. Results. The data obtained showed a large elevation of IFNγ (>52 fold), CCL27 (>13 fold), and CCL26 (>8 fold) 2 weeks after SCI. The levels of cytokines CXCL5, CCL11, CXCL11, IL10, TNFα, and MIF were different between patients with baseline American Spinal Injury Association Impairment Scale (AIS) grades of A or B, whilst IL2 (>2 fold) and MIP-3a (>6 fold) were significantly expressed in the cervical and thoracic regions. There was a trend towards increasing levels of NSE. However, the difference in NSE was lost when the patient set was segregated based on AIS group. Conclusions. Our pilot research demonstrates that serum concentrations of cytokines can be used as an affordable and rapid detection tool to accurately stratify SCI severity in patients.
Keyphrases
- spinal cord injury
- vascular endothelial growth factor
- spinal cord
- neuropathic pain
- liver injury
- liver fibrosis
- high throughput
- poor prognosis
- endothelial cells
- ejection fraction
- loop mediated isothermal amplification
- newly diagnosed
- drug induced
- end stage renal disease
- rheumatoid arthritis
- randomized controlled trial
- immune response
- multiple sclerosis
- patient reported outcomes
- machine learning
- clinical trial
- dendritic cells
- study protocol
- big data
- bone marrow
- mesenchymal stem cells