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  4. Profiling Immunological Phenotypes in Individuals During the First Year After Traumatic Spinal Cord Injury: A Longitudinal Analysis

Profiling Immunological Phenotypes in Individuals During the First Year After Traumatic Spinal Cord Injury: A Longitudinal Analysis

Journal of Neurotrauma, 2023 · DOI: 10.1089/neu.2022.0500 · Published: December 1, 2023

Spinal Cord InjuryImmunologyBioinformatics

Simple Explanation

This study examines the immune system changes in individuals with spinal cord injury (SCI) during the first year after their injury. It looks at RNA, protein, and cell profiles in blood samples to understand how the immune system changes over time compared to uninjured individuals. The researchers found that there are significant differences in gene expression related to immune function between individuals with SCI and those without, particularly affecting natural killer (NK) cells, monocytes, dendritic cells and T cells. The study also found that the severity of the spinal cord injury (whether it's a complete or incomplete motor injury) correlates with distinct gene expression profiles in the blood, indicating a persistent 'neurogenic' effect on the immune system.

Study Duration
12 Months
Participants
12 individuals with SCI and 23 uninjured individuals
Evidence Level
Not specified

Key Findings

  • 1
    Reduced expression of NK cell genes was observed within the first 6 months post-injury, consistent with reduced frequencies of CD56bright and CD56dim NK cells at 12 months post-injury.
  • 2
    Increased and prolonged expression of genes associated with inflammation (e.g. HMGB1, Toll-like receptor signaling) and expanded frequencies of monocytes were observed over the first 6 months post-injury.
  • 3
    Distinct whole blood gene expression profiles reflecting neurological injury severity were identified, with 2876 differentially expressed genes between motor complete and incomplete SCI, including those related to neutrophils, inflammation, and infection.

Research Summary

This study longitudinally profiled immunological changes in individuals with SCI during the first year post-injury, identifying dynamic molecular and cellular changes using RNA sequencing, flow cytometry, and protein analysis. Key findings include altered expression of genes related to NK cells, monocytes, dendritic cells and T cells, as well as persistent inflammation, and an association between injury severity and gene expression profiles. The identified immunological phenotypes may provide potential targets to reduce inflammation, improve immunity, or serve as candidate biomarkers of injury severity.

Practical Implications

Therapeutic Targets

The identified molecular and cellular changes may provide potential targets for therapeutic interventions aimed at reducing inflammation and improving immunity in individuals with SCI.

Biomarker Development

The study suggests candidate biomarkers of injury severity that could be used to monitor disease progression and treatment response.

Personalized Medicine

Gene expression profiling may be used in a precision medicine approach to inform clinical trials in SCI, testing therapies that target specific immune mediators.

Study Limitations

  • 1
    Challenges of conducting long-term follow up, particularly for geographical reasons.
  • 2
    Inconsistency in sample acquisition at study visits for medical or practical reasons.
  • 3
    The blood samples were comprised of a mixed cell population, so future studies should utilize single-cell RNA-sequencing.

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