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Proteolytic enzyme activity of blood leukocytes and cerebrospinal fluid in multiple sclerosis

Annals of Neurology
|October 1, 1978
PubMed

Insights

Polymorphonuclear cells release enzymes during multiple sclerosis flares. Elevated neutral proteinase activity in white blood cells and cerebrospinal fluid suggests a role in acute multiple sclerosis pathogenesis.

Area of Science:

  • Neuroimmunology
  • Biochemistry
  • Cell Biology

Background:

  • Polymorphonuclear (PMN) cells are key immune responders.
  • Lysosomal hydrolases, including neutral proteinase, are stored within PMN cells.
  • Multiple sclerosis (MS) is a chronic inflammatory disease of the central nervous system.

Purpose of the Study:

  • To investigate neutral and acid proteinase activity in patients with multiple sclerosis.
  • To explore the relationship between proteinase activity, immune complexes, and disease exacerbation.
  • To assess proteolytic activity in the cerebrospinal fluid of MS patients.

Main Methods:

  • Assaying neutral and acid proteinase activity in circulating white blood cells.
  • Measuring serum immune complex levels.
  • Analyzing cellular fractions of cerebrospinal fluid for neutral proteolytic activity.
  • Monitoring myelin basic protein digestion as an indicator of proteolytic activity.

Main Results:

  • Neutral proteinase activity was increased in circulating white cells during multiple sclerosis exacerbation.
  • Acid proteinase activity was decreased in circulating white cells during multiple sclerosis exacerbation.
  • No correlation was found between proteinase activity and serum immune complex levels.
  • Elevated neutral proteolytic activity was detected in the cerebrospinal fluid of patients with acute multiple sclerosis.

Conclusions:

  • Increased neutral proteinase activity in white blood cells and cerebrospinal fluid may be a biomarker for acute multiple sclerosis.
  • The findings suggest a potential role for PMN-derived neutral proteinases in the pathogenesis of multiple sclerosis, independent of systemic immune complex levels.

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