High CD6 and low chemokine receptor expression on peripheral blood lymphocytes correlates with MRI gadolinium

Anna Jurewicz1, Krzysztof Zaleski1, Malgorzata Domowicz1

  • 1Department of Neurology, Medical University of Lodz, Lodz, Poland.

Journal of Neuroimmunology
|September 23, 2014
PubMed

Insights

Gadolinium-enhancing lesions in multiple sclerosis (MS) correlate with increased CD6 molecule expression and decreased chemokine receptors on peripheral blood T lymphocytes, suggesting a role in disease progression.

Area of Science:

  • Neuroimmunology
  • Immunogenetics
  • Medical Imaging

Background:

  • Multiple sclerosis (MS) is a chronic inflammatory disease of the central nervous system.
  • Gadolinium-enhancing (Gd(+)) lesions on MRI indicate active inflammation in MS.
  • The role of specific immune cell markers in MS lesion activity requires further elucidation.

Purpose of the Study:

  • To investigate the correlation between Gd(+) lesions in MS patients and the expression of CD6 molecules and chemokine receptors (CCR1, CCR2, CCR3, CCR5) on immune cells.
  • To assess differences in marker expression between MS patients with and without active Gd(+) lesions.

Main Methods:

  • Studied 20 relapsing-remitting MS patients (10 with Gd(+) lesions, 10 without).
  • Measured mRNA and surface expression of CD6 and chemokine receptors using immunostaining and flow cytometry in peripheral blood (PB) and cerebrospinal fluid (CSF).

Main Results:

  • Increased CD6 mRNA and surface expression in PB T lymphocytes of Gd(+) MS patients compared to Gd(-) patients (p<0.01; p<0.05).
  • CD6 mRNA levels correlated positively with the number and size of Gd(+) lesions (r=0.67, r=0.65).
  • Reduced CCR1, CCR2, and CCR3 expression in PB cells of Gd(+) MS patients (p<0.05).
  • Higher co-expression of CD6 with CCR1 and CCR5 in CSF compared to PB T lymphocytes (p<0.05).

Conclusions:

  • Gd(+) lesions in MS are associated with elevated CD6 expression and diminished chemokine receptor expression on peripheral blood T lymphocytes.
  • Co-expression of CD6 with CCR1 and CCR5 may facilitate immune cell transmigration into the CSF, contributing to CNS inflammation in MS.

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