Lipoprotein apheresis downregulates IL-1α, IL-6 and TNF-α mRNA expression in severe dyslipidaemia

Claudia Stefanutti1, Fabio Mazza1, Daniela Pasqualetti2

  • 1Extracorporeal Therapeutic Techniques Unit, Lipid Clinic and Atherosclerosis Prevention Centre, Department of Molecular Medicine, 'Sapienza' University of Rome, Rome, Italy.

Abstract

Insights

Therapeutic lipoprotein apheresis (LA) significantly reduces pro-inflammatory cytokine mRNA levels, including IL-1α, IL-6, and TNF-α, in patients with dyslipidaemia and coronary artery disease. This suggests LA has an anti-inflammatory effect on arteries.

Area of Science:

  • Cardiovascular Medicine
  • Molecular Biology
  • Immunology

Background:

  • Dyslipidaemias are linked to cardiovascular mortality via inflammatory atherosclerotic plaques.
  • Pro-inflammatory cytokine messenger RNA (mRNA) levels correlate with atherosclerotic disease progression.
  • Therapeutic lipoprotein apheresis (LA) is known to reduce plasma lipids and inflammation.

Purpose of the Study:

  • To evaluate the effects of LA on the expression of mRNA for key pro-inflammatory cytokines.
  • To assess these effects in patients with dyslipidaemia, familial hypercholesterolaemia (HoFH, HeFH), or hyperlipoprotein(a)aemia (hyperLp(a)) and coronary artery disease (CAD).

Main Methods:

  • Ten patients (mean age 47 ± 9.2 years) with hyperLp(a) or genetic dyslipidaemia (HoFH, HeFH) and CAD were enrolled.
  • Messenger RNA (mRNA) expression levels were determined using reverse transcriptase quantitative polymerase chain reaction (RT-qPCR).

Main Results:

  • Lipoprotein apheresis (LA) led to the downregulation of mRNA expression for IL-1α, IL-6, and TNF-α.
  • Reductions were observed after the first LA session and progressively increased by the second session.
  • Maximum decreases were -49% for IL-1α (p < 0.001), -35% for IL-6 (p < 0.001), and -56% for TNF-α (p < 0.001).

Conclusions:

  • Lipoprotein apheresis (LA) suppresses the expression of IL-1α, IL-6, and TNF-α mRNA in patients with dyslipidaemias.
  • This suppression may contribute to the arterial anti-inflammatory effects observed with LA therapy.

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