Inhibition of cholesteryl ester transfer protein activity in hamsters alters HDL lipid composition

B J Gaynor1, T Sand, R W Clark

  • 1Department of Cardiovascular and Metabolic Diseases, Pfizer, Inc., Groton, CT 06340.

Atherosclerosis
|September 30, 1994
PubMed

Insights

Monoclonal antibody (MAb) 1C4 effectively inhibited cholesteryl ester transfer protein (CETP) activity in hamsters. This inhibition led to increased HDL cholesterol and a favorable shift in HDL lipid composition.

Area of Science:

  • Biochemistry
  • Lipid Metabolism
  • Immunology

Background:

  • Cholesteryl ester transfer protein (CETP) plays a crucial role in lipoprotein metabolism.
  • Understanding CETP's function is vital for developing therapies targeting dyslipidemia.

Purpose of the Study:

  • To investigate the in vivo effects of inhibiting hamster CETP activity using a specific monoclonal antibody (MAb).
  • To analyze the impact of CETP inhibition on HDL lipid composition in hamsters.

Main Methods:

  • Development and screening of monoclonal antibodies against human CETP.
  • Inhibition of hamster CETP activity in vivo using MAb 1C4.
  • Analysis of plasma CETP activity and HDL lipid profiles via ultracentrifugation and FPLC.

Main Results:

  • MAb 1C4 demonstrated significant inhibition of hamster CETP activity (70%-80%) for up to 24 hours post-injection.
  • Inhibition of CETP resulted in a 33% increase in HDL cholesterol and a 31% increase in HDL-CE.
  • A notable 42% decrease in HDL-triglyceride was observed, alongside a redistribution of cholesterol to larger HDL particles.

Conclusions:

  • Monoclonal antibody 1C4 is a potent inhibitor of hamster CETP activity in vivo.
  • Inhibition of CETP leads to a significant improvement in HDL cholesterol levels and composition.
  • Targeting CETP with antibodies represents a promising therapeutic strategy for modulating HDL metabolism.

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