From INSERM U397 (R.E., A.M., J.F.A., F.B.) and INSERM U466 (M.-T.P.,
J.C.T.), Institut L. Bugnard, CHU Rangueil, Toulouse, France.
Correspondence to Francis Bayard, INSERM U397, Institut L. Bugnard, CHU Rangueil, 1 ave Jean Poulhès, 31054 Toulouse Cédex, France. E-mail bayard{at}rangueil.inserm.fr
BackgroundThe cytokines
interleukin 1 (IL-1) and tumor necrosis factor (TNF) are secreted by
the different cell populations of the vascular wall and have been
suggested to promote atherosclerosis.
Methods and ResultsTheir respective roles in fatty-streak
formation in apolipoprotein Edeficient mice were investigated by use
of IL-1 receptor antagonist and TNF binding protein.
Estradiol-17ß was used as a positive control. Blocking TNF seemed to
be active in female animals but not in males. IL-1 receptor
antagonist was as effective as or more effective than
estradiol in both sexes.
ConclusionsIL-1 plays a crucial role in the initial step of the
atherosclerotic process in this animal model, and blocking the activity
of this cytokine should be considered as a therapeutic
possibility.
© 1998 American Heart Association, Inc.
Brief Rapid Communications
Differential Effects of Interleukin-1 Receptor Antagonist and Tumor Necrosis Factor Binding Protein on Fatty-Streak Formation in Apolipoprotein EDeficient Mice
Key Words: atherosclerosis apolipoproteins interleukins tumor necrosis factor
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