(Circulation. 2005;112:1054-1062.)
© 2005 American Heart Association, Inc.
Vascular Medicine |
From the Division of Biopharmaceutics, Leiden University, Leiden, the Netherlands (A.D.H., P.d.V., T.J.C.v.B., J.K.); Ludwig Institute for Cancer Research, Brussels Branch, Brussels, Belgium (V.S.); Ludwig Institute for Cancer Research and Cellular Genetics Unit, Université de Louvain, Louvain, Belgium (C.U.); and Ludwig Institute for Cancer Research and Experimental Medicine Unit, Université de Louvain, Louvain, Belgium (J.C.R., J.v.S.).
Correspondence to A.D. Hauer, LACDR, Division of Biopharmaceutics, Gorlaeus Laboratories, Einsteinweg 55, 2333 CC Leiden, PO Box 9502, 2300 RA Leiden, The Netherlands. E-mail A.Hauer{at}LACDR.leidenuniv.nl
Received January 4, 2005; revision received May 4, 2005; accepted May 9, 2005.
Background Interleukin-12 (IL-12) has been identified as a key inducer of a type 1 T-helper cell cytokine pattern, which is thought to contribute to the development of atherosclerosis. We sought to study the role of IL-12 in atherosclerosis by inhibition of IL-12 using a newly developed vaccination technique that fully blocks the action of IL-12.
Methods and Results LDL receptordeficient (LDLr/) mice were vaccinated against IL-12 by 5 intramuscular injections of IL-12PADRE complex in combination with adjuvant oil-in-water emulsion (low dose)/MPL/QS21 every 2 weeks. Two weeks thereafter, atherogenesis was initiated in the carotid artery by perivascular placement of silicone elastomer collars. IL-12 vaccination resulted in the induction of antiIL-12 antibodies that functionally blocked the action of IL-12 as determined in an IL-12 bioassay. Blockade of IL-12 by vaccination of LDLr/ mice resulted in significantly reduced (68.5%; P<0.01) atherogenesis compared with control mice without a change in serum cholesterol levels. IL-12 vaccination also resulted in a significant decrease in intima/media ratios (66.7%; P<0.01) and in the degree of stenosis (57.8%; P<0.01). On IL-12 vaccination, smooth muscle cell and collagen content in the neointima increased 2.8-fold (P<0.01) and 4.2-fold (P<0.01), respectively.
Conclusions Functional blockade of endogenous IL-12 by vaccination resulted in a significant 68.5% reduction in atherogenesis in LDLr/ mice. Vaccination against IL-12 also improved plaque stability, from which we conclude that the blockade of IL-12 by vaccination may be considered a promising new strategy in the treatment of atherosclerosis.
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