HLA Class I Antibodies Provoke Graft Arteriosclerosis in Human Arteries Transplanted into SCID/Beige Mice

被引:30
|
作者
Galvani, S. [1 ,2 ,3 ]
Auge, N. [1 ,2 ,3 ]
Calise, D. [1 ]
Thiers, J. C. [1 ]
Canivet, C. [1 ,2 ,3 ]
Kamar, N. [1 ,2 ,3 ,4 ]
Rostaing, L. [2 ,3 ,4 ]
Abbal, M. [5 ]
Sallusto, F. [4 ]
Salvayre, R. [1 ,2 ,3 ]
Boehler, T. [1 ]
Zou, Y. [6 ]
Stastny, P. [6 ]
Negre-Salvayre, A. [1 ,2 ,3 ]
Thomsen, M. [1 ,2 ,3 ]
机构
[1] CHU Rangueil, INSERM, U858, IFR 31,I2MR,Team 10, F-31054 Toulouse, France
[2] Univ Toulouse 3, F-31062 Toulouse, France
[3] Univ Toulouse, Toulouse, France
[4] CHU Toulouse, Fac Med Toulouse Rangueil, Dept Multiorgan Transplantat, Toulouse, France
[5] CHU Toulouse, Fac Med Toulouse Rangueil, Dept Clin Immunol, Toulouse, France
[6] Univ Texas SW Med Ctr Dallas, Dallas, TX 75390 USA
关键词
Allograft arteriosclerosis; animal models; antibody-mediated rejection; anti-HLA antibodies; chronic allograft rejection; smooth muscle cells; CHRONIC REJECTION; NEOINTIMAL FORMATION; VASCULAR REJECTION; ALLOANTIBODY; PATHOGENESIS; MUTATION; MOUSE;
D O I
10.1111/j.1600-6143.2009.02804.x
中图分类号
R61 [外科手术学];
学科分类号
摘要
Antibodies toward HLA class I and/or MICA are commonly observed in transplanted patients suffering from allograft arteriosclerosis, also called chronic vascular rejection (CVR). The relative importance of cellular versus humoral alloreactivity for CVR is still disputed. We demonstrate that antibodies toward HLA class I provoke lesions typical for CVR in human arteries in vivo in the absence of cellular immunity. To show this, we grafted segments of human mesenteric arteries from 8 deceased organ donors into 36 immunodeficient SCID/beige mice in the infrarenal aortic position. Three mice died postoperatively. The remaining 33 mice received weekly i.v. injections of either a monoclonal antibody toward HLA class I, toward MICA or an irrelevant monoclonal antibody. At sacrifice after 6 weeks, mice receiving the HLA antibody showed a significant neointimal thickening in the grafted artery due to smooth muscle cell (SMC) proliferation while control mice receiving anti-MICA or irrelevant antibody showed little or no thickening. Whereas antibodies toward HLA class I were mitogenic to SMC in vitro, those directed toward MICA did not have any effect. Humoral alloreactivity toward HLA may thus play a causal role for the development of CVR and this opens new possibilities for the treatment of CVR.
引用
收藏
页码:2607 / 2614
页数:8
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