Bcl-2 transduction protects human endothelial cell synthetic microvessel grafts from allogeneic T cells in vivo

被引:22
作者
Zheng, L
Gibson, TF
Schechner, JS
Pober, JS
Bothwell, ALM
机构
[1] Yale Univ, Sch Med, Immunobiol Sect, New Haven, CT 06520 USA
[2] Yale Univ, Sch Med, Interdept Program Vasc Biol & Transplantat, New Haven, CT 06520 USA
[3] Yale Univ, Sch Med, Dept Dermatol & Pathol, New Haven, CT 06520 USA
关键词
D O I
10.4049/jimmunol.173.5.3020
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
T cell interactions with vascular endothelial cells (EC) are of central importance for immune surveillance of microbes and for pathological processes such as atherosclerosis, allograft rejection, and vasculitis. Animal (especially rodent) models incompletely predict human immune responses, in particular with regard to the immunological functions of EC, and in vitro models may not accurately reflect in vivo findings. In this study, we describe the development of an immunodeficient SCID/bg murine model combining a transplanted human synthetic microvascular bed with adoptive transfer of human T lymphocytes allogeneic to the cells of the graft that more fully recapitulates T cell responses in natural tissues. Using this model, we demonstrate that transduced Bcl-2 protein in the engrafted EC effectively prevents injury even as it enhances T cell graft infiltration and replication.
引用
收藏
页码:3020 / 3026
页数:7
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