Translating Treg Therapy in Humanized Mice

被引:17
|
作者
Hahn, Susanne A. [1 ]
Bellinghausen, Iris [1 ]
Trinschek, Bettina [1 ]
Becker, Christian [1 ]
机构
[1] Johannes Gutenberg Univ Mainz, Univ Med Ctr, Dept Dermatol, D-55122 Mainz, Germany
来源
FRONTIERS IN IMMUNOLOGY | 2015年 / 6卷
关键词
humanized mice; Treg function; therapy; autoimmune disease risk; tolerance; REGULATORY T-CELLS; VERSUS-HOST-DISEASE; CYCLIC ADENOSINE-MONOPHOSPHATE; CHAIN KNOCKOUT MICE; IMMUNE-RESPONSES; DENDRITIC CELLS; MOUSE MODEL; MEDIATED SUPPRESSION; RHEUMATOID-ARTHRITIS; AUTOIMMUNE-DISEASE;
D O I
10.3389/fimmu.2015.00623
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Regulatory T cells (Treg) control immune cell function as well as non-immunological processes. Their far-reaching regulatory activities suggest their functional manipulation as a means to sustainably and causally intervene with the course of diseases. Preclinical tools and strategies are however needed to further test and develop interventional strategies outside the human body. "Humanized" mouse models consisting of mice engrafted with human immune cells and tissues provide new tools to analyze human Treg ontogeny, immunobiology, and therapy. Here, we summarize the current state of humanized mouse models as a means to study human Treg function at the molecular level and to design strategies to harness these cells for therapeutic purposes.
引用
收藏
页数:10
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