Mouse models for studies of HLA-G functions in basic science and pre-clinical research

被引:8
|
作者
Anh Thu Nguyen-Lefebvre [1 ]
Ajith, Ashwin [1 ]
Portik-Dobos, Vera [1 ]
Horuzsko, Daniel D. [1 ]
Mulloy, Laura L. [2 ]
Horuzsko, Anatolij [1 ,2 ]
机构
[1] Georgia Regents Univ, Ctr Canc, Mol Oncol & Biomarkers Program, 1140 Laney Walker Blvd, Augusta, GA 30912 USA
[2] Georgia Regents Univ, Dept Med, 1120 15th St, Augusta, GA 30912 USA
关键词
HLA-G; Transgenic mice; Humanized mice; Transplantation; MAJOR HISTOCOMPATIBILITY COMPLEX; CLASS-I MOLECULES; CHORIOCARCINOMA CELL-LINE; DENDRITIC CELLS; HUMANIZED MICE; INHIBITORY RECEPTOR; TRANSGENIC MICE; MYELOMONOCYTIC CELLS; BIOMEDICAL-RESEARCH; T-LYMPHOCYTES;
D O I
10.1016/j.humimm.2016.02.012
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
HLA-G was described originally as a tolerogenic molecule that allows the semiallogeneic fetus to escape from recognition by the maternal immune response. This review will discuss different steps in the study of HLA-G expression and functions in vivo, starting with analyses of expression of the HLA-G gene and its receptors in transgenic mice, and continuing with applications of HLA-G and its receptors in prevention of allograft rejection, transplantation tolerance, and controlling the development of infection. Humanized mouse models have been discussed for developing in vivo studies of HLA-G in physiological and pathological conditions. Collectively, animal models provide an opportunity to evaluate the importance of the interaction between HLA-G and its receptors in terms of its ability to regulate immune responses during maternal-fetal tolerance, survival of allografts, tumor escape mechanisms, and development of infections when both HLA-G and its receptors are expressed. In addition, in vivo studies on HLA-G also offer novel approaches to achieve a reproducible transplantation tolerance and to develop personalized medicine to prevent allograft rejection. (C) 2016 American Society for Histocompatibility and Immunogenetics. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:711 / 719
页数:9
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