Mouse models with human immunity and their application in biomedical research

被引:43
作者
Zhang, Baojun [1 ,2 ]
Duan, Ziyuan [2 ,3 ]
Zhao, Yong [1 ,2 ]
机构
[1] Chinese Acad Sci, Inst Zool, Transplantat Biol Res Div, State Key Lab Biomembrane & Membrane Biotechnol, Beijing 100101, Peoples R China
[2] China US Joint Res Ctr Life Sci, Beijing, Peoples R China
[3] Chinese Acad Sci, Inst Genet & Dev Biol, Chinese Genom Resources Ctr, Beijing 100101, Peoples R China
关键词
immunodeficient mice; human immune system; biomedicine; transplantation; animal model; PERIPHERAL-BLOOD LYMPHOCYTES; SCID-HU MOUSE; HUMAN T-CELLS; PORCINE ENDOGENOUS RETROVIRUS; VARICELLA-ZOSTER-VIRUS; COMBINED IMMUNODEFICIENCY MICE; DELAYED-TYPE HYPERSENSITIVITY; IN-UTERO TRANSPLANTATION; UMBILICAL-CORD BLOOD; NATURAL-KILLER-CELLS;
D O I
10.1111/j.1582-4934.2008.00347.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Biomedical research in human beings is largely restricted to in vitro studies that lack complexity of a living organism. To overcome this limitation, humanized mouse models are developed based on immunodeficient characteristics of severe combined immunodeficiency ( SCID) or recombination activating gene (Rag)(null) mice, which can accept xenografts. Peripheral constitution of human immunity in SCID or Rag(null) mice has been achieved by transplantation of mature human immune cells, foetal human thymus, bone marrow, liver tissues, lymph nodes or a combination of these, although efficiency needs to be improved. These mouse models with constituted human immunity (defined as humanized mice in the present text) have been widely used to investigate the basic principles of human immunobiology as well as complex pathomechanisms and potential therapies of human diseases. Here, elements of an ideal humanized mouse model are highlighted including genetic and non-genetic modification of recipient mice, transplantation strategies and proposals to improve engraftments. The applications of the humanized mice to study the development and response of human immune cells, human autoimmune diseases, virus infections, transplantation biology and tumour biology are reviewed as well.
引用
收藏
页码:1043 / 1058
页数:16
相关论文
共 179 条
[1]   Ovarian tissue xenografting [J].
Aubard, Y .
EUROPEAN JOURNAL OF OBSTETRICS GYNECOLOGY AND REPRODUCTIVE BIOLOGY, 2003, 108 (01) :14-18
[2]   Disseminated and sustained HIV infection in CD34+ cord blood cell-transplanted Rag2-/-γc-/- mice [J].
Baenziger, Stefan ;
Tussiwand, Roxane ;
Schlaepfer, Erika ;
Mazzucchelli, Luca ;
Heikenwalder, Mathias ;
Kurrer, Michael O. ;
Behnke, Silvia ;
Frey, Joachim ;
Oxenius, Annette ;
Joller, Helen ;
Aguzzi, Adriano ;
Manz, Markus G. ;
Speck, Roberto F. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (43) :15951-15956
[3]   The immediate-early 63 protein of varicella-zoster virus: Analysis of functional domains required for replication in vitro and for T-cell and skin tropism in the SCIDhu model in vivo [J].
Baiker, A ;
Bagowski, C ;
Ito, H ;
Sommer, M ;
Zerboni, L ;
Fabel, K ;
Hay, J ;
Ruyechan, W ;
Arvin, AM .
JOURNAL OF VIROLOGY, 2004, 78 (03) :1181-1194
[4]  
BANKERT RB, 1989, CURR TOP MICROBIOL, V152, P201
[5]   Rejection of human islets and human HLA-A2.1 transgenic mouse islets by alloreactive human lymphocytes in immunodeficient NOD-scid and NOD-Rag1nullPrf1null mice [J].
Banuelos, SJ ;
Shultz, LD ;
Greiner, DL ;
Burzenski, LM ;
Gott, B ;
Lyons, BL ;
Rossini, AA ;
Appel, MC .
CLINICAL IMMUNOLOGY, 2004, 112 (03) :273-283
[6]   SUCCESSFUL ENGRAFTMENT OF HUMAN POSTNATAL THYMUS IN SEVERE COMBINED IMMUNE DEFICIENT (SCID) MICE - DIFFERENTIAL ENGRAFTMENT OF THYMIC COMPONENTS WITH IRRADIATION VERSUS ANTI-ASIALO GM-1 IMMUNOSUPPRESSIVE REGIMENS [J].
BARRY, TS ;
JONES, DM ;
RICHTER, CB ;
HAYNES, BF .
JOURNAL OF EXPERIMENTAL MEDICINE, 1991, 173 (01) :167-180
[7]   ISOLATION OF A CANDIDATE HUMAN HEMATOPOIETIC STEM-CELL POPULATION [J].
BAUM, CM ;
WEISSMAN, IL ;
TSUKAMOTO, AS ;
BUCKLE, AM ;
PEAULT, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (07) :2804-2808
[8]   COMPLEMENT LYTIC ACTIVITY HAS NO ROLE IN THE PATHOGENESIS OF AUTOIMMUNE DIABETES IN NOD MICE [J].
BAXTER, AG ;
COOKE, A .
DIABETES, 1993, 42 (11) :1574-1578
[9]   Dengue fever in humanized NOD/SCID mice [J].
Bente, DA ;
Melkus, MW ;
Garcia, JV ;
Rico-Hesse, R .
JOURNAL OF VIROLOGY, 2005, 79 (21) :13797-13799
[10]  
Bentzien F, 2001, CANCER RES, V61, P7356