Immune Modulation in Xenotransplantation

被引:18
作者
Boksa, Magdalena [1 ]
Zeyland, Joanna [1 ]
Slomski, Ryszard [1 ,2 ]
Lipinski, Daniel [1 ,2 ]
机构
[1] Poznan Univ Life Sci, Dept Biochem & Biotechnol, PL-60632 Poznan, Poland
[2] Polish Acad Sci, Inst Human Genet, PL-60479 Poznan, Poland
关键词
Xenotransplantation; Transgenic pig; Hyperacute rejection; Cytotoxicity; Coagulation; PORCINE ENDOTHELIAL-CELLS; HUMAN NK CELLS; ENDOGENOUS RETROVIRUS PERV; NATURAL-KILLER-CELLS; HYPERACUTE XENOGRAFT REJECTION; TO-BABOON XENOTRANSPLANTATION; POTENTIALLY XENOTIC VIRUSES; DECAY-ACCELERATING FACTOR; HUMAN ALPHA-GALACTOSIDASE; FACTOR PATHWAY INHIBITOR;
D O I
10.1007/s00005-014-0317-7
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The use of animals as donors of tissues and organs for xenotransplantations may help in meeting the increasing demand for organs for human transplantations. Clinical studies indicate that the domestic pig best satisfies the criteria of organ suitability for xenotransplantation. However, the considerable phylogenetic distance between humans and the pig causes tremendous immunological problems after transplantation, thus genetic modifications need to be introduced to the porcine genome, with the aim of reducing xenotransplant immunogenicity. Advances in genetic engineering have facilitated the incorporation of human genes regulating the complement into the porcine genome, knockout of the gene encoding the formation of the Gal antigen (alpha 1,3-galactosyltransferase) or modification of surface proteins in donor cells. The next step is two-fold. Firstly, to inhibit processes of cell-mediated xenograft rejection, involving natural killer cells and macrophages. Secondly, to inhibit rejection caused by the incompatibility of proteins participating in the regulation of the coagulation system, which leads to a disruption of the equilibrium in pro- and anti-coagulant activity. Only a simultaneous incorporation of several gene constructs will make it possible to produce multitransgenic animals whose organs, when transplanted to human recipients, would be resistant to hyperacute and delayed xenograft rejection.
引用
收藏
页码:181 / 192
页数:12
相关论文
共 137 条
[1]   Transgenic pigs for xenotransplantation: selection of promoter sequences for reliable transgene expression [J].
Aigner, Bernhard ;
Klymiuk, Nikolai ;
Wolf, Eckhard .
CURRENT OPINION IN ORGAN TRANSPLANTATION, 2010, 15 (02) :201-206
[2]   Target cell susceptibility to lysis by human natural killer cells is augmented by α(1,3)-galactosyltransferase and reduced by α(1,2)-fucosyltransferase [J].
Artrip, JH ;
Kwiatkowski, P ;
Michler, RE ;
Wang, SF ;
Tugulea, S ;
Ankersmit, J ;
Chisholm, L ;
McKenzie, IFC ;
Sandrin, MS ;
Itescu, S .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (16) :10717-10722
[3]   The SIRP family of receptors and immune regulation [J].
Barclay, AN ;
Brown, MH .
NATURE REVIEWS IMMUNOLOGY, 2006, 6 (06) :457-464
[4]   Clearance of mobilized porcine peripheral blood progenitor cells is delayed by depletion of the pragocytic reticuloendothelial system in baboons [J].
Basker, M ;
Alwayn, IPJ ;
Buhler, L ;
Harper, D ;
Abraham, S ;
Gray, HK ;
DeAngelis, H ;
Awwad, M ;
Down, J ;
Rieben, R ;
White-Scharf, ME ;
Sachs, DH ;
Thall, A ;
Cooper, DKC .
TRANSPLANTATION, 2001, 72 (07) :1278-1285
[5]   First experience with heterotopic thoracic pig-to-baboon cardiac xenotransplantation [J].
Bauer, Andreas ;
Postrach, Johannes ;
Thormann, Michael ;
Blanck, Stefanie ;
Faber, Claudius ;
Wintersperger, Bernd ;
Michel, Sebastian ;
Abicht, Jan-Michael ;
Christ, Frank ;
Schmitz, Christoph ;
Schmoeckel, Michael ;
Reichart, Bruno ;
Brenner, Paolo .
XENOTRANSPLANTATION, 2010, 17 (03) :243-249
[6]   Lack of galactose-α-1,3-galactose expression on porcine endothelial cells prevents complement-induced lysis but not direct xenogeneic NK cytotoxicity [J].
Baumann, BC ;
Forte, P ;
Hawley, RJ ;
Rieben, R ;
Schneider, MKJ ;
Seebach, JD .
JOURNAL OF IMMUNOLOGY, 2004, 172 (10) :6460-6467
[7]   Complement dependent early immunological responses during ex vivo xenoperfusion of hCD46/HLA-E double transgenic pig forelimbs with human blood [J].
Bongoni, Anjan K. ;
Kiermeir, David ;
Jenni, Hansjoerg ;
Baehr, Andrea ;
Ayares, David ;
Klymiuk, Nikolai ;
Wolf, Eckhard ;
Voegelin, Esther ;
Constantinescu, Mihai A. ;
Seebach, Jorg D. ;
Rieben, Robert .
XENOTRANSPLANTATION, 2014, 21 (03) :230-243
[8]   Integrin-associated protein (CD47) and its ligands [J].
Brown, EJ ;
Frazier, WA .
TRENDS IN CELL BIOLOGY, 2001, 11 (03) :130-135
[9]   Thrombin Generation and Platelet Activation in a Xenogenic Lung Perfusion Model Determine Survival of GalTKO.hCD46 Lungs [J].
Burdorf, L. ;
Rybak, E. ;
Riner, A. ;
Zhang, T. ;
Cheng, X. ;
Braileanu, G. ;
Phelps, C. ;
Ayares, D. ;
Azimzadeh, A. M. ;
Pierson, R. N. .
JOURNAL OF HEART AND LUNG TRANSPLANTATION, 2013, 32 (04) :S137-S138
[10]   Increased immunosuppression, not anticoagulation, extends cardiac xenograft survival [J].
Byrne, Guerard W. ;
Davies, William R. ;
Oi, Keiji ;
Rao, Vinay P. ;
Teotia, Sumeet S. ;
Ricci, David ;
Tazelaar, Henry D. ;
Walker, Randall C. ;
Logan, John S. ;
McGregor, Christopher G. A. .
TRANSPLANTATION, 2006, 82 (12) :1787-1791