Adhesive interactions between human NK cells and porcine endothelial cells

被引:30
作者
Schneider, MKJ [1 ]
Forte, P [1 ]
Seebach, JD [1 ]
机构
[1] Univ Zurich Hosp, Dept Internal Med, Lab Transplantat Immunol, CH-8091 Zurich, Switzerland
关键词
D O I
10.1046/j.1365-3083.2001.00966.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Human natural killer (NK) cells are able to adhere to xenogeneic porcine endothelial cells (EC) and evidence from in vitro studies as well as animal models suggests a potential role fur NK cells in the cellular recognition and damage of porcine xenogeneic tissues. One possible explanation for the observed NK cell-mediated xenogeneic cytotoxicity against porcine EC is the molecular incompatibility between porcine major histocompatibility complex (MHC) class I molecules and MHC-specific inhibitory receptors on human NK cells. In this review we attempt to summarize the current knowledge concerning adhesive interactions between human Mt cells and porcine EC under special considerations of the cross-species receptor-ligand interactions. Methodological differences in assessing adhesion between various studies are reviewed and comparisons to the syngeneic/allogeneic adhesion mechanisms are made. Finally, the therapeutic potential of blocking antibodies and transgenic HLA expression in preventing NK-cell adhesion and xenogeneic cytotoxicity is discussed.
引用
收藏
页码:70 / 75
页数:6
相关论文
共 51 条
[1]  
AlMohanna F, 1997, AM J PATHOL, V151, P111
[2]   Xenogeneic transplantation [J].
Auchincloss, H ;
Sachs, DH .
ANNUAL REVIEW OF IMMUNOLOGY, 1998, 16 :433-470
[3]   Delayed xenograft rejection [J].
Bach, FH ;
Winkler, H ;
Ferran, C ;
Hancock, WW ;
Robson, SC .
IMMUNOLOGY TODAY, 1996, 17 (08) :379-384
[4]   NK cell activation: Distinct stimulatory pathways counterbalancing inhibitory signals [J].
Bakker, ABH ;
Wu, J ;
Phillips, JH ;
Lanier, LL .
HUMAN IMMUNOLOGY, 2000, 61 (01) :18-27
[5]  
Birmele B, 1996, Transpl Immunol, V4, P265, DOI 10.1016/S0966-3274(96)80046-3
[6]  
BIRMELE B, 1994, TRANSPL P, V26, P1150
[7]   Adhesion to target cells is disrupted by the killer cell inhibitory receptor [J].
Burshtyn, DN ;
Shin, J ;
Stebbins, C ;
Long, EO .
CURRENT BIOLOGY, 2000, 10 (13) :777-780
[8]   T cell independence of macrophage and natural killer cell infiltration, cytokine production, and endothelial activation during delayed xenograft rejection [J].
Candinas, D ;
Belliveau, S ;
Koyamada, N ;
Miyatake, T ;
Hechenleitner, P ;
Mark, W ;
Bach, FH ;
Hancock, WW .
TRANSPLANTATION, 1996, 62 (12) :1920-1927
[9]   Comparison between aortic and sinusoidal liver endothelial cells as targets of hyperacute xenogeneic rejection in the pig to human combination [J].
Cattan, P ;
Zhang, BM ;
Braet, F ;
Atia, N ;
Conti, F ;
Conjeaud, H ;
Weill, B ;
Chereau, C ;
Houssin, D ;
Calmus, Y .
TRANSPLANTATION, 1996, 62 (06) :803-810
[10]   Species differences in the expression of major histocompatibility complex class II antigens on coronary artery endothelium - Implications for cell-mediated xenoreactivity [J].
Choo, JK ;
Seebach, JD ;
Nickeleit, V ;
Shimizu, A ;
Lei, H ;
Sachs, DH ;
Madsen, JC .
TRANSPLANTATION, 1997, 64 (09) :1315-1322