ABO blood group and related antigens, natural antibodies and transplantation

被引:74
作者
Milland, J. [1 ]
Sandrin, M. S. [1 ]
机构
[1] Univ Melbourne, Dept Surg, Austin Hlth, Melbourne, Vic 3084, Australia
来源
TISSUE ANTIGENS | 2006年 / 68卷 / 06期
关键词
ABO blood group; carbohydrate; natural antibodies; glycosyltransferases; transplantation; xenotransplantation;
D O I
10.1111/j.1399-0039.2006.00721.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The current success rate of transplant surgery and immunosuppression has led to a demand for organs that has outstripped the supply. This has required investigation of alternate strategies. Therefore, allotransplantation across the ABO blood group barrier has commenced, and pig-to-human xenotransplantation is under consideration. The first immunological barrier to both these types of transplantation is the prevention of the antibody-mediated rejection. This rejection is a result of natural preformed antibodies circulating in the serum of the recipient binding to either ABO (for allo) or alpha-galactose (alpha-Gal) (for xeno) antigens expressed on the donor tissue. These antibodies recognise antigens that are, in both cases, carbohydrate molecules with the characteristic feature that the nonreducing terminal carbohydrate is either a Gal or N-acetlygalactosamine residue in an alpha 1,3 linkage. These epitopes are synthesised by closely related members of a single family of glycosyltransferases. This review discusses the carbohydrate antigens, the enzymes involved in their synthesis and the consequences of natural antibodies binding these antigens.
引用
收藏
页码:459 / 466
页数:8
相关论文
共 53 条
[1]   Structure of UDP complex of UDP-galactose:β-galactoside-α-1,3-galactosyltransferase at 1.53-Å resolution reveals a conformational change in the catalytically important C terminus [J].
Boix, E ;
Swaminathan, GJ ;
Zhang, YN ;
Natesh, R ;
Brew, K ;
Acharya, KR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (51) :48608-48614
[2]  
Cohney S, 1999, INT J MOL MED, V3, P199
[3]   Molecular cloning of the gene coding for pig alpha 1->2fucosyltransferase [J].
Cohney, S ;
Mouhtouris, E ;
McKenzie, IFC ;
Sandrin, MS .
IMMUNOGENETICS, 1996, 44 (01) :76-79
[4]  
DIGHIERO G, 1982, J IMMUNOL, V128, P2788
[5]   COMPARTMENTAL ORGANIZATION OF THE GOLGI STACK [J].
DUNPHY, WG ;
ROTHMAN, JE .
CELL, 1985, 42 (01) :13-21
[6]   ONE PERCENT OF HUMAN CIRCULATING B-LYMPHOCYTES ARE CAPABLE OF PRODUCING THE NATURAL ANTI-GAL ANTIBODY [J].
GALILI, U ;
ANARAKI, F ;
THALL, A ;
HILLBLACK, C ;
RADIC, M .
BLOOD, 1993, 82 (08) :2485-2493
[7]   A UNIQUE NATURAL HUMAN-IGG ANTIBODY WITH ANTI-ALPHA-GALACTOSYL SPECIFICITY [J].
GALILI, U ;
RACHMILEWITZ, EA ;
PELEG, A ;
FLECHNER, I .
JOURNAL OF EXPERIMENTAL MEDICINE, 1984, 160 (05) :1519-1531
[8]   Bovine α1,3-galactosyltransferase catalytic domain structure and its relationship with ABO histo-blood group and glycosphingolipid glycosyltransferases [J].
Gastinel, LN ;
Bignon, C ;
Misra, AK ;
Hindsgaul, O ;
Shaper, JH ;
Joziasse, DH .
EMBO JOURNAL, 2001, 20 (04) :638-649
[9]   The elusive NKT cell antigen - Is the search over? [J].
Godfrey, DI ;
Petticci, DG ;
Smyth, MJ .
SCIENCE, 2004, 306 (5702) :1687-+
[10]   Blood group antigens: Molecules seeking a function? [J].
Greenwell, P .
GLYCOCONJUGATE JOURNAL, 1997, 14 (02) :159-173