Biology and functions of human leukocyte antigen-G in health and sickness

被引:130
作者
LeMaoult, J
Le Discorde, M
Rouas-Freiss, N
Moreau, P
Menier, C
McCluskey, J
Carosella, ED
机构
[1] Hop St Louis, Commissariat Energie Atom, Serv Rech Hematoimmunol, F-75010 Paris, France
[2] Univ Melbourne, Dept Microbiol & Immunol, Parkville, Vic 3052, Australia
来源
TISSUE ANTIGENS | 2003年 / 62卷 / 04期
关键词
cancer; expression regulation; HLA; HLA-G; immune inhibition; pregnancy; tolerance;
D O I
10.1034/j.1399-0039.2003.00143.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In 1998, the first International Conference on human leukocyte antigen-G (I-MA-G) was held in Paris. At that time, HLA-G was still a new HLA class I molecule, few aspects of its immunological functions were known, and its expression by tumors was just being described. In 1998, tools to properly study HLA-G were lacking, especially monoclonal antibodies, and three conclusions were drawn after the congress: (i) animal models were needed, (ii) the biology of HLA-G isoforms had to be confirmed, and (iii) HLA-G expression by tumors required clarification. Five years later, these three issues have been addressed. HLA-G is now gaining pace and is investigated for its immuno-inhibitory functions in the context of multiple pathologies. Eighty five oral presentations were given this year for more than 200 investigators working on HLA-G by speakers from over 20 countries. The success of the 3rd International Conference on HLA-G reflects the interest and tremendous work of the many research teams which, over the years, contributed to the publication of more than 500 peer-review articles. We summarize the key points that were presented and discussed during this meeting.
引用
收藏
页码:273 / 284
页数:12
相关论文
共 70 条
[1]   Selective expression of HLA-G in malignant and premalignant skin specimens in kidney transplant recipients [J].
Aractingi, S ;
Kanitakis, J ;
Euvrard, S ;
Le Danff, C ;
Carosella, ED .
INTERNATIONAL JOURNAL OF CANCER, 2003, 106 (02) :232-235
[2]   Disulfide bond-mediated dimerization of HLA-G on the cell surface [J].
Boyson, JE ;
Erskine, R ;
Whitman, MC ;
Chiu, M ;
Lau, JM ;
Koopman, LA ;
Valter, MM ;
Angelisova, P ;
Horejsi, V ;
Strominger, JL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (25) :16180-16185
[3]  
Bukur J, 2003, CANCER RES, V63, P4107
[4]  
BUKUR J, IN PRESS HUM IMMUNOL
[5]  
CABELLO A, IN PRESS HUM IMMUNOL
[6]   Search for a human homologue of the mouse Ped gene [J].
Cao, W ;
Brenner, CA ;
Alikani, M ;
Cohen, J ;
Warner, CM .
MOLECULAR HUMAN REPRODUCTION, 1999, 5 (06) :541-547
[7]   HLA-G and HLA-E: fundamental and pathophysiological aspects [J].
Carosella, ED ;
Paul, P ;
Moreau, P ;
Rouas-Freiss, N .
IMMUNOLOGY TODAY, 2000, 21 (11) :532-534
[8]   HLA-G: a tolerance molecule from the major histocompatibility complex [J].
Carosella, ED ;
Rouas-Freiss, N ;
Paul, P ;
Dausset, J .
IMMUNOLOGY TODAY, 1999, 20 (02) :60-62
[9]  
CAROSELLA ED, IN PRESS ADV IMMUNOL
[10]   Tolerization of dendritic cells by TS cells:: the crucial role of inhibitory receptors ILT3 and ILT4 [J].
Chang, CC ;
Ciubotariu, R ;
Manavalan, JS ;
Yuan, J ;
Colovai, AI ;
Piazza, F ;
Lederman, S ;
Colonna, M ;
Cortesini, R ;
Dalla-Favera, R ;
Suciu-Foca, N .
NATURE IMMUNOLOGY, 2002, 3 (03) :237-243