HLA-G molecules: from maternal-fetal tolerance to tissue acceptance

被引:266
作者
Carosella, Edgardo D.
Moreau, Philippe
Le Maoult, Joel
Le Discorde, Magali
Dausset, Jean
Rouas-Freiss, Nathalie
机构
[1] Hop St Louis, Inst Univ Hematol,Serv Rech Hematoimmunol, CEA Commissariat Energie Atom, Dept Rech Med,Direct Sci Vivant, F-75015 Paris, France
[2] Fdn Jean Dausset, CEPH, Paris, France
来源
ADVANCES IN IMMUNOLOGY, VOL 81 | 2003年 / 81卷
关键词
D O I
10.1016/S0065-2776(03)81006-4
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Over the past few years, HLA-G, the non-classical HLA class I molecule, has been the center of investigations that have led to the description of its specific structural and functional properties. Although located in the HLA class I region of chromosome six, the HLA-G gene may be distinguished from other HLA class I genes by its low polymorphism and alternative splicing that generates seven HLA-G proteins, whose tissue-distribution is restricted to normal fetal and adult tissues that display a tolerogeneic function toward both innate and acquired immune cells. We review these points, with special emphasis on the role of HLA-G in human pathologies, such as cancer, viral infection, and inflammatory diseases, as well as in organ transplantation.
引用
收藏
页码:199 / +
页数:55
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