Allorecognition and the alloresponse: clinical implications

被引:103
作者
Afzali, B. [1 ]
Lechler, R. I. [1 ]
Hernandez-Fuentes, M. P. [1 ]
机构
[1] Kings Coll London, Guys Hosp, Dept Nephrol & Transplantat, Immunoregulat Lab, London SE1 9RT, England
来源
TISSUE ANTIGENS | 2007年 / 69卷 / 06期
基金
英国医学研究理事会;
关键词
allorecognition; alloresponses; major histocompatibility complex; minor histocompatibility antigens; rejection; T lymphocytes; transplantation; GRAFT-VERSUS-HOST; MINOR HISTOCOMPATIBILITY ANTIGENS; BONE-MARROW TRANSPLANTATION; CYTOTOXIC T-LYMPHOCYTES; HUMAN NATURAL ANTIBODIES; DENDRITIC CELLS; CLASS-I; ALLOANTIGEN PRESENTATION; COMPLEX ALLOPEPTIDES; INDIRECT RECOGNITION;
D O I
10.1111/j.1399-0039.2007.00834.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The artificial transfer of tissues or cells between genetically diverse individuals elicits an immune response that is adaptive and specific. This response is orchestrated by T lymphocytes that are recognizing, amongst others, major histocompatibility complex (MHC) molecules expressed on the surface of the transferred cells. Three pathways of recognition are described: direct, indirect and semi-direct. The sets of antigens that are recognized in this setting are also discussed, namely, MHC protein products, the MHC class I-related chain (MIC) system, minor histocompatibility antigens and natural killer cell receptor ligands. The end product of the effector responses are hyperacute, acute and chronic rejection. Special circumstances surround the situation of pregnancy and bone marrow transplantation because in the latter, the transferred cells are the ones originating the immune response, not the host. As the understanding of these processes improves, the ability to generate clinically viable immunotherapies will increase.
引用
收藏
页码:545 / 556
页数:12
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