作者: Cynthia M Schmidt , Elizabeth Garrett , Harry T Orr
DOI: 10.1016/S0198-8859(97)00097-9
关键词: CD8 、 Human leukocyte antigen 、 Molecular biology 、 Major histocompatibility complex 、 HLA-G 、 Genetically modified mouse 、 Cytotoxic T cell 、 CTL* 、 Biology 、 Transgene 、 Immunology 、 Immunology and Allergy 、 General Medicine
摘要: Abstract Several features of HLA-G’s sequence and expression pattern distinguish HLA-G from its classical counterparts. These features, including limited polymorphism at the maternal-fetal interface, have been used as a basis for suggesting distinct functional role this nonclassical class I HLA molecule. On other hand, published data do demonstrate that has much in common with It associates β2-microglobulin cytosolic peptides, it binds to CD8, presence can inhibit NK-cell-mediated lysis HLA-G-bearing target cells. To develop model which function could be more thoroughly studied, we produced several -expressing transgenic mouse strains. We report here results skin graft experiments show nontransgenic mice reject HLA-G-expressing murine foreign rejection is associated recipient lymphocytes capable specifically lysing In addition, are described recognize “self” Together reported stimulating an HLA-G-restricted CTL response, molecules serve lytic interactions CTLs, involved education lymphocytic repertoire mice.