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- W2069322489 endingPage "693" @default.
- W2069322489 startingPage "681" @default.
- W2069322489 abstract "Multiple mechanisms underlie the surprising willingness of mothers to tolerate genetically different fetal tissues during pregnancy. Chief among these is the choice of HLA-G, a gene with few alleles, rather than the highly polymorphic HLA-A and -B genes, for expression by the placental cells that interface directly with maternal blood and tissues. Novel aspects of this major histocompatibility complex class Ib gene include alternative splicing to permit production of membrane and soluble isoforms, deletions that dampen responses to interferons, and a shortened cytoplasmic tail that affects expression at the cell surface. Placental cells migrating into the maternal uterus synthesize both membrane and soluble isoforms, which interact with inhibitory receptors on leukocytes such as ILT2 and ILT4. Cytotoxic T lymphocytes either die or reduce production of one of their major coreceptor/activator cell surface molecules, CD8; natural killer cells are immobilized and mononuclear phagocytes are programmed into suppressive modes characterized by high production of anti-inflammatory cytokines. The idea that placental HLA-G proteins facilitate semiallogeneic pregnancy by inhibiting maternal immune responses to foreign (paternal) antigens via these actions on immune cells is now well established, and the postulate that the recombinant counterparts of these proteins may be used as powerful tools for preventing immune rejection of transplanted organs is gaining in popularity." @default.
- W2069322489 created "2016-06-24" @default.
- W2069322489 creator A5011509778 @default.
- W2069322489 creator A5022531995 @default.
- W2069322489 creator A5032262446 @default.
- W2069322489 creator A5067673155 @default.
- W2069322489 date "2005-05-01" @default.
- W2069322489 modified "2023-10-16" @default.
- W2069322489 title "HLA‐G and immune tolerance in pregnancy" @default.
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