B细胞耐受性和自身免疫。

T. Tsubata, T. Honjo
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引用次数: 0

摘要

不同的自身抗原诱导B细胞在不同的成熟阶段产生自身耐受性。克隆缺失、克隆能量、受体编辑和成熟阻滞。自身耐受的机制取决于B细胞的成熟阶段和自身抗原的分子性质。B细胞耐受被多种机制所破坏,如抑制共受体缺陷、CD19过表达、T细胞帮助和死亡受体Fas缺陷(CD95)。由于所有这些分子都可以调节由抗原受体或Fas介导的B细胞凋亡,因此B细胞凋亡可能在诱导和维持B细胞耐受中起作用。此外,肠道脂多糖等环境因素也在B细胞耐受性的破坏中发挥作用。
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B cell tolerance and autoimmunity.
Self-tolerance is induced in B cells at various maturational stages by diverse self-antigens B cell tolerance involves multiple mechanisms, ie. clonal deletion, clonal anergy, receptor editing and maturation arrest. The mechanism utilized for self-tolerance depends on both the maturational stage of B cells and the molecular nature of the self-antigens. B cell tolerance is abrogated by various mechanisms such as defects in inhibitory co-receptors, overexpression of CD19, T cell help and defects in the death receptor Fas (CD95). Since all of these molecules regulate B cell apoptosis mediated by either the antigen receptor or Fas, B cell apoptosis may play a role in the induction and maintenance of B cell tolerance. Moreover, environmental factors such as intestinal lipopolysaccharide also play a role in the breakdown of B cell tolerance.
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NCBI genetic resources supporting immunogenetic research. Storage and utilization of HLA genomic data--new approaches to HLA typing. Identifying cytotoxic T cell epitopes from genomic and proteomic information: "The human MHC project.". Bioinformatics: analysis of HLA sequence data. The IMGT/HLA sequence database.
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