生发中心
体细胞突变
断点群集区域
B细胞受体
B细胞
细胞生物学
抗体
生物
亲和力成熟
B-1电池
等离子体电池
免疫球蛋白D
免疫球蛋白E
细胞分化
CD40
受体
免疫学
免疫系统
基因
T细胞
抗原提呈细胞
遗传学
细胞毒性T细胞
体外
作者
Harry W. Schroeder,Andreas Radbruch,Claudia Berek
出处
期刊:Elsevier eBooks
[Elsevier]
日期:2019-01-01
卷期号:: 107-118.e1
被引量:7
标识
DOI:10.1016/b978-0-7020-6896-6.00007-7
摘要
The establishment of the mature B-cell pool involves a delicate balance that ensures a broad spectrum of specificities and at the same time avoids self-reactivity. B lymphocytes develop from hematopoietic stem cells and their progeny are characterized by a specific B-cell receptor (BCR), which is generated in a somatic rearrangement process. Only when B cells are activated and differentiate into plasma cells will the BCR be secreted in the form of antibodies into the body's fluids. If T-cell help is provided, B cells expressing an immunoglobulin M (IgM) BCR may switch in a germinal center reaction to the Ig classes IgG, IgA, or IgE. In addition, the genes encoding the BCR can be further diversified through hypermutation. Those B cells with a high-affinity receptor are selected to differentiate into long-lived memory B and plasma cells. This B-cell differentiation requires organized immune structures. In inflamed tissues, ectopic lymphoid tissue may develop to support local B-cell differentiation.
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