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BCR signaling in germinal center B cell selection
被引:1
作者:
Inoue, Takeshi
[1
]
Baba, Yoshihiro
[2
]
Kurosaki, Tomohiro
[3
,4
,5
]
机构:
[1] Univ Tokyo, Pandem Preparedness Infect & Adv Res Ctr UTOPIA, Dept Mol Syst Immunol, Tokyo, Japan
[2] Kyushu Univ, Med Inst Bioregulat, Div Immunol & Genome Biol, Fukuoka, Japan
[3] Osaka Univ, World Premier Int WPI Immunol Frontier Res Ctr, Lab Lymphocyte Differentiat, Osaka, Japan
[4] Osaka Univ, Ctr Infect Dis Educ & Res, Osaka, Japan
[5] RIKEN Ctr Integrat Med Sci IMS, Lab Lymphocyte Differentiat, Yokohama, Kanagawa, Japan
基金:
日本学术振兴会;
关键词:
FOLLICULAR HELPER-CELL;
TRANSCRIPTION FACTOR;
DARK ZONE;
SOLUBLE-ANTIGEN;
PI3;
KINASE;
RECEPTOR;
DIFFERENTIATION;
ENTRY;
STIM1;
IMMUNOGLOBULIN;
D O I:
10.1016/j.it.2024.07.005
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
When mature B cells are activated by antigens, the selection of these activated cells takes place particularly during T cell-dependent immune responses in which an improved antibody repertoire is generated through somatic hypermutation germinal centers (GCs). In this process the importance of antigen presentation by GC B cells, and subsequent T follicular helper (Tfh) cell help in positive selection of GC B cells, has been well appreciated. By contrast, the role of B cell receptor (BCR) signaling per se remains unclear. Strong experimental support for involvement of BCR signaling in GC B cell selection has now been provided. Interestingly, these studies suggest that several checkpoints operating through BCR ensure affinity i nity maturation.
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页码:693 / 704
页数:12
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