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Contribution of Toll-like receptor signaling to germinal center antibody responses
被引:56
|作者:
DeFranco, Anthony L.
[1
]
Rookhuizen, Derek C.
[1
,2
]
Hou, Baidong
[1
,3
]
机构:
[1] Univ Calif San Francisco, Dept Microbiol & Immunol, San Francisco, CA 94143 USA
[2] Univ Calif Berkeley, Dept Mol & Cell Biol, Berkeley, CA 94720 USA
[3] Chinese Acad Sci, Inst Biophys, Key Lab Infect & Immun, Beijing 100080, Peoples R China
基金:
美国国家卫生研究院;
中国国家自然科学基金;
关键词:
Toll-like receptor;
B cell;
dendritic cell;
MyD88;
B-CELL RESPONSES;
PLASMA-CELLS;
T-CELLS;
INNATE;
MEMORY;
AUTOIMMUNITY;
SPECIFICITY;
ACTIVATION;
GENERATION;
EVOLUTION;
D O I:
10.1111/j.1600-065X.2012.01115.x
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Toll-like receptors (TLRs) have emerged as one of the most important families of innate immune receptors for initiating inflammation and also for promoting adaptive immune responses. Recent studies have examined the ability of TLRs to promote antibody responses, including T-cell-dependent antibody responses. Initial study suggested that TLR stimulation promotes primarily an extrafollicular antibody response, which rapidly produces moderate affinity antibodies made by short-lived plasma cells. Recent studies, however, have shown that TLRs can also enhance the germinal center response, which produces high affinity class-switched antibody made by long-lived plasma cells. TLR stimulation can increase the magnitude of the latter response and also enhance selection for high affinity IgG. This review summarizes recent advances in understanding the roles of TLRs in B cells and also in other cell types for enhancement of antibody responses, with an emphasis on T-cell-dependent and germinal center antibody responses.
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页码:64 / 72
页数:9
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