B cell memory: building two walls of protection against pathogens

被引:424
作者
Akkaya, Munir [1 ]
Kwak, Kihyuck [1 ]
Pierce, Susan K. [1 ]
机构
[1] NIAID, Immunogenet Lab, NIH, Rockville, MD 20852 USA
关键词
GERMINAL CENTER B; LIVED PLASMA-CELLS; SUBCAPSULAR SINUS MACROPHAGES; YELLOW-FEVER VACCINE; TRANSCRIPTION FACTOR; ANTIBODY-RESPONSE; LYMPH-NODES; ANTIGEN; RECEPTOR; CENTERS;
D O I
10.1038/s41577-019-0244-2
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Surviving a single infection often results in lifelong immunity to the infecting pathogen. Such protection is mediated, in large part, by two main B cell memory 'walls' - namely, long-lived plasma cells and memory B cells. The cellular and molecular processes that drive the production of long-lived plasma cells and memory B cells are subjects of intensive research and have important implications for global health. Indeed, although nearly all vaccines in use today depend on their ability to induce B cell memory, we have not yet succeeded in developing vaccines for some of the world's most deadly diseases, including AIDS and malaria. Here, we describe the two-phase process by which antigen drives the generation of long-lived plasma cells and memory B cells and highlight the challenges for successful vaccine development in each phase. The authors discuss the formation of two main 'walls' of B cell memory to protect against pathogen reinfection. The first wall comprises high-affinity antibodies produced by long-lived plasma cells, while the second wall is formed by memory B cells.
引用
收藏
页码:229 / 238
页数:10
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