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PERIPHERAL DELETION OF SELF-REACTIVE B-CELLS
被引:322
作者:
RUSSELL, DM
DEMBIC, Z
MORAHAN, G
MILLER, JFAP
BURKI, K
NEMAZEE, D
机构:
[1] NATL JEWISH CTR IMMUNOL & RESP MED,DEPT PEDIAT,DIV BASIC SCI,1400 JACKSON ST,DENVER,CO 80206
[2] HOFFMANN LA ROCHE AG,DEPT MOLEC BIOL,CH-4005 BASEL,SWITZERLAND
[3] ROYAL MELBOURNE HOSP,WALTER & ELIZA HALL INST MED RES,PARKVILLE,VIC 3050,AUSTRALIA
[4] ROYAL MELBOURNE HOSP,PARKVILLE,VIC 3050,AUSTRALIA
[5] SANDOZ LTD,DEPT BIOTECHNOL,CH-4002 BASEL,SWITZERLAND
[6] UNIV COLORADO,HLTH SCI CTR,DEPT MICROBIOL & IMMUNOL,DENVER,CO 80262
来源:
关键词:
D O I:
10.1038/354308a0
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
B LYMPHOCYTES are key participants in the immune response because of their specificity, their ability to take up and present antigens to T cells, and their capacity to differentiate into antibody-secreting cells. To limit reactivity to self antigens, autospecific B cells can be functionally inactivated or deleted 1-4. Developing B cells that react with membrane antigens expressed in the bone, marrow are deleted from the peripheral lymphocyte pool 4-6. It is important to ascertain the fate of B cells that recognize membrane autoantigens expressed exclusively on peripheral tissues because B cells in the peripheral lymphoid organs are phenotypically and functionally distinct from bone-marrow B cells 7-9. Here we show that in immunoglobulin-transgenic mice, B cells specific for major histocompatibility complex class I antigen can be deleted if they encounter membrane-bound antigen at a post-bone-marrow stage of development. This deletion may be necessary to prevent organ-specific autoimmunity.
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页码:308 / 311
页数:4
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