Plasma cell differentiation and survival

被引:160
作者
Tarlinton, David [1 ]
Radbruch, Andreas [2 ,3 ]
Hiepe, Falk [2 ,3 ]
Doerner, Thomas [2 ,3 ]
机构
[1] Royal Melbourne Hosp, Walter & Eliza Hall Inst Med Res, Parkville, Vic 3050, Australia
[2] DRFZ, Berlin, Germany
[3] Charite, D-13353 Berlin, Germany
关键词
D O I
10.1016/j.coi.2008.03.016
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Humoral immunity depends on the regulated production and maintenance of antibody secreting cells during the course of an immune response. Recent insights into the transcriptional regulation of the initiation of plasma cell differentiation have clarified aspects of this process, particularly with respect to the choice between the memory B cell and plasma cell differentiation pathways. It is now possible to specify the conditions favouring these outcomes and to predict where they might occur within the germinal center. Once formed, plasma cell survival is critically dependent on accessing niches that are formed by stomal elements in both normal and inflamed tissues. The apparent homeostasis of plasma cell numbers means that new specificities can persist only at the expense of existing ones, raising questions on how immunological memory is maintained in the face of new immune responses. The answer appears to be through the reduction of the process to a single cell level, thereby introducing an element of stochasticity.
引用
收藏
页码:162 / 169
页数:8
相关论文
共 71 条
[1]   Germinal center dark and light zone organization is mediated by CXCR4 and CXCR5 [J].
Allen, CDC ;
Ansel, KM ;
Low, C ;
Lesley, R ;
Tamamura, H ;
Fujii, N ;
Cyster, JG .
NATURE IMMUNOLOGY, 2004, 5 (09) :943-952
[2]   Germinal-center organization and cellular dynamics [J].
Allen, Christopher D. C. ;
Okada, Takaharu ;
Cyster, Jason G. .
IMMUNITY, 2007, 27 (02) :190-202
[3]   Imaging of germinal center selection events during affinity maturation [J].
Allen, Christopher D. C. ;
Okada, Takaharu ;
Tang, H. Lucy ;
Cyster, Jason G. .
SCIENCE, 2007, 315 (5811) :528-531
[4]   JunD/AP-1 and STAT3 are the major enhancer molecules for high Bcl6 expression in germinal center B cells [J].
Arguni, Eggi ;
Arima, Masafumi ;
Tsuruoka, Nobuhide ;
Sakamoto, Akemi ;
Hatano, Masahiko ;
Tokuhisa, Takeshi .
INTERNATIONAL IMMUNOLOGY, 2006, 18 (07) :1079-1089
[5]   Chemokines and leukocyte traffic [J].
Baggiolini, M .
NATURE, 1998, 392 (6676) :565-568
[6]   Maintenance of serological memory by polyclonal activation of human memory B cells [J].
Bernasconi, NL ;
Traggiai, E ;
Lanzavecchia, A .
SCIENCE, 2002, 298 (5601) :2199-2202
[7]   A role for Toll-like receptors in acquired immunity: up-regulation of TLR9 by BCR triggering in naive B cells and constitutive expression in memory B cells [J].
Bernasconi, NL ;
Onai, N ;
Lanzavecchia, A .
BLOOD, 2003, 101 (11) :4500-4504
[8]   Early appearance of germinal center-derived memory B cells and plasma cells in blood after primary immunization [J].
Blink, EJ ;
Light, A ;
Kallies, A ;
Nutt, SL ;
Hodgkin, PD ;
Tarlinton, DM .
JOURNAL OF EXPERIMENTAL MEDICINE, 2005, 201 (04) :545-554
[9]   IRE1 couples endoplasmic reticulum load to secretory capacity by processing the XBP-1 mRNA [J].
Calfon, M ;
Zeng, HQ ;
Urano, F ;
Till, JH ;
Hubbard, SR ;
Harding, HP ;
Clark, SG ;
Ron, D .
NATURE, 2002, 415 (6867) :92-96
[10]   B cell depletion therapy in systemic lupus erythematosus - Effect on autoantibody and antimicrobial antibody profiles [J].
Cambridge, G. ;
Leandro, M. J. ;
Teodorescu, M. ;
Manson, J. ;
Rahman, A. ;
Isenberg, D. A. ;
Edwards, J. C. .
ARTHRITIS AND RHEUMATISM, 2006, 54 (11) :3612-3622