Immunological memory: Contribution of memory B cells expressing costimulatory molecules in the resting state

被引:95
作者
Bar-Or, A
Oliveira, EML
Anderson, DE
Krieger, JI
Duddy, M
O'Connor, KC
Hafler, DA
机构
[1] McGill Univ, Montreal Neurol Inst, Neuroimmunol Unit, Montreal, PQ H3A 2B4, Canada
[2] Brigham & Womens Hosp, Ctr Neurol Dis, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Boston, MA 02115 USA
关键词
D O I
10.4049/jimmunol.167.10.5669
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Traditionally, emphasis has been placed on the roles of Th cells in generating and amplifying both cellular and Immoral memory responses. Little is known about the potential contributions of B cell subsets to immunological memory. Resting memory B cells have generally been regarded as poor APC, attributed in part to the relative paucity of costimulatory molecules identified on their surface. We describe a novel subpopulation of human memory B cells that express CD80 in their resting state, are poised to secrete particularly large amounts of class switched Igs, and can efficiently present Ag to and activate T cells. This functionally distinct B cell subset may represent an important mechanism by which quiescent human B cells can initiate and propagate rapid and vigorous immune memory responses. Finally, these studies extend recent observations in the murine system and highlight the phenotypic and functional diversity that exists within the human B cell memory compartment.
引用
收藏
页码:5669 / 5677
页数:9
相关论文
共 55 条
[1]   CTLA4Ig-mediated blockade of T-cell costimulation in patients with psoriasis vulgaris [J].
Abrams, JR ;
Lebwohl, MG ;
Guzzo, CA ;
Jegasothy, BV ;
Goldfarb, MT ;
Goffe, BS ;
Menter, A ;
Lowe, NJ ;
Krueger, G ;
Brown, MJ ;
Weiner, RS ;
Birkhofer, MJ ;
Warner, GL ;
Berry, KK ;
Linsley, PS ;
Krueger, JG ;
Ochs, HD ;
Kelley, SL ;
Kang, SW .
JOURNAL OF CLINICAL INVESTIGATION, 1999, 103 (09) :1243-1252
[2]   Generation of plasma cells from peripheral blood memory B cells: Synergistic effect of interleukin-10 and CD27/CD70 interaction [J].
Agematsu, K ;
Nagumo, H ;
Oguchi, Y ;
Nakazawa, T ;
Fukushima, K ;
Yasui, K ;
Ito, S ;
Kobata, T ;
Morimoto, C ;
Komiyama, A .
BLOOD, 1998, 91 (01) :173-180
[3]   B cell subpopulations separated by CD27 and crucial collaboration of CD27(+) B cells and helper T cells in immunoglobulin production [J].
Agematsu, K ;
Nagumo, H ;
Yang, FC ;
Nakazawa, T ;
Fukushima, K ;
Ito, S ;
Sugita, K ;
Mori, T ;
Kobata, T ;
Morimoto, C ;
Komiyama, A .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1997, 27 (08) :2073-2079
[4]   CD27: a memory B-cell marker [J].
Agematsu, K ;
Hokibara, S ;
Nagumo, H ;
Komiyama, A .
IMMUNOLOGY TODAY, 2000, 21 (05) :204-206
[5]   The B7-CD28/CTLA-4 costimulatory pathways in autoimmune disease of the central nervous system [J].
Anderson, DE ;
Sharpe, AH ;
Hafler, DA .
CURRENT OPINION IN IMMUNOLOGY, 1999, 11 (06) :677-683
[6]   Memory B cells are biased towards terminal differentiation: A strategy that may prevent repertoire freezing [J].
Arpin, C ;
Banchereau, J ;
Liu, YJ .
JOURNAL OF EXPERIMENTAL MEDICINE, 1997, 186 (06) :931-940
[7]   B70 ANTIGEN IS A 2ND LIGAND FOR CTLA-4 AND CD28 [J].
AZUMA, M ;
ITO, D ;
YAGITA, H ;
OKUMURA, K ;
PHILLIPS, JH ;
LANIER, LL ;
SOMOZA, C .
NATURE, 1993, 366 (6450) :76-79
[8]  
Bovia F, 1998, EUR J IMMUNOL, V28, P4418, DOI 10.1002/(SICI)1521-4141(199812)28:12<4418::AID-IMMU4418>3.3.CO
[9]  
2-Z
[10]   A THEORY OF SELF-NONSELF DISCRIMINATION [J].
BRETSCHER, P ;
COHN, M .
SCIENCE, 1970, 169 (3950) :1042-+