The role of B lymphocytes as antigen-presenting cells

被引:110
作者
Chen, Xinjian [1 ]
Jensen, Peter E. [1 ]
机构
[1] Univ Utah, Dept Pathol, Salt Lake City, UT 84112 USA
基金
美国国家卫生研究院;
关键词
B lymphocytes; antigen presentation; HLA-DO; regulatory T cells;
D O I
10.1007/s00005-008-0014-5
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
B lymphocytes are regarded as professional antigen-presenting cells (APCs) despite their primary role in humoral immunity. Over the last two decades, studies designed to define the role of the B cells as APCs have generated discrepant results, showing that B cells are either unnecessary or required for T cell priming and either immunogenic or tolerogenic to T cells. The reasons for these discrepancies are not clear. Here we review mechanisms regulating B cell antigen presentation and the data derived from the major studies conducted by different groups representing each school of thought. In general it is clear that B cells process and present specific and nonspecific antigens differently. The presentation of specific antigen through the B cell antigen receptor occurs with very high efficiency and is associated with B cell activation, resulting in the activation of cognate T cells. In contrast, the presentation of nonspecific antigen by B cells is minimized and dissociated from B cell activation. As a result, B cells inactivate T cells that recognize nonspecific antigenic epitopes presented by B cells, or they induce regulatory T cell differentiation or expansion. These mechanisms serve to ensure effective production of high-affinity antigen-specific antibodies but minimize the production of nonspecific antibodies and autoantibodies.
引用
收藏
页码:77 / 83
页数:7
相关论文
共 71 条
  • [1] Akiba H, 1999, J IMMUNOL, V162, P7058
  • [2] Requirement for phosphoinositide 3-kinase p110δ signaling in B cell antigen receptor-mediated antigen presentation
    Al-Alwan, Monther M.
    Okkenhaug, Klaus
    Vanhaesebroeck, Bart
    Hayflick, Joel S.
    Marshall, Aaron J.
    [J]. JOURNAL OF IMMUNOLOGY, 2007, 178 (04) : 2328 - 2335
  • [3] ASHWELL JD, 1988, J IMMUNOL, V140, P3697
  • [4] Boackle SA, 1998, J IMMUNOL, V161, P6537
  • [5] Early requirement for B cells for development of spontaneous autoimmune thyroiditis in NOD.H-2h4 mice
    Braley-Mullen, H
    Yu, SG
    [J]. JOURNAL OF IMMUNOLOGY, 2000, 165 (12) : 7262 - 7269
  • [6] The actin cytoskeleton is required for the trafficking of the B cell antigen receptor to the late endosomes
    Brown, BK
    Song, WX
    [J]. TRAFFIC, 2001, 2 (06) : 414 - 427
  • [7] Following immunization antigen becomes concentrated in a limited number of APCs including B cells
    Byersdorfer, CA
    DiPaolo, RJ
    Petzold, SJ
    Unanue, ER
    [J]. JOURNAL OF IMMUNOLOGY, 2004, 173 (11) : 6627 - 6634
  • [8] Signal transduction from the B cell antigen-receptor
    Campbell, KS
    [J]. CURRENT OPINION IN IMMUNOLOGY, 1999, 11 (03) : 256 - 264
  • [9] A novel mouse with B cells but lacking serum antibody reveals an antibody-independent role for B cells in murine lupus
    Chan, OTM
    Hannum, LG
    Haberman, AM
    Madaio, MP
    Shlomchik, MJ
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1999, 189 (10) : 1639 - 1647
  • [10] Complete protection from relapsing experimental autoimmune encephalomyelitis induced by syngeneic B cells expressing the autoantigen
    Chen, CC
    Rivera, A
    Dougherty, JP
    Ron, Y
    [J]. BLOOD, 2004, 103 (12) : 4616 - 4618