The cellular mechanism by which complementary Id+ and anti-Id antibodies communicate: T cells integrated into idiotypic regulation

被引:20
作者
Jacobsen, Johanne T. [1 ,2 ]
Lunde, Elin [1 ,2 ]
Sundvold-Gjerstad, Vibeke [3 ]
Munthe, Ludvig A. [1 ,2 ]
Bogen, Bjarne [1 ,2 ]
机构
[1] Univ Oslo, Inst Immunol, Ctr Immune Regulat, N-0027 Oslo, Norway
[2] Oslo Univ Hosp Norway, Rigshosp, Oslo, Norway
[3] Univ Oslo, Inst Basic Med Sci, Dept Anat, N-0027 Oslo, Norway
关键词
immune regulation; idiotypic network; immunoglobulins; B cells; T cells; B- to T-cell collaboration; IMMUNOGLOBULIN VARIABLE-REGION; 3RD HYPERVARIABLE REGION; B-LYMPHOMA CELLS; COMPLEX CLASS-II; MYELOMA PROTEIN; MONOCLONAL-ANTIBODIES; IN-VIVO; ENDOGENOUS IMMUNOGLOBULIN; ANTIIDIOTYPIC ANTIBODIES; SURFACE-IMMUNOGLOBULIN;
D O I
10.1038/icb.2009.118
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The V region antigenic determinants (idiotopes (Ids)) of antibodies (Abs) have been suggested to be involved in regulating the immune system. Certain diseases such as diabetes mellitus have recently been associated with a disequilibrium between Id(+) and anti-Id Abs. However, it is unknown how Abs carrying complementary idiotypes (that is, Id+ and anti-Id Abs) regulate each other at the level of B and T cells. In this study, we show that B lymphoma cells genetically equipped with anti-Id BCR V regions receive a signal when exposed to Id(+)Ig. Moreover, they become x10(4) more efficient at presenting exogenous Id(+) Ab to CD4(+) T cells in vitro. Activated Id-specific T cells in turn regulated the Id-specific B lymphoma cells. Similar results were obtained in vivo in a surrogate model in which an Id-peptide was incorporated genetically into the C-region of a recombinant Ab that targeted IgD on B cells. The findings suggest that conventional T-B collaboration can explain communication between complementary Id(+) and anti-Id Ab at the cellular level. A model is suggested that integrates present and previous data on B-cell regulation by Id-specific T cells. Immunology and Cell Biology (2010) 88, 515-522; doi: 10.1038/icb.2009.118; published online 12 January 2010
引用
收藏
页码:515 / 522
页数:8
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