Unique site of IgG2a and rheumatoid factor production in MRL/lpr mice

被引:19
作者
Jacobson, BA
Rothstein, TL
MarshakRothstein, A
机构
[1] BOSTON UNIV,SCH MED,DEPT MICROBIOL,BOSTON,MA 02118
[2] GENET INST INC,CAMBRIDGE,MA 02140
[3] BOSTON UNIV,SCH MED,DEPT MED,BOSTON,MA 02118
关键词
D O I
10.1111/j.1600-065X.1997.tb00962.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
MRL/lpr (Fas-deficient) mice develop an autoimmune syndrome associated. with excessive production of autoantibodies. A significant portion of these autoantibodies are IgG2a molecules specific for many of the autoantigens recognized by the sera of patients with systemic lupus erythematosus. In addition, MRL/lpr mice make exceedingly high titers of IgG or IgA rheumatoid factors (RF) specific for autologous IgG2a, The microenvironment of the IgG2a-producing B cells as well as the prototypic RF autoantibodies was determined by a combination of immunohistochemical and in situ hybridization techniques. In contrast to the antibody-producing cells present in mice responding to conventional foreign antigens, both IgG2a(+) and RF+ B cells were found to be densely clustered in the T-cell-rich inner periarteriolar lymphatic sheath of the spleen. These results suggest that conventional antibody and autoantibody production in MRL/lpr mice may be mechanistically distinct processes.
引用
收藏
页码:103 / 110
页数:8
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