Sekine Hideharu, Graham Kareem L, Zhao Shenru, Elliott Margaret K, Ruiz Philip, Utz Paul J, Gilkeson Gary S
Department of Medicine, Division of Rheumatology and Immunology, Medical University of South Carolina and the Medical Research Service, Ralph H. Johnson Veterans Affairs Medical Center, Charleston, SC 29425, USA.
J Immunol. 2006 Nov 15;177(10):7423-34. doi: 10.4049/jimmunol.177.10.7423.
We previously described a renal protective effect of factor B deficiency in MRL/lpr mice. Factor B is in the MHC cluster; thus, the deficient mice were H2b, the haplotype on which the knockout was derived, whereas the wild-type littermates were H2k, the H2 of MRL/lpr mice. To determine which protective effects were due to H2 vs factor B deficiency, we derived H2b congenic MRL/lpr mice from the 129/Sv (H2b) strain. Autoantibody profiling using autoantigen microarrays revealed that serum anti-Smith and anti-small nuclear ribonucleoprotein complex autoantibodies, while present in the majority of H2k/k MRL/lpr mice, were absent in the H2b/b MRL/lpr mice. Surprisingly, 70% of MRL/lpr H2b/b mice were found to be serum IgG3 deficient (with few to no IgG3-producing B cells). In addition, H2b/b IgG3-deficient MRL/lpr mice had significantly less proteinuria, decreased glomerular immune complex deposition, and absence of glomerular subepithelial deposits compared with MRL/lpr mice of any H2 type with detectable serum IgG3. Despite these differences, total histopathologic renal scores and survival were similar among the groups. These results indicate that genes encoded within or closely linked to the MHC region regulate autoantigen selection and isotype switching to IgG3 but have minimal effect on end-organ damage or survival in MRL/lpr mice.
我们之前描述了MRL/lpr小鼠中B因子缺乏的肾脏保护作用。B因子位于MHC簇中;因此,缺陷小鼠为H2b,即敲除所源自的单倍型,而野生型同窝小鼠为H2k,即MRL/lpr小鼠的H2。为了确定哪些保护作用是由于H2与B因子缺乏所致,我们从129/Sv(H2b)品系培育出了H2b同源MRL/lpr小鼠。使用自身抗原微阵列进行的自身抗体谱分析显示,血清抗史密斯和抗小核糖核蛋白复合物自身抗体在大多数H2k/k MRL/lpr小鼠中存在,但在H2b/b MRL/lpr小鼠中不存在。令人惊讶的是,发现70%的MRL/lpr H2b/b小鼠血清IgG3缺乏(产生IgG3的B细胞很少或没有)。此外,与任何具有可检测血清IgG3的H2类型的MRL/lpr小鼠相比,H2b/b IgG3缺乏的MRL/lpr小鼠蛋白尿明显减少,肾小球免疫复合物沉积减少,且不存在肾小球上皮下沉积物。尽管存在这些差异,但各组之间的总组织病理学肾脏评分和生存率相似。这些结果表明,MHC区域内编码或与之紧密连锁的基因调节自身抗原选择和向IgG3的同种型转换,但对MRL/lpr小鼠的终末器官损伤或生存影响极小。