Herrmann M, Zoller O M, Hagenhofer M, Voll R, Kalden J R
Department for Internal Medicine III, Friedrich-Alexander-University of Erlangen, Germany.
Mol Biol Rep. 1996;23(3-4):265-7. doi: 10.1007/BF00351179.
Analysis of somatic mutations revealed that induction of anti-dsDNA autoantibodies from SLE patients are antigen driven and thus T cell dependent. Since DNA per se has repeatedly been shown not to be immunogenic, various mechanisms leading to the production of anti-dsDNA-antibodies have been discussed including the role of oligonucleosomes. In the present study we demonstrate that the percentage of macrophage engulfing apoptotic cell material was significantly reduced in SLE as compared to control patients. These data suggest that, in contrast to a non-inflammatory clearance of apoptotic cell, phagocytosis of apoptotic cell material may be decreased in SLE patients, possibly leading to a presentation of autoantigens and thus possibly triggering an autoantibody response to nucleoproteins.
体细胞突变分析显示,系统性红斑狼疮(SLE)患者抗双链DNA自身抗体的诱导是抗原驱动的,因此是T细胞依赖性的。由于DNA本身反复被证明没有免疫原性,人们已经讨论了导致抗双链DNA抗体产生的各种机制,包括寡核小体的作用。在本研究中,我们证明与对照患者相比,SLE患者吞噬凋亡细胞物质的巨噬细胞百分比显著降低。这些数据表明,与凋亡细胞的非炎性清除相反,SLE患者对凋亡细胞物质的吞噬作用可能降低,这可能导致自身抗原的呈递,从而可能引发对核蛋白的自身抗体反应。