Datta S K, Mohan C, Desai-Mehta A
Department of Medicine, Northwestern University Medical School, Chicago, Ill. 60611-3008, USA.
Immunol Res. 1995;14(2):132-47. doi: 10.1007/BF02918173.
A major step towards understanding the basic mechanism of systemic lupus erythematosus (SLE), the prototypic autoimmune disease that develops spontaneously, has been the identification of nucleosomes as a primary immunogen in this disease. The production of pathogenic autoantibodies in SLE results from an MHC class-II-restricted, cognate interaction between select populations of T helper cells and B cells that are specific for nucleosomal components. These observations pave the way for specific immunotherapy that blocks this pathogenic T and B cell interaction.
系统性红斑狼疮(SLE)是一种会自发产生的典型自身免疫性疾病,在理解其基本发病机制方面向前迈出的重要一步是,确认核小体是该疾病中的主要免疫原。SLE中致病性自身抗体的产生源于特定群体的辅助性T细胞与对核小体成分具有特异性的B细胞之间受MHC-II类分子限制的同源相互作用。这些发现为阻断这种致病性T细胞与B细胞相互作用的特异性免疫疗法铺平了道路。