Abstract
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 clas-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.
Original language | English (US) |
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Pages (from-to) | 132-147 |
Number of pages | 16 |
Journal | Immunologic Research |
Volume | 14 |
Issue number | 2 |
DOIs | |
State | Published - Jun 1995 |
Keywords
- Anti-DNA autoantibodies
- Autoimmune T cell receptors
- CD40
- CD40-ligand
- Immunotherapy
- Systemic lupus erythematosus
ASJC Scopus subject areas
- Immunology