Constitutive expression of interleukin (IL)-4 in vivo causes autoimmune-type disorders in mice
| Autor: | A Schimpl, Klaus J. Erb, K Rivett, M von Brevern, B Rüger, B Ryffel |
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| Rok vydání: | 1997 |
| Předmět: |
Immunology
Mice Transgenic Major histocompatibility complex Lymphocyte Activation Article Autoimmune Diseases Mice Immune system MHC class I Superantigen medicine Immunology and Allergy Animals Interleukin 4 B cell Autoantibodies MHC class II B-Lymphocytes Superantigens biology Interleukin Articles medicine.anatomical_structure biology.protein Female Interleukin-4 |
| Zdroj: | The Journal of Experimental Medicine |
| ISSN: | 0022-1007 |
| Popis: | The transgenic (tg) expression of interleukin (IL)-4 under the control of a major histocompatibility complex (MHC) class I promoter leads to B cell hyperactivity in mice, characterized by increased B cell surface MHC class II and CD23 expression, elevated responsiveness of the B cells to polyclonal ex vivo stimulation, and increased immunoglobulin (Ig)G1 and IgE serum levels. Tg mice develop anemia, glomerulonephritis with complement and immune deposition in the glomeruli, and show increased production of autoantibodies. Treatment of IL-4 tg mice with anti-IL-4 neutralizing antibodies protected the mice from disease development, showing that IL-4 was responsible for the observed disorders. Deletion of superantigen responsive autoreactive T cells in the IL-4 tg mice was normal and treatment of mutant mice with deleting anti-CD4 antibodies failed to ablate the onset of autoimmune-like disease, suggesting that CD4+T cells were not the primary cause of the disorders. Furthermore, the deletion of B cells reacting against MHC class I molecules was also normal in the IL-4 tg mice. Therefore the most likely explanation for the increased production of autoantibodies and the autoimmunelike disorders is that IL-4 acts directly on autoreactive B cells by expanding them in a polyclonal manner. Taken together our results show that inappropriate multi-organ expression of IL-4 in vivo leads to autoimmune-type disease in mice. |
| Databáze: | OpenAIRE |
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