| Literature DB >> 1832281 |
M Goldman1, P Druet, E Gleichmann.
Abstract
Systemic autoimmune diseases can be induced experimentally in rodents by graft-versus-host or host-versus-graft reactions and by chemicals such as HgCl2, gold salts and D-penicillamine. These models share several features, such as productions of anti-nuclear antibodies, immune glomerulonephritis, MHC class II hyperexpression on B cells, hyper-IgE, increased IL-4 activity and impairment of IL-2 production. This profile of cytokines suggests a central role for TH2-type cells in their pathogenesis. Here, Michel Goldman and colleagues review the data supporting this hypothesis and discuss the possible molecular bases for T-cell activation in chemically-induced systemic autoimmunity.Entities:
Mesh:
Year: 1991 PMID: 1832281 DOI: 10.1016/0167-5699(91)90034-Q
Source DB: PubMed Journal: Immunol Today ISSN: 0167-5699