The present review focuses on pathogenic molecular and transcriptional events in patients with lupus nephritis. These factors are renal DNaseI, exposed chromatin fragments and the corresponding chromatin-reactive autoantibodies. Lupus nephritis is the most serious complication in human systemic lupus erythematosus, and is characterised by deposition of chromatin fragment-IgG complexes in the mesangial matrix and glomerular basement membranes. The latter deposition defines end-stage disease. This event is stringently linked to a renal-restricted shutdown of expression of the DNaseI gene, as determined by loss of DNaseI mRNA level and DNaseI enzyme activity. The major aim of the present review is to generate new therapeutic strategies based on new insight into the disease pathogenesis.
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Univ Tromso, Mol Pathol Res Grp, Inst Med Biol, Fac Hlth Sci, N-9037 Tromso, NorwayUniv Tromso, Mol Pathol Res Grp, Inst Med Biol, Fac Hlth Sci, N-9037 Tromso, Norway
Hedberg, Annica
Mortensen, Elin Synnove
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Univ Tromso, Mol Pathol Res Grp, Inst Med Biol, Fac Hlth Sci, N-9037 Tromso, NorwayUniv Tromso, Mol Pathol Res Grp, Inst Med Biol, Fac Hlth Sci, N-9037 Tromso, Norway
Mortensen, Elin Synnove
Rekvig, Ole Petter
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Univ Tromso, Mol Pathol Res Grp, Inst Med Biol, Fac Hlth Sci, N-9037 Tromso, NorwayUniv Tromso, Mol Pathol Res Grp, Inst Med Biol, Fac Hlth Sci, N-9037 Tromso, Norway