One approach to defining the pathogenic mechanisms that cause systemic lupus erythematosus (SLE) is to determine the nature of the genetic contributions predisposing to disease. We have identified in (NZBxNZW)F2 crosses, eight loci designated Slebw-1 to -8, on chromosomes 17, 4, 5, 6, 7, 18, 1, and 11 respectively, that are linked to SLE disease susceptibility and two loci (Splbw-1 and -2) on chromosomes 1 and 4, that predispose to splenomegaly. Five of the disease susceptibility loci (Slebw-1, -2, -5, -7 and -8) were dominantly inherited and thus play a role in (NZBxNZW)F1 hybrid mice, the murine model of SLE that most closely resembles human disease.
The aims of this proposal are to define the extent of each of these loci's contribution to autoimmunity and to identify the genes involved. To accomplish this, congenic lines of NZB or NZW mice that have one of the dominantly inherited susceptibility loci replaced by the counterpart non-auto immune locus will be generated and F1 hybrids derived from these congenic lines and/or their derivatives will be examined. To identify susceptibility genes, we will screen all genes in the regions of mapped loci that appear likely candidates. If susceptibility genes are not identified by this approach, we will positionally clone Slebw-2/Splbw-2, on chromosome 4, a gene that appears to be required for early mortality, and that is also linked to glomerulonephritis and splenomegaly. The role of this gene or others identified by the candidate approach will be further substantiated in transgenic mice. Identification and characterization of the nature of autoimmune-susceptibility genes will be of profound importance in our efforts to comprehend and resolve the etiopathogenesis of the genetically-imposed autoimmmune diseases.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Research Project (R01)
Project #
1R01AR042242-01A2
Application #
2081417
Study Section
Immunological Sciences Study Section (IMS)
Project Start
1995-09-30
Project End
1999-08-31
Budget Start
1995-09-30
Budget End
1996-08-31
Support Year
1
Fiscal Year
1995
Total Cost
Indirect Cost
Name
Scripps Research Institute
Department
Type
DUNS #
City
La Jolla
State
CA
Country
United States
Zip Code
92037
Scatizzi, John C; Haraldsson, Maria K; Pollard, K Michael et al. (2012) The Lbw2 locus promotes autoimmune hemolytic anemia. J Immunol 188:3307-14
Pollard, Kenneth M; Hultman, Per; Toomey, Christopher B et al. (2011) ?2-microglobulin is required for the full expression of xenobiotic-induced systemic autoimmunity. J Immunotoxicol 8:228-37
Zuo, Li; Fulkerson, Patricia C; Finkelman, Fred D et al. (2010) IL-13 induces esophageal remodeling and gene expression by an eosinophil-independent, IL-13R alpha 2-inhibited pathway. J Immunol 185:660-9
Arandjelovic, Sanja; Wickramarachchi, Dilki; Hemmers, Saskia et al. (2010) Mast cell function is not altered by Coronin-1A deficiency. J Leukoc Biol 88:737-45
Pollard, K Michael; Hultman, Per; Kono, Dwight H (2010) Toxicology of autoimmune diseases. Chem Res Toxicol 23:455-66
Aït-Azzouzene, Djemel; Kono, Dwight H; Gonzalez-Quintial, Rosana et al. (2010) Deletion of IgG-switched autoreactive B cells and defects in Fas(lpr) lupus mice. J Immunol 185:1015-27
Kono, Dwight H; Haraldsson, M Katarina; Lawson, Brian R et al. (2009) Endosomal TLR signaling is required for anti-nucleic acid and rheumatoid factor autoantibodies in lupus. Proc Natl Acad Sci U S A 106:12061-6
Haraldsson, M Katarina; Louis-Dit-Sully, Christine A; Lawson, Brian R et al. (2008) The lupus-related Lmb3 locus contains a disease-suppressing Coronin-1A gene mutation. Immunity 28:40-51
Santiago-Raber, Marie-Laure; Haraldsson, M Katarina; Theofilopoulos, Argyrios N et al. (2007) Characterization of reciprocal Lmb1-4 interval MRL-Faslpr and C57BL/6-Faslpr congenic mice reveals significant effects from Lmb3. J Immunol 178:8195-202
Kono, Dwight H; Theofilopoulos, Argyrios N (2006) Genetics of SLE in mice. Springer Semin Immunopathol 28:83-96

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