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Updated: May 16, 2026

The bm12 Inducible Model of Systemic Lupus Erythematosus (SLE) in C57BL/6 Mice
Published on: November 1, 2015
[Childhood-onset systemic lupus erythematosus: polygenic or monogenic disorder?]
B Bader-Meunier1, N Jeremiah, F Rieux-Laucat
1Service d'immunologie et rhumatologie pédiatrique, hôpital Necker, 149, rue de Sèvres, 75015 Paris, France. brigitte.bader-meunier@nck.aphp.fr
Abstract:
Systemic lupus erythematosus (SLE) results from the complex interaction between genetic and environmental factors. It is usually thought that SLE results from the combined effect of variants in a large number of genes, and several genome whole association studies (GWAS) have identified a great number of single-nucleotide polymorphisms (SNP) associated with SLE. However, the loci identified so far can account for only about 15% of the heritability of SLE. Recently, some Mendelian variants of lupus have been identified, especially in childhood-onset SLE. Children present with more severe illness, a lower sex-ratio female:male and a higher genetic contribution compared to adults with SLE. pSLE phenotype heterogeneity could be related to genetic heterogeneity, and pSLE in part might consist in a collection of rare, genetically distinct monogenic disorders.
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