Genetic dissection of systemic lupus erythematosus pathogenesis

Evidence for functional expression of Sle3/5 by non-T cells

Eric S. Sobel, Laurence Morel, Raquel Baert, Chandra Mohan, Joel Schiffenbauer, Edward K. Wakeland

Research output: Contribution to journalArticle

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Abstract

On the non-autoimmune C57BL/6 (B6) background, the chromosome 7-derived lupus susceptibility loci Sle3 and Sle5 have been shown to mediate an elevated CD4:CD8 ratio with an increase in activated CD4+ T cells, decreased susceptibility to apoptosis, and a break in humoral tolerance. Development of subcongenic strains has subsequently shown that the elevated CD4:CD8 ratio is due to Sle3 but that both loci contribute to the development of autoantibodies. To elucidate the functional expression patterns of these loci, adoptive transfer experiments were conducted. All possible combinations of bone marrow reconstitution, including syngenic, were conducted between the congenic B6 and B6.Sle3/5 strains. It was found that the Sle3/5 locus was functionally expressed by bone marrow-derived cells, but not by host cells, and that the elevated CD4:CD8 phenotype could be reconstituted in radiation chimeras. Using Ly5-marked congenic strains and B6 host mice, additional experiments surprisingly demonstrated that the elevated CD4:CD8 ratio was neither an intrinsic property of the T cells nor of single positive thymocytes. Allotype-marked chimeras indicated that autoantibody production by B cells was also an extrinsic property, as shown by the fact that B cells without the Sle3/5 interval contributed to autoantibody production. These experiments strongly suggest that a gene within the B6.Sle3/5 interval was expressed by a bone marrow-derived, nonlymphocyte population in the thymus and periphery and was affecting T cell selection and/or survival.

Original languageEnglish (US)
Pages (from-to)4025-4032
Number of pages8
JournalJournal of Immunology
Volume169
Issue number7
StatePublished - Oct 1 2002

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CD4-CD8 Ratio
Systemic Lupus Erythematosus
Autoantibodies
Dissection
T-Lymphocytes
B-Lymphocytes
Radiation Chimera
Bone Marrow
Chromosomes, Human, Pair 7
Adoptive Transfer
Thymocytes
Bone Marrow Cells
Thymus Gland
Apoptosis
Phenotype
Population
Genes

ASJC Scopus subject areas

  • Immunology

Cite this

Genetic dissection of systemic lupus erythematosus pathogenesis : Evidence for functional expression of Sle3/5 by non-T cells. / Sobel, Eric S.; Morel, Laurence; Baert, Raquel; Mohan, Chandra; Schiffenbauer, Joel; Wakeland, Edward K.

In: Journal of Immunology, Vol. 169, No. 7, 01.10.2002, p. 4025-4032.

Research output: Contribution to journalArticle

Sobel, Eric S. ; Morel, Laurence ; Baert, Raquel ; Mohan, Chandra ; Schiffenbauer, Joel ; Wakeland, Edward K. / Genetic dissection of systemic lupus erythematosus pathogenesis : Evidence for functional expression of Sle3/5 by non-T cells. In: Journal of Immunology. 2002 ; Vol. 169, No. 7. pp. 4025-4032.
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