Aβ t cell-dependent and -independent contributions to autoimmunity in lupus-prone mrump-lpr/lprwce
- S. Penget,
- M. Madaio,
- S. D. Hughes,
- N. Crispe,
- M. Owenï,
- A. Haydays
- Unknown
Abstract
MRL/Mp-/pr)rmice develop a spontaneous lupus syndrome, including glomerulonephritis, hypergammaglobulinemia, and lymphadenopathy, as well as the production of anti-double stranded (ds) DNA, anti-small nuclear ribonucleoprotein particles (snRNP), and rheumatoid factor (RF) antibodies. To investigate the role of lymphocyte subsets in the pathogenesis of disease, MRL/lpr mice were made deficient in aβ T cells via the backcrossing of a TCR a -/- mutation. Examined at twelve and eighteen weeks, TCR a -/- MRL/Mp-/pr/îpr mice developed reduced lymphadenopathy, hypergammaglobulinemia, autoantibodies, and glomerulonephritis in comparison to wildtype animals. Still, they still generated a partially penetrant form of lupus, characterized by minimal lymphadenopathy, elevated levels of class-switched immunoglobulins, increased incidences of antinuclear antibodies as assayed by immunofluorescence, and immune deposits in kidneys. While TCR a -/- animals developed grossly reduced levels of rheumatoid factor, they produced anti-snRNP antibodies with frequencies similar to that of controls, as well as as partial autoimmunity to dsDNA, characterized by ELIS Apositive, but Crithidia kinetoplast-negative antibodies. These findings demonstrate that murine lupus in the setting of Fas-deficiency does not absolutely require the presence of aβ T cells. They also suggest that a significant basis for MRLJIpr disease, including renal immune deposits, involves aβ T cell-independent, polyreactive B cell autoimmunity, upon which aβ T cell-dependent mechanisms aggravate specific autoimmune responses.
Publication Information
Output type
Original language
English (US)Pages from-to (Number of pages)
Pages 222aJournal (Volume, Issue Number)
Journal of Investigative Medicine (Volume 44, Issue 3)Publication milestones
- Published - 1996
Publication status
ISSN
1081-5589Publication IDs
- Scopus: 33749444151
