Abrogation of lupus nephritis in activation-induced deaminase-deficient MRL/lpr mice

C Jiang, J Foley, N Clayton, G Kissling… - The Journal of …, 2007 - journals.aai.org
C Jiang, J Foley, N Clayton, G Kissling, M Jokinen, R Herbert, M Diaz
The Journal of Immunology, 2007journals.aai.org
We generated MRL/lpr mice deficient in activation-induced deaminase (AID). Because AID
is required for Ig hypermutation and class switch recombination, these mice lack
hypermutated IgG Abs. Unlike their AID wild-type littermates, AID-deficient MRL/lpr mice not
only lacked autoreactive IgG Abs but also experienced a dramatic increase in the levels of
autoreactive IgM. This phenotype in AID-deficient mice translated into a significant reduction
in glomerulonephritis, minimal mononuclear cell infiltration in the kidney, and a dramatic …
Abstract
We generated MRL/lpr mice deficient in activation-induced deaminase (AID). Because AID is required for Ig hypermutation and class switch recombination, these mice lack hypermutated IgG Abs. Unlike their AID wild-type littermates, AID-deficient MRL/lpr mice not only lacked autoreactive IgG Abs but also experienced a dramatic increase in the levels of autoreactive IgM. This phenotype in AID-deficient mice translated into a significant reduction in glomerulonephritis, minimal mononuclear cell infiltration in the kidney, and a dramatic increase in survival to levels comparable to those previously reported for MRL/lpr mice completely lacking B cells and well below those of mice lacking secreted Abs. Therefore, this study wherein littermates with either high levels of autoreactive IgM or autoreactive IgG were directly examined proves that autoreactive IgM Abs alone are not sufficient to promote kidney disease in MRL/lpr mice. In addition, the substantial decrease in mortality combined with a dramatic increase in autoreactive IgM Abs in AID-deficient MRL/lpr mice suggest that autoreactive IgM Abs might not only fail to promote nephritis but may also provide a protective role in MRL/lpr mice. This novel mouse model containing high levels of autoreactive, unmutated IgM Abs will help delineate the contribution of autoreactive IgM to autoimmunity.
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