TY - JOUR
T1 - Toll-like receptor 9-independent aggravation of glomerulonephritis in a novel model of SLE
AU - Yu, Philipp
AU - Wellmann, Ute
AU - Kunder, Sandra
AU - Quintanilla-Martinez, Leticia
AU - Jennen, Luise
AU - Dear, Neil
AU - Amann, Kerstin
AU - Bauer, Stefan
AU - Winkler, Thomas H.
AU - Wagner, Hermann
N1 - Funding Information:
We thank H. Drexler and E. Samson, J. Müller and C. Kloss for excellent technical assistance and A. Marshak-Rothstein and G. Häcker for critical reading of the manuscript. This work was supported by the NGFN2 grant (01GR0430). U.W., K.A. and T.H.W. are supported by the Deutsche Forschungsgemeinschaft through SFB 423, DFG SPP 1110 (S.B.) and SFB456 (H.W. and S.B.). We thank Ingenium Pharmaceuticals AG, Martinsried for providing us with Ali5 mice.
PY - 2006/8
Y1 - 2006/8
N2 - The generation of anti-DNA auto-antibodies is characteristic for the human autoimmune condition systemic lupus erythematosus (SLE) and its animal models. However, the contribution of the toll-like receptor (TLR) system of innate immunity receptors and, in particular, TLR9 to this B cell-mediated autoimmune process remains controversial. Here we report that in a novel murine model of SLE, based on hyper-reactive B cell activation mediated by mutant phospholipase Cg2, the genetic deficiency of TLR9 does not protect from spontaneous anti-DNA auto-antibody formation and glomerulonephritis. On the contrary, disease induction is aggravated and additional nucleolar antibody specificity develops in autoimmune TLR9-deficient mice. In vitro studies demonstrate that, in autoimmune-prone mice, dual signaling via the B cell receptor and non-CpG DNA results in synergistic B cell activation in a TLR9-independent manner. These results suggest that engagement of a TLR9-independent DNA activation pathway may promote autoimmunity, while TLR9 signaling can ameliorate SLE-like immune pathology in vivo.
AB - The generation of anti-DNA auto-antibodies is characteristic for the human autoimmune condition systemic lupus erythematosus (SLE) and its animal models. However, the contribution of the toll-like receptor (TLR) system of innate immunity receptors and, in particular, TLR9 to this B cell-mediated autoimmune process remains controversial. Here we report that in a novel murine model of SLE, based on hyper-reactive B cell activation mediated by mutant phospholipase Cg2, the genetic deficiency of TLR9 does not protect from spontaneous anti-DNA auto-antibody formation and glomerulonephritis. On the contrary, disease induction is aggravated and additional nucleolar antibody specificity develops in autoimmune TLR9-deficient mice. In vitro studies demonstrate that, in autoimmune-prone mice, dual signaling via the B cell receptor and non-CpG DNA results in synergistic B cell activation in a TLR9-independent manner. These results suggest that engagement of a TLR9-independent DNA activation pathway may promote autoimmunity, while TLR9 signaling can ameliorate SLE-like immune pathology in vivo.
KW - Autoimmunity
KW - B cells
KW - Innate immunity
KW - Systemic lupus erythematosus
UR - http://www.scopus.com/inward/record.url?scp=33748465308&partnerID=8YFLogxK
U2 - 10.1093/intimm/dxl067
DO - 10.1093/intimm/dxl067
M3 - Article
C2 - 16798839
AN - SCOPUS:33748465308
SN - 0953-8178
VL - 18
SP - 1211
EP - 1219
JO - International Immunology
JF - International Immunology
IS - 8
ER -