| First Author | Marshak-Rothstein A | Year | 2004 |
| Journal | J Endotoxin Res | Volume | 10 |
| Issue | 4 | Pages | 247-51 |
| PubMed ID | 15373969 | Mgi Jnum | J:121909 |
| Mgi Id | MGI:3712619 | Doi | 10.1179/096805104225005850 |
| Citation | Marshak-Rothstein A, et al. (2004) Comparison of CpG s-ODNs, chromatin immune complexes, and dsDNA fragment immune complexes in the TLR9-dependent activation of rheumatoid factor B cells. J Endotoxin Res 10(4):247-51 |
| abstractText | Synthetic single-stranded oligodeoxynucleotides (15-30 bp) containing CpG motifs and phosphorothioate backbones (CpG s-ODN), immune complexes consisting of anti-nucleosome mAbs and mammalian chromatin (chromatin IC), and immune complexes consisting of anti-hapten mAbs and haptenated-double stranded DNA fragments ( approximately 600 bp) can all effectively stimulate transgenic B cells expressing a rheumatoid factor receptor by a TLR9-dependent process. However, differential sensitivity to both s-ODN and small molecule inhibitors suggests that stimulatory CpG sODN and chromatin IC may either access TLR9 via different routes or depend on discrete activation parameters. These data have important implications regarding the therapeutic application of TLR9 inhibitors to the treatment of systemic autoimmune diseases. |
