| First Author | Wang X | Year | 2018 |
| Journal | J Am Soc Nephrol | Volume | 29 |
| Issue | 8 | Pages | 2053-2059 |
| PubMed ID | 29895552 | Mgi Jnum | J:291005 |
| Mgi Id | MGI:6435980 | Doi | 10.1681/ASN.2018030270 |
| Citation | Wang X, et al. (2018) Prevention of Fatal C3 Glomerulopathy by Recombinant Complement Receptor of the Ig Superfamily. J Am Soc Nephrol 29(8):2053-2059 |
| abstractText | Background C3 glomerulopathy (C3G) is a life-threatening kidney disease caused by dysregulation of the alternative pathway of complement (AP) activation. No approved specific therapy is available for C3G, although an anti-C5 mAb has been used off-label in some patients with C3G, with mixed results. Thus, there is an unmet medical need to develop other inhibitors of complement for C3G.Methods We used a murine model of lethal C3G to test the potential efficacy of an Fc fusion protein of complement receptor of the Ig superfamily (CRIg-Fc) in the treatment of C3G. CRIg-Fc binds C3b and inhibits C3 and C5 convertases of the AP. Mice with mutations in the factor H and properdin genes (FH(m/m)P(-/-)) develop early-onset C3G, with AP consumption, high proteinuria, and lethal crescentic GN.Results Treatment of FH(m/m)P(-/-) mice with CRIg-Fc, but not a control IgG, inhibited AP activation and diminished the consumption of plasma C3, factor B, and C5. CRIg-Fc-treated FH(m/m)P(-/-) mice also had significantly improved survival and reduced proteinuria, hematuria, BUN, glomerular C3 fragment, C9 and fibrin deposition, and GN pathology scores.Conclusions Therapeutics developed on the basis of the mechanism of action of soluble CRIg may be effective for the treatment of C3G and should be explored clinically. |
