Journal of the American Society of Nephrology
2007 JASN IMPACT FACTOR 7.111 HOME   AUTHOR INFO   EDITORIAL BOARD   SUBSCRIBE   FEEDBACK   ALERTS   HELP 
    advanced
CURRENT ISSUE ARCHIVES JASN Express ONLINE SUBMISSION


This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Bao, L.
Right arrow Articles by Quigg, R. J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Bao, L.
Right arrow Articles by Quigg, R. J.
J Am Soc Nephrol 14:670-679, 2003
© 2003 American Society of Nephrology

Administration of a Soluble Recombinant Complement C3 Inhibitor Protects Against Renal Disease in MRL/lpr Mice

Lihua Bao*, Mark Haas{dagger}, Damian M. Kraus{ddagger}, Bradley K. Hack*, Jonathan K. Rakstang{ddagger}, V. Michael Holers{ddagger} and Richard J. Quigg*

*Section of Nephrology, The University of Chicago, Chicago, Illinois; {dagger}Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland; {ddagger}Division of Rheumatology, University of Colorado Health Sciences Center, Denver, Colorado.

Correspondence to Dr. Richard J. Quigg, Section of Nephrology, The University of Chicago, 5841 S. Maryland Ave., MC5100, Chicago, IL 60637. Phone: 773-702-0757; Fax: 773-702-4816;

ABSTRACT. Complement receptor 1-related gene/protein y (Crry) in rodents is a potent membrane complement regulator that inhibits complement C3 activation by both classical and alternative pathways. To clarify the role of complement in lupus nephritis, MRL/lpr mice were given Crry as a recombinant protein (Crry-Ig) from 12 to 24 wk of age. Control groups were given saline or normal mouse IgG. Sera and urine were collected biweekly. Only 1 of 20 (5%) Crry-Ig-treated mice developed renal failure (BUN > 50 mg/dl) compared with 18 of 38 (47.4%) mice in control groups (P = 0.001). BUN levels at 24 wk were reduced from 68.8 ± 9.7 mg/dl in control groups to 38.5 ± 3.9 mg/dl in the Crry-Ig-treated group (P < 0.01). Urinary albumin excretion at 24 wk was also significantly reduced from 5.3 ± 1.4 mg/mg creatinine in the control groups to 0.5 ± 0.2 mg/mg creatinine in the Crry-Ig-treated group (P < 0.05). Of the histologic data at 24 wk, there was a significant reduction in scores for glomerulosclerosis and C3d, IgG, IgG3, and IgA staining intensity in glomeruli in complement-inhibited animals. Crry-Ig-treated animals were also protected from vasculitic lesions. Although there was no effect on relevant autoimmune manifestations such as anti-double stranded DNA titers or cryoglobulin IgG3 levels, circulating immune complex levels were markedly higher in complement-inhibited animals. Thus, inhibition of complement activation with Crry-Ig significantly reduces renal disease in MRL/lpr lupus mice. The data support the strategy of using recombinant complement C3 inhibitors to treat human lupus nephritis. E-mail: rquigg@medicine.uchicago.edu




This article has been cited by other articles:


Home page
J. Immunol.Home page
C. Atkinson, F. Qiao, H. Song, G. S. Gilkeson, and S. Tomlinson
Low-Dose Targeted Complement Inhibition Protects against Renal Disease and Other Manifestations of Autoimmune Disease in MRL/lpr Mice
J. Immunol., January 15, 2008; 180(2): 1231 - 1238.
[Abstract] [Full Text] [PDF]


Home page
J. Immunol.Home page
H. Song, F. Qiao, C. Atkinson, V. M. Holers, and S. Tomlinson
A Complement C3 Inhibitor Specifically Targeted to Sites of Complement Activation Effectively Ameliorates Collagen-Induced Arthritis in DBA/1J Mice
J. Immunol., December 1, 2007; 179(11): 7860 - 7867.
[Abstract] [Full Text] [PDF]


Home page
Nephrol Dial TransplantHome page
M. Nangaku
A Crry for polar shedding
Nephrol. Dial. Transplant., July 1, 2006; 21(7): 1773 - 1775.
[Full Text] [PDF]


Home page
FASEB J.Home page
C. A. Farrar, W. Zhou, T. Lin, and S. H. Sacks
Local extravascular pool of C3 is a determinant of postischemic acute renal failure
FASEB J, February 1, 2006; 20(2): 217 - 226.
[Abstract] [Full Text] [PDF]


Home page
J. Immunol.Home page
J. M. Thurman and V. M. Holers
The Central Role of the Alternative Complement Pathway in Human Disease
J. Immunol., February 1, 2006; 176(3): 1305 - 1310.
[Abstract] [Full Text] [PDF]


Home page
J. Immunol.Home page
J. J. Alexander, A. Jacob, L. Bao, R. L. Macdonald, and R. J. Quigg
Complement-Dependent Apoptosis and Inflammatory Gene Changes in Murine Lupus Cerebritis
J. Immunol., December 15, 2005; 175(12): 8312 - 8319.
[Abstract] [Full Text] [PDF]


Home page
J. Am. Soc. Nephrol.Home page
S. E. Wenderfer, B. Ke, T. J. Hollmann, R. A. Wetsel, H. Y. Lan, and M. C. Braun
C5a Receptor Deficiency Attenuates T Cell Function and Renal Disease in MRLlpr Mice
J. Am. Soc. Nephrol., December 1, 2005; 16(12): 3572 - 3582.
[Abstract] [Full Text] [PDF]


Home page
J. Immunol.Home page
L. Bao, I. Osawe, M. Haas, and R. J. Quigg
Signaling through Up-Regulated C3a Receptor Is Key to the Development of Experimental Lupus Nephritis
J. Immunol., August 1, 2005; 175(3): 1947 - 1955.
[Abstract] [Full Text] [PDF]


Home page
J. Am. Soc. Nephrol.Home page
P. N. Cunningham and R. J. Quigg
Contrasting Roles of Complement Activation and Its Regulation in Membranous Nephropathy
J. Am. Soc. Nephrol., May 1, 2005; 16(5): 1214 - 1222.
[Abstract] [Full Text] [PDF]


Home page
Clin. Cancer Res.Home page
H. Watanabe, A. J. Mamelak, E. Weiss, B. Wang, I. Freed, A. K. Brice, L. Wachtman, K. L. Gabrielson, N. Yokota, D. J. Hicklin, et al.
Anti-Vascular Endothelial Growth Factor Receptor-2 Antibody Accelerates Renal Disease in the NZB/W F1 Murine Systemic Lupus Erythematosus Model
Clin. Cancer Res., January 1, 2005; 11(1): 407 - 409.
[Full Text] [PDF]


Home page
J. Am. Soc. Nephrol.Home page
J. J. Alexander, M. C. Pickering, M. Haas, I. Osawe, and R. J. Quigg
Complement Factor H Limits Immune Complex Deposition and Prevents Inflammation and Scarring in Glomeruli of Mice with Chronic Serum Sickness
J. Am. Soc. Nephrol., January 1, 2005; 16(1): 52 - 57.
[Abstract] [Full Text] [PDF]


Home page
J. Immunol.Home page
R. J. Quigg
Complement and the Kidney
J. Immunol., October 1, 2003; 171(7): 3319 - 3324.
[Full Text] [PDF]


Home page
J. Am. Soc. Nephrol.Home page
L. Bao, J. Zhou, V. M. Holers, and R. J. Quigg
Excessive Matrix Accumulation in the Kidneys of MRL/lpr Lupus Mice Is Dependent on Complement Activation
J. Am. Soc. Nephrol., October 1, 2003; 14(10): 2516 - 2525.
[Abstract] [Full Text] [PDF]


Home page
J. Am. Soc. Nephrol.Home page
M. Nangaku
Complement Regulatory Proteins: Are They Important in Disease?
J. Am. Soc. Nephrol., September 1, 2003; 14(9): 2411 - 2413.
[Full Text] [PDF]


Home page
J. Am. Soc. Nephrol.Home page
W. G. Couser
Complement Inhibitors And Glomerulonephritis: Are We There Yet?
J. Am. Soc. Nephrol., March 1, 2003; 14(3): 815 - 818.
[Full Text] [PDF]




HOME CURRENT ISSUE ARCHIVES JASN Express ONLINE SUBMISSION AUTHOR INFO
EDITORIAL BOARD SUBSCRIBE FEEDBACK ALERTS HELP