C3 glomerulopathy: consensus report
Tóm tắt
Từ khóa
Tài liệu tham khảo
Fakhouri, 2010, C3 glomerulopathy: a new classification, Nat Rev Nephrol, 6, 494, 10.1038/nrneph.2010.85
Martinez-Barricarte, 2010, Human C3 mutation reveals a mechanism of dense deposit disease pathogenesis and provides insights into complement activation and regulation, J Clin Invest, 120, 3702, 10.1172/JCI43343
Gale, 2010, Identification of a mutation in complement factor H-related protein 5 in patients of Cypriot origin with glomerulonephritis, Lancet, 376, 794, 10.1016/S0140-6736(10)60670-8
Malik, 2012, A hybrid CFHR3-1 gene causes familial C3 glomerulopathy, J Am Soc Nephrol, 23, 1155, 10.1681/ASN.2012020166
Walker, 2007, Dense deposit disease is not a membranoproliferative glomerulonephritis, Mod Pathol, 20, 605, 10.1038/modpathol.3800773
Servais, 2012, Acquired and genetic complement abnormalities play a critical role in dense deposit disease and other C3 glomerulopathies, Kidney Int, 82, 454, 10.1038/ki.2012.63
Herlitz, 2012, Pathology after eculizumab in dense deposit disease and C3 GN, J Am Soc Nephrol, 23, 1229, 10.1681/ASN.2011121186
Hou, 2013, Toward a working definition of C3 Glomerulopathy by immunofluorescence
Sethi, 2012, Atypical postinfectious glomerulonephritis is associated with abnormalities in the alternative pathway of complement, Kidney Int, 83, 293, 10.1038/ki.2012.384
Strobel, 2010, Anti-factor B autoantibody in dense deposit disease, Mol Immunol, 47, 1476, 10.1016/j.molimm.2010.02.002
Chen, 2012, A novel hybrid CFHR2/CFHR5 gene develops MPGN II and provides insights into disease mechanism and therapeutic implications, Immunobiology, 217, 1131, 10.1016/j.imbio.2012.08.009
Tortajada, 2013, C3 glomerulopathy-associated CFHR1 mutation alters FHR oligomerization and complement regulation, J Clin Invest, 123, 2434, 10.1172/JCI68280
Medjeral-Thomas, 2013, A novel CFHR5 fusion protein causes C3 glomerulopathy in a family without Cypriot ancestry
Abrera-Abeleda, 2011, Allelic variants of complement genes associated with dense deposit disease, J Am Soc Nephrol, 22, 1551, 10.1681/ASN.2010080795
Paixao-Cavalcante, 2012, Sensitive and specific assays for C3 nephritic factors clarify mechanisms underlying complement dysregulation, Kidney Int, 82, 1084, 10.1038/ki.2012.250
Zhang, 2012, Causes of alternative pathway dysregulation in dense deposit disease, Clin J Am Soc Nephrol, 7, 265, 10.2215/CJN.07900811
Jokiranta, 1999, Nephritogenic lambda light chain dimer: a unique human miniautoantibody against complement factor H, J Immunol, 163, 4590, 10.4049/jimmunol.163.8.4590
Nozal, 2012, Anti-factor H antibody affecting factor H cofactor activity in a patient with dense deposit disease, Clin Kidney J, 5, 133, 10.1093/ckj/sfs002
Sethi, 2010, Dense deposit disease associated with monoclonal gammopathy of undetermined significance, Am J Kidney Dis, 56, 977, 10.1053/j.ajkd.2010.06.021
Sethi, 2010, Membranoproliferative glomerulonephritis secondary to monoclonal gammopathy, Clin J Am Soc Nephrol, 5, 770, 10.2215/CJN.06760909
Athanasiou, 2011, Familial C3 glomerulopathy associated with CFHR5 mutations: clinical characteristics of 91 patients in 16 pedigrees, Clin J Am Soc Nephrol, 6, 1436, 10.2215/CJN.09541010
Nester, 2013, Treatment options for C3 glomerulopathy, Curr Opin Nephrol Hypertens, 22, 231, 10.1097/MNH.0b013e32835da24c
Appel, 2005, Membranoproliferative glomerulonephritis type II (dense deposit disease): an update, J Am Soc Nephrol, 16, 1392, 10.1681/ASN.2005010078
Group KDIGOKGW, 2012, KDIGO Clinical Practice Guideline for Glomerulonphritis, Kidney Int (Suppl), 2, 198
Daina, 2012, Eculizumab in a patient with dense-deposit disease, N Engl J Med, 366, 1161, 10.1056/NEJMc1112273
McCaughan, 2012, Recurrent dense deposit disease after renal transplantation: an emerging role for complementary therapies, Am J Transplant, 12, 1046, 10.1111/j.1600-6143.2011.03923.x
Bomback, 2012, Eculizumab for dense deposit disease and C3 glomerulonephritis, Clin J Am Soc Nephrol, 7, 748, 10.2215/CJN.12901211
Licht, 2005, Successful plasma therapy for atypical hemolytic uremic syndrome caused by factor H deficiency owing to a novel mutation in the complement cofactor protein domain 15, Am J Kidney Dis, 45, 415, 10.1053/j.ajkd.2004.10.018
Banks, 1982, Acute renal failure in dense deposit disease: recovery after plasmapheresis, Br Med J (Clin Res Ed), 284, 1874, 10.1136/bmj.284.6332.1874-b
Krmar, 2011, Acute renal failure in dense deposit disease: complete recovery after combination therapy with immunosuppressant and plasma exchange, Clin Nephrol, 75, 4
Pickering, 2006, Prevention of C5 activation ameliorates spontaneous and experimental glomerulonephritis in factor H-deficient mice, Proc Natl Acad Sci USA, 103, 9649, 10.1073/pnas.0601094103
Vivarelli, 2012, Eculizumab for the treatment of dense-deposit disease, N Engl J Med, 366, 1163, 10.1056/NEJMc1111953
Little, 2006, Severity of primary MPGN, rather than MPGN type, determines renal survival and post-transplantation recurrence risk, Kidney Int, 69, 504, 10.1038/sj.ki.5000084