Literature DB >> 23318699

Treatment options for C3 glomerulopathy.

Carla M Nester1, Richard J Smith.   

Abstract

PURPOSE OF REVIEW: The purpose of this review is to discuss emerging nomenclature, review the salient clinicopathological features and describe the therapeutic options available for the treatment of C3 glomerulopathy (C3G). RECENT
FINDINGS: C3G is minimally responsive to traditional immune suppression and randomized controlled trials to support therapy are absent. The burgeoning understanding of the role of the alternative complement pathway in C3G combined with animal data supporting the use of terminal complement blockade and a few reports suggesting that the anticomplement drug eculizumab may offer a therapeutic advantage have triggered great interest in the field of complement-mediated renal disease.
SUMMARY: Anticellular immune suppression and plasma therapy have limited efficacy in C3G. Data suggest that eculizumab may ameliorate disease in some C3G patients. The limited, recently published cohort data highlight crucial aspects of this group of diseases and support the need for extensive genetic and biomarker research to validate the pathologic mechanisms, delineate the spectrum of disease and guide the design of the rigorous trials to identify effective therapies for the treatment of C3G.

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Year:  2013        PMID: 23318699      PMCID: PMC4437761          DOI: 10.1097/MNH.0b013e32835da24c

Source DB:  PubMed          Journal:  Curr Opin Nephrol Hypertens        ISSN: 1062-4821            Impact factor:   2.894


  39 in total

1.  Dense deposit disease is not a membranoproliferative glomerulonephritis.

Authors:  Patrick D Walker; Franco Ferrario; Kensuke Joh; Stephen M Bonsib
Journal:  Mod Pathol       Date:  2007-03-30       Impact factor: 7.842

2.  Variations in the complement regulatory genes factor H (CFH) and factor H related 5 (CFHR5) are associated with membranoproliferative glomerulonephritis type II (dense deposit disease).

Authors:  M A Abrera-Abeleda; C Nishimura; J L H Smith; S Sethi; J L McRae; B F Murphy; G Silvestri; C Skerka; M Józsi; P F Zipfel; G S Hageman; R J H Smith
Journal:  J Med Genet       Date:  2005-11-18       Impact factor: 6.318

3.  Allelic variants of complement genes associated with dense deposit disease.

Authors:  Maria Asuncion Abrera-Abeleda; Carla Nishimura; Kathy Frees; Michael Jones; Tara Maga; Louis M Katz; Yuzhou Zhang; Richard J H Smith
Journal:  J Am Soc Nephrol       Date:  2011-07-22       Impact factor: 10.121

4.  Primary glomerulonephritis with isolated C3 deposits: a new entity which shares common genetic risk factors with haemolytic uraemic syndrome.

Authors:  Aude Servais; Véronique Frémeaux-Bacchi; Moglie Lequintrec; Rémi Salomon; Jacques Blouin; Bertrand Knebelmann; Jean-Pierre Grünfeld; Philippe Lesavre; Laure-Hélène Noël; Fadi Fakhouri
Journal:  J Med Genet       Date:  2006-10-03       Impact factor: 6.318

5.  Acute renal failure in dense deposit disease: complete recovery after combination therapy with immunosuppressant and plasma exchange.

Authors:  R T Krmar; U Holtbäck; T Linné; U B Berg; G Celsi; M P Söderberg; A Wernerson; A Szakos; S Larsson; L Skattum; P Bárány
Journal:  Clin Nephrol       Date:  2011-02       Impact factor: 0.975

6.  Prevention of C5 activation ameliorates spontaneous and experimental glomerulonephritis in factor H-deficient mice.

Authors:  M C Pickering; J Warren; K L Rose; F Carlucci; Y Wang; M J Walport; H T Cook; M Botto
Journal:  Proc Natl Acad Sci U S A       Date:  2006-06-12       Impact factor: 11.205

7.  Human C3 mutation reveals a mechanism of dense deposit disease pathogenesis and provides insights into complement activation and regulation.

Authors:  Rubén Martínez-Barricarte; Meike Heurich; Francisco Valdes-Cañedo; Eduardo Vazquez-Martul; Eva Torreira; Tamara Montes; Agustín Tortajada; Sheila Pinto; Margarita Lopez-Trascasa; B Paul Morgan; Oscar Llorca; Claire L Harris; Santiago Rodríguez de Córdoba
Journal:  J Clin Invest       Date:  2010-09-13       Impact factor: 14.808

8.  Y402H polymorphism of complement factor H affects binding affinity to C-reactive protein.

Authors:  Matti Laine; Hanna Jarva; Sanna Seitsonen; Karita Haapasalo; Markus J Lehtinen; Nina Lindeman; Don H Anderson; Patrick T Johnson; Irma Järvelä; T Sakari Jokiranta; Gregory S Hageman; Ilkka Immonen; Seppo Meri
Journal:  J Immunol       Date:  2007-03-15       Impact factor: 5.422

9.  Defective complement control of factor H (Y402H) and FHL-1 in age-related macular degeneration.

Authors:  Christine Skerka; Nadine Lauer; Andreas A W A Weinberger; Claudia N Keilhauer; Jürgen Sühnel; Richard Smith; Ursula Schlötzer-Schrehardt; Lars Fritsche; Stefan Heinen; Andrea Hartmann; Bernhard H F Weber; Peter F Zipfel
Journal:  Mol Immunol       Date:  2007-03-30       Impact factor: 4.407

10.  Recurrence of complement factor H-related protein 5 nephropathy in a renal transplant.

Authors:  K A Vernon; D P Gale; E Goicoechea de Jorge; A G McLean; J Galliford; A Pierides; P H Maxwell; D Taube; M C Pickering; H T Cook
Journal:  Am J Transplant       Date:  2010-11-29       Impact factor: 8.086

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  30 in total

1.  Eculizumab in Pediatric Dense Deposit Disease.

Authors:  Michiel J S Oosterveld; Mark R Garrelfs; Bernd Hoppe; Sandrine Florquin; Joris J T H Roelofs; L P van den Heuvel; Kerstin Amann; Jean-Claude Davin; Antonia H M Bouts; Pietrik J Schriemer; Jaap W Groothoff
Journal:  Clin J Am Soc Nephrol       Date:  2015-08-27       Impact factor: 8.237

2.  American Society of Nephrology clinical pathological conference.

Authors:  Kevin E Meyers; Helen Liapis; Mohamed G Atta
Journal:  Clin J Am Soc Nephrol       Date:  2014-03-20       Impact factor: 8.237

3.  Insights into the Effects of Complement Factor H on the Assembly and Decay of the Alternative Pathway C3 Proconvertase and C3 Convertase.

Authors:  Serena Bettoni; Elena Bresin; Giuseppe Remuzzi; Marina Noris; Roberta Donadelli
Journal:  J Biol Chem       Date:  2016-02-22       Impact factor: 5.157

4.  Rituximab fails where eculizumab restores renal function in C3nef-related DDD.

Authors:  Caroline Rousset-Rouvière; Mathilde Cailliez; Florentine Garaix; Daniele Bruno; Daniel Laurent; Michel Tsimaratos
Journal:  Pediatr Nephrol       Date:  2014-01-10       Impact factor: 3.714

5.  Outcome of membranoproliferative glomerulonephritis and C3-glomerulopathy in children and adolescents.

Authors:  Johannes Holle; Lena Berenberg-Goßler; Kaiyin Wu; Ortraud Beringer; Florian Kropp; Dominik Müller; Julia Thumfart
Journal:  Pediatr Nephrol       Date:  2018-09-20       Impact factor: 3.714

Review 6.  Reclassification of membranoproliferative glomerulonephritis: Identification of a new GN: C3GN.

Authors:  Maurizio Salvadori; Giuseppina Rosso
Journal:  World J Nephrol       Date:  2016-07-06

Review 7.  Kidney Diseases Associated With Alternative Complement Pathway Dysregulation and Potential Treatment Options.

Authors:  Prateek Sanghera; Mythili Ghanta; Fatih Ozay; Venkatesh K Ariyamuthu; Bekir Tanriover
Journal:  Am J Med Sci       Date:  2017-03-16       Impact factor: 2.378

Review 8.  Complement cascade and kidney transplantation: The rediscovery of an ancient enemy.

Authors:  Alberto Mella; Maria Messina; Antonio Lavacca; Luigi Biancone
Journal:  World J Transplant       Date:  2014-09-24

9.  Eculizumab therapy in a patient with dense-deposit disease associated with partial lipodystropy.

Authors:  Ozan Ozkaya; Hulya Nalcacioglu; Demet Tekcan; Gurkan Genc; Bilge Can Meydan; B Handan Ozdemir; M Kemal Baysal; Hasan Tahsin Keceligil
Journal:  Pediatr Nephrol       Date:  2014-01-26       Impact factor: 3.714

10.  Generation of multiple fluid-phase C3b:plasma protein complexes during complement activation: possible implications in C3 glomerulopathies.

Authors:  Mahalakshmi Ramadass; Berhane Ghebrehiwet; Richard J Smith; Richard R Kew
Journal:  J Immunol       Date:  2013-12-23       Impact factor: 5.422

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