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      Nephritic Factors: An Overview of Classification, Diagnostic Tools and Clinical Associations

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          Abstract

          Nephritic factors comprise a heterogeneous group of autoantibodies against neoepitopes generated in the C3 and C5 convertases of the complement system, causing its dysregulation. Classification of these autoantibodies can be clustered according to their stabilization of different convertases either from the classical or alternative pathway. The first nephritic factor described with the capacity to stabilize C3 convertase of the alternative pathway was C3 nephritic factor (C3NeF). Another nephritic factor has been characterized by the ability to stabilize C5 convertase of the alternative pathway (C5NeF). In addition, there are autoantibodies against assembled C3/C5 convertase of the classical and lectin pathways (C4NeF). These autoantibodies have been mainly associated with kidney diseases, like C3 glomerulopathy and immune complex-associated-membranoproliferative glomerulonephritis. Other clinical situations where these autoantibodies have been observed include infections and autoimmune disorders such as systemic lupus erythematosus and acquired partial lipodystrophy. C3 hypocomplementemia is a common finding in all patients with nephritic factors. The methods to measure nephritic factors are not standardized, technically complex, and lack of an appropriate quality control. This review will be focused in the description of the mechanism of action of the three known nephritic factors (C3NeF, C4NeF, and C5NeF), and their association with human diseases. Moreover, we present an overview regarding the diagnostic tools for its detection, and the main therapeutic approach for the patients with nephritic factors.

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          Overview of Complement Activation and Regulation

          Summary Complement is an important component of the innate immune system that is crucial for defense from microbial infections and for clearance of immune complexes and injured cells. In normal conditions complement is tightly controlled by a number of fluid-phase and cell surface proteins to avoid injury to autologous tissues. When complement is hyperactivated, as occurs in autoimmune diseases or in subjects with dysfunctional regulatory proteins, it drives a severe inflammatory response in numerous organs. The kidney appears to be particularly vulnerable to complement-mediated inflammatory injury. Injury may derive from deposition of circulating active complement fragments in glomeruli, but complement locally produced and activated in the kidney also may have a role. Many kidney disorders have been linked to abnormal complement activation, including immune-complex–mediated glomerulonephritis and rare genetic kidney diseases, but also tubulointerstitial injury associated with progressive proteinuric diseases or ischemia-reperfusion.
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            C3 glomerulopathy: consensus report

            C3 glomerulopathy is a recently introduced pathological entity whose original definition was glomerular pathology characterized by C3 accumulation with absent or scanty immunoglobulin deposition. In August 2012, an invited group of experts (comprising the authors of this document) in renal pathology, nephrology, complement biology, and complement therapeutics met to discuss C3 glomerulopathy in the first C3 Glomerulopathy Meeting. The objectives were to reach a consensus on: the definition of C3 glomerulopathy, appropriate complement investigations that should be performed in these patients, and how complement therapeutics should be explored in the condition. This meeting report represents the current consensus view of the group.
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              Novel mechanisms and functions of complement

              Progress in the beginning of the 21 st century transformed our perception of complement from a blood-based antimicrobial system to a global regulator of immunity and tissue homeostasis. More recent years have witnessed remarkable advances regarding structure-function insights, mechanisms and locations of complement activation, thereby adding new layers of complexity in the biology of complement. This complexity is readily reflected by the multifaceted and contextual involvement of complement-driven networks in a wide range of inflammatory and neurodegenerative disorders and cancer. This Review provides an updated view of new and previously unanticipated functions of complement and how these impact immunity and disease pathogenesis.
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                Author and article information

                Contributors
                Journal
                Front Immunol
                Front Immunol
                Front. Immunol.
                Frontiers in Immunology
                Frontiers Media S.A.
                1664-3224
                24 April 2019
                2019
                : 10
                : 886
                Affiliations
                [1] 1Complement Research Group, Hospital La Paz Institute for Health Research (IdiPAZ), La Paz University Hospital , Madrid, Spain
                [2] 2Center for Biomedical Network Research on Rare Diseases (CIBERER U754) , Madrid, Spain
                [3] 3Department of Medical Biotechnology, Intercollegiate Faculty of Biotechnology, University of Gdansk and Medical University of Gdansk , Gdansk, Poland
                [4] 4Immunology Unit, La Paz University Hospital , Madrid, Spain
                [5] 5Pediatric Nephrology Unit, La Paz University Hospital , Madrid, Spain
                [6] 6Departamento de Medicina, Universidad Autónoma de Madrid , Madrid, Spain
                Author notes

                Edited by: Marie-Agnes Dragon-Durey, Université Paris Descartes, France

                Reviewed by: Sophie Chauvet, INSERM U1138 Centre de Recherche des Cordeliers, France; Betty P. Tsao, Medical University of South Carolina, United States

                *Correspondence: Margarita López-Trascasa margarita.lopez@ 123456uam.es

                This article was submitted to Autoimmune and Autoinflammatory Disorders, a section of the journal Frontiers in Immunology

                Article
                10.3389/fimmu.2019.00886
                6491685
                31068950
                c35c4b26-55b1-4cbd-8591-c51208f85ece
                Copyright © 2019 Corvillo, Okrój, Nozal, Melgosa, Sánchez-Corral and López-Trascasa.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 30 November 2018
                : 05 April 2019
                Page count
                Figures: 3, Tables: 1, Equations: 0, References: 155, Pages: 14, Words: 11582
                Funding
                Funded by: Ministerio de Economía, Industria y Competitividad, Gobierno de España 10.13039/501100010198
                Award ID: PI15/00255
                Award ID: PI16-00723
                Categories
                Immunology
                Review

                Immunology
                complement system,nephritic factor,c3 glomerulopathy,lipodystrophy,eculizumab
                Immunology
                complement system, nephritic factor, c3 glomerulopathy, lipodystrophy, eculizumab

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