Complement Pathways in Membranous Nephropathy: Complex and Multifactorial

Abstract

See Clinical Research on Page 618 See Clinical Research on Page 618 Membranous nephropathy (MN) is a rare, but severe autoimmune kidney disease and a major cause of nephrotic syndrome in adults. Clinically defined by nephrotic syndrome, which is persistent in approximately two-thirds of untreated patients, it manifests histologically by subepithelial immune deposits at the glomerular basement membrane in the kidney containing IgGs. MN can be idiopathic (or primary, iMN) without any identified cause (70%–80% of cases), or secondary (sMN) to clinical disorders such as hepatitis B, systematic lupus erythematosus, cancer, or drug side effects. Etiology of iMN has remained elusive for decades, until recently when several groups discovered different podocyte antigens, such as a neutral endopeptidase in rare cases in the neonate in 2002, M-type phospholipase A2 receptor (PLA2R1) in 70% of patients with iMN in 2009, thrombospondin type-1 domain-containing 7A in 2% to 5% of patients with iMN in 2014, exostosin 1 and exostosin 2 (EXT1 and EXT2, respectively) in 30% to 40% of patients with sMN in 2019, and NELL-1 in 2% to 7% of patients with iMN in 2020.1Ahmad S.B. Appel G.B. Antigens, antibodies, and membranous nephropathy: a decade of progress.Kidney Int. 2020; 97: 29-31Abstract Full Text Full Text PDF PubMed Scopus (8) Google Scholar Since the discovery of antibodies against these antigens, much has been learned about their prognostic value, and several genome-wide association studies have discovered disease-related variants associated with a higher risk of MN; however, the pathogenicity of MN remains largely unexplored. The complement system plays an important role in a variety of autoimmune diseases, including MN. A number of proteins are involved and sequentially activated following an immune trigger, finally leading to the formation of the membrane attack complex C5b-9. Three major complement pathways have been described: classical and lectin pathways are usually activated following an immune trigger, whereas the alternative pathway is continuously activated at low level (Figure 1).2Cybuisky A.V. Rennke H.G. Feintzeig I.D. Salant D.J. Complement-induced glomerular epithelial cell injury. Role of the membrane attack complex in rat membranous nephropathy.J Clin Invest. 1986; 77: 1096-1107Crossref PubMed Google Scholar, 3Tomas N.M. Hoxha E. Reinicke A.T. et al.Autoantibodies against thrombospondin type-1 domain-containing 7A induce membranous nephropathy.J Clin Invest. 2016; 126: 2519-2532Crossref PubMed Scopus (104) Google Scholar, 4Bally S. Debiec H. Ponard D. et al.Phospholipase A2 receptor-related membranous nephropathy and mannan-binding lectin deficiency.J Am Soc Nephrol. 2016; 27: 3539-3544Crossref PubMed Scopus (43) Google Scholar, 5Luo W. Olaru F. Miner J.H. et al.Alternative pathway is essential for glomerular complement activation and proteinuria in a mouse model of membranous nephropathy.Front Immunol. 2018; 9: 1433Crossref PubMed Scopus (19) Google Scholar, 6Lateb M. Ouahmi H. Payré C. et al.Anti-PLA2R1 antibodies containing sera induce in vitro cytotoxicity mediated by complement activation.J Immunol Res. 2019; 2019: 1324804Crossref PubMed Scopus (9) Google Scholar, 7Ravindran A. Madden B. Charlesworth M.C. et al.Proteomic analysis of complement proteins in membranous nephropathy.Kidney Int Rep. 2020; 5: 618-626Abstract Full Text Full Text PDF PubMed Scopus (15) Google Scholar, 8Hayashi N. Okada K. Matsui Y. et al.Glomerular mannose-binding lectin deposition in intrinsic antigen-related membranous nephropathy.Nephrol Dial Transplant. 2018; 33: 832-840Crossref PubMed Scopus (24) Google Scholar Proteinuria in patients with MN is probably a result of podocyte injury and complement activation, notably because of the destructive action of C5b-9 at the glomerular basement membrane, as has been nicely demonstrated in Heymann nephritis, a rat model of MN.2Cybuisky A.V. Rennke H.G. Feintzeig I.D. Salant D.J. Complement-induced glomerular epithelial cell injury. Role of the membrane attack complex in rat membranous nephropathy.J Clin Invest. 1986; 77: 1096-1107Crossref PubMed Google Scholar The pathogenic nature of the antibodies in MN has recently been demonstrated by Tomas et al.,3Tomas N.M. Hoxha E. Reinicke A.T. et al.Autoantibodies against thrombospondin type-1 domain-containing 7A induce membranous nephropathy.J Clin Invest. 2016; 126: 2519-2532Crossref PubMed Scopus (104) Google Scholar who showed that injection with human anti–thrombospondin type-1 domain-containing 7A antibodies forms glomerular deposits and induces proteinuria in mice, but the complement pathways involved have not been studied. As the complement pathways in MN have remained unexplored, so has the pathogenicity of different subclasses of IgG antibodies. In most iMN cases, IgG4 is the predominant subclass, whereas IgG1 and IgG3 are present in a minority of patients. As IgG4 cannot bind C1q, a major precursor in the classical pathway, it is believed that IgG4 cannot activate the complement and therefore cannot be pathogenic. Accordingly, most patients with iMN present very weak C1q deposits. These observations suggest that the alternative and/or the lectin pathways might be involved in complement activation in iMN. Bally et al.4Bally S. Debiec H. Ponard D. et al.Phospholipase A2 receptor-related membranous nephropathy and mannan-binding lectin deficiency.J Am Soc Nephrol. 2016; 27: 3539-3544Crossref PubMed Scopus (43) Google Scholar reported that iMN can develop in patients with complete mannose-binding lectin deficiency with complement mostly activated by the alternative pathway. In line with this theory, mice without a functional alternative pathway did not exhibit glomerular deposition of C5b-9 and did not develop albuminuria, arguing that the alternative and not the classical or the lectin pathway may be crucial for the onset of proteinuria.5Luo W. Olaru F. Miner J.H. et al.Alternative pathway is essential for glomerular complement activation and proteinuria in a mouse model of membranous nephropathy.Front Immunol. 2018; 9: 1433Crossref PubMed Scopus (19) Google Scholar However, only a genetic approach was used in this study, and the planted antigen method used to induce proteinuria is more similar to sMN than to iMN. Two recent articles have tried to resolve this dilemma. The first, by Lateb et al.,6Lateb M. Ouahmi H. Payré C. et al.Anti-PLA2R1 antibodies containing sera induce in vitro cytotoxicity mediated by complement activation.J Immunol Res. 2019; 2019: 1324804Crossref PubMed Scopus (9) Google Scholar demonstrated that at least in vitro anti-PLA2R1 antibodies, but not antibodies from a healthy donor, are cytotoxic for HEK293 cells overexpressing PLA2R1 antigen in the presence of complement. In addition, the inhibition of classical and lectin pathways highly decreased, but did not completely abolish the anti-PLA2R1 antibody-mediated cytotoxicity, suggesting that the classical and lectin pathways may nevertheless be the predominant pathways in patients with iMN with anti-PLA2R1 antibodies, thus contradicting the mice study.5Luo W. Olaru F. Miner J.H. et al.Alternative pathway is essential for glomerular complement activation and proteinuria in a mouse model of membranous nephropathy.Front Immunol. 2018; 9: 1433Crossref PubMed Scopus (19) Google Scholar Sera containing only the IgG4 subclass and/or with a lower anti-PLA2R1 titer were less cytotoxic than the sera containing at least one additional IgG subclass and/or a higher anti-PLA2R1 titer, thereby indirectly confirming the hypothesis that the subclass of IgG antibodies as well as their quantity may define which complement pathway is activated and to what extent.6Lateb M. Ouahmi H. Payré C. et al.Anti-PLA2R1 antibodies containing sera induce in vitro cytotoxicity mediated by complement activation.J Immunol Res. 2019; 2019: 1324804Crossref PubMed Scopus (9) Google Scholar In iMN, multiple IgG subclasses are detected at disease onset, whereas the IgG4 subclass becomes predominant during the course of the disease, suggesting an IgG subclass switching, as already reported in other IgG4-medaited autoimmune diseases. This switch might explain the heterogeneity of complement activation profiles in patients with iMN at onset and during follow-up. The newest article, by Ravindran et al.,7Ravindran A. Madden B. Charlesworth M.C. et al.Proteomic analysis of complement proteins in membranous nephropathy.Kidney Int Rep. 2020; 5: 618-626Abstract Full Text Full Text PDF PubMed Scopus (15) Google Scholar presented in this issue, develops a novel and unique approach to study complement proteins in the biopsies of subjects with MN using mass spectrometry following laser-capture microdissection. Indeed, the number of proteins studied (complement proteins, complement-regulating proteins, and IgGs) and the quantitative data obtained are a major strength of this study, allowing for a careful dissection of complement pathways activated in situ. The groups studied include control cases (donor kidney biopsy before transplantation), patients with PLA2R1-associated iMN, and patients with EXT1/EXT2-associated sMN. As expected, PLA2R1-associated iMN presents mostly with IgG4, whereas in the secondary forms of MN, IgG1 is predominant. Despite these clear differences in IgG subclasses, the pathways activated did not seem to clearly differ between PLA2R1- and EXT1/EXT2-associated MN, suggesting that both alternative and classical pathways are activated in patients with MN (mostly detection of C3, C4, and complement-regulating proteins of the alternative pathway, whereas C1 seems to be predominant in patients with EXT1/EXT2-positive sMN). It would be interesting to study the presence of complement proteins depending on the predominant IgG subclass for each individual patient, which could be the reason why there is no difference on the group level, whereas there could be a marked difference on the individual level. No protein from the lectin pathway was analyzed, even though immunostaining of mannose-binding lectin has already been described.8Hayashi N. Okada K. Matsui Y. et al.Glomerular mannose-binding lectin deposition in intrinsic antigen-related membranous nephropathy.Nephrol Dial Transplant. 2018; 33: 832-840Crossref PubMed Scopus (24) Google Scholar The alternative pathway may not trigger but rather maintain complement activation (high detection of complement-regulating proteins of the alternative pathway) (Figure 1), and this requires further investigation. Although the number of patients per group is small and mass spectrometry may have its limitations, especially because the spectral counts were not confirmed by another method (immunostaining or similar), to this date this is nevertheless the most comprehensive analysis of complement proteins, and further studies both in vitro and in vivo are needed to corroborate the results presented and to clarify which pathway is activated at what time in the natural history of MN, following what stimuli and whether the pathway(s) activated may change depending on MN etiology, antigen(s) involved, and the severity of MN. Even though these recent studies suggest somewhat different conclusions, they may nevertheless show that the complement activation is complex and multifactorial and that the 3 pathways are likely redundant in most patients. These articles also open a way to rethink the treatment of patients with MN, which usually consists of immunosuppressive drugs that may be ineffective in approximately 30% of cases, and the patients may relapse in another 30% of cases. For these unresponsive or relapsing patients, especially if their kidney function is rapidly deteriorating, a complement inhibitor may be a valid alternative. A personalized approach based on the individual patient's dominant complement pathway should be considered when possible, and a broad-scale inhibitor targeting a protein downstream of C3 in all other cases. At the moment, several inhibitors of complement are being tested in clinical trials,9Zipfel P.F. Wiech T. Rudnick R. et al.Complement inhibitors in clinical trials for glomerular diseases.Front Immunol. 2019; 10: 2166Crossref PubMed Scopus (29) Google Scholar and their efficacy remains to be determined in comparison with the standard immunosuppressive drugs, such as rituximab. All the authors declared no competing interests. Proteomic Analysis of Complement Proteins in Membranous NephropathyKidney International ReportsVol. 5Issue 5PreviewMembranous nephropathy (MN) is the most common cause of nephrotic syndrome in Caucasian adults. Phospholipase A2 receptor (PLA2R)– and exostosin 1 (EXT1)/exostosin 2 (EXT2)–associated MN represent the most common primary and secondary forms of MN. The complement profile using a proteomics approach has not been studied in these 2 common forms of MN. Full-Text PDF Open Access

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