Immunology of membranous nephropathy: from animal models to humans

Summary

Membranous nephropathy (MN), the leading cause of nephrotic syndrome in adults, is characterized by the deposition of subepithelial immune deposits that consist mainly of immunoglobulin (Ig)G and complement. Most of the cases are primary or idiopathic (iMN), while only approximately 25% of the cases are secondary to some known disease such as systemic lupus erythematosus, hepatitis B, drugs and malignancies. Most of our knowledge on the pathogenesis of iMN has relied upon old experimental models (i.e. Heymann nephritis) that have shown that immune deposits are formed in situ by the reaction of autoantibodies against the respective podocyte antigen. Recent findings indicate that podocyte proteins also act as an autoantigen in human iMN. The M-type phospholipase A2 receptor (PLA2R) has been identified as the main target antigen, as it can be found in approximately 70% of iMN patients but only rarely in other glomerulonephritides. Podocytes damage in the experimental model of Heymann nephritis is complement-mediated. In humans, the presence of complement within the subepithelial deposits is well established, but IgG4, which does not activate complement by classical or alternative pathways, represents the predominant subclass of IgG anti-PLA2R. Some evidence suggests that IgG4 anti-PLA2R autoantibodies can bind mannan-binding lectin (MBL) and activate the lectin complement pathway. A genetic background for iMN has been demonstrated by genome-wide association studies that have shown highly significant associations of the PLA2R1 and the human leucocyte antigen (HLA)-DQA1 loci with iMN. In addition to their diagnostic value, anti-PLA2R antibodies may be useful to monitor disease activity and predict response to treatment.

anti-PLA2R antibody, membranous nephropathy, podocyte, subepithelial deposits IgG4

Introduction

Definition and epidemiology

Membranous nephropathy (MN) is a glomerular disease defined histopathologically by the presence of diffuse thickening of the glomerular capillary wall on light microscopy as a result of an immune complex deposition on the extracapillary side of glomerular basement membrane (GBM). The immune deposits contain the complement fraction C3 and immunoglobulin (Ig)G (mainly IgG4 in idiopathic form) in a peripheral capillary loop pattern, as revealed by immunofluorescence (IF), and appear as electron-dense subepithelial deposits on electron microscopy (EM).

iMN is considered an organ-specific autoimmune disease mediated by autoantibodies, which co-localize with the target antigens to form subepithelial immune complexes (IC), leading to complement activation and the development of proteinuria as a result of podocyte damage.

MN is characterized clinically by non-selective proteinuria, usually in the nephrotic range (>3·5 g/die), and by a possible progression to end-stage renal disease (ESRD).

Idiopathic MN (iMN) accounts for approximately 30% of cases of nephrotic syndrome in the Caucasian adult population (European annual incidence, 1·7 per 100 000), and presents a 2 : 1 male-to-female predominance and a median age of onset from the fourth to the sixth decades [1,2], but the disease can affect patients of all ages and ethnic groups. It is one of the main causes of ESRD among primary glomerulonephritis, and 2% of kidney transplant recipients are affected by iMN as primary renal disease [3].

In developed countries, approximately 75% of all MN are idiopathic (or primary); the remaining 20–25% are secondary to different conditions, such as infections (hepatitis B virus, hepatitis C virus, human immunodeficiency virus, malaria, etc.), malignancies (lung, breast, stomach and ovarian cancer, lymphoproliferative disorder, etc.), systemic autoimmune disease [lupus, rheumatoid arthritis (RA), etc.] and drugs (Table 1).

Table 1

Conditions and drugs associated with membranous nephropathy (secondary forms).

	Common	Uncommon
Immune diseases	Systemic lupus erythematosus	Rheumatoid arthritis, Hashimoto thyroiditis, Sjögren’s syndrome, psoriasis, sarcoidosis, mixed connective tissue disease, IgG4-related disease
Infections	Hepatitis B virus	Hepatitis C virus, streptococcal infection, malaria, Schistosomiasis, syphilis, leprosy
Drugs and toxins	Non-steroidal anti-inflammatory drugs (NSAIDs), gold, penicillamine	Captopril, clopidogrel, mercury
Tumours	Cancers (bladder, breast, pancreas, prostate, stomach, lung)	Lymphomas, chronic lymphocytic leukaemia
Miscellaneous	Diabetes mellitus, renal transplantation	Sickle cell disease, haematopoietic stem cells transplantation

Pathological and clinical features

Diagnosis of both primary and secondary membranous nephropathy relies on renal biopsy, in particular on the finding of deposits of IgG in a granular pattern along the glomerular capillary loop by IF (Fig. 1), particularly in the earliest stage (I) in which the glomeruli may appear normal on light microscopy [4].

Fig. 1

Granular subepithelial deposits of immunoglobulin (Ig)G in a case of idiopathic membranous nephropathy (original magnification ×400).

In the next stages (II–IV) there is a progressive homogeneous thickening of the capillary wall, with the formation of projections of the GBM between deposits called ‘spikes’, until the last stage (V) in which the deposits are not recognizable as they are completely incorporated into the GBM [5].

Some histological features may help in discrimination between the two forms of MN (Table 2).

Table 2

Distinctive histopathological features of secondary forms of membranous nephropathy.

	Features
Light microscopy	Significant mesangial proliferation
Immunofluorescence	• Positive staining for IgG1 or IgG3, IgA, IgM   • Positive staining for C1q and/or C4   • Mesangial immunofluorescence deposition
Electron microscopy	Electron-dense deposits in mesangial and/or subendothelial sites

Ig: immunoglobulin.

In primary MN, no endocapillary proliferation is usually seen, and the presence of a pronounced mesangial proliferation implies a secondary form of MN.

IgG4 is predominant for unknown reasons in idiopathic MN. A positive staining for non-IgG4 subclasses (IgG1, IgG3), IgA, IgM or significant staining in the glomerular mesangium suggests a secondary MN, often lupus nephritis class V.

Complement component C3 is also present in approximately 50% of iMN patients, and its presence probably reflects active, ongoing immune deposit formation and complement activation [6].

C4 and C1q, expression of a complement activation through the ‘classical pathway’, are often absent in iMN and their presence is suggestive of secondary membranous nephropathy.

On electron microscopy, the hallmark lesions are subepithelial electron-dense deposits, effacement of the foot processes and expansion of the glomerular basement membrane due to deposition of new extracellular matrix between the deposits. The electron-dense deposits reflect the IgG and C3 staining on IF, so in idiopathic form they are not usually seen at subendothelial or mesangial level.

Despite the characteristics described, discrimination between the two forms of MN can sometimes be extremely challenging.

With disease progression, especially in severe proteinuric cases, focal glomerular segmental sclerosis and interstitial tubular damage is observed [7].

iMN is a chronic disease with a variable and unpredictable clinical outcome, which can include spontaneous remissions and relapses. Spontaneous remission occurs in up to 30–40% of cases [8]; the remaining two-thirds of the patients present with persistent proteinuria, and approximately 40% of those will progress within 10 years to ESRD [9]. Consequently, treatment with potentially toxic drugs remains controversial. However, an increase of cardiovascular risk, hypercoagulability, major susceptibility to infections and progressive renal failure afflict a severe and persistent nephrotic syndrome.

The identification of reliable prognostic factors (clinical, laboratoristic and/or histological) is extremely important to guide any therapeutic decision. Classical predictors of long-term progression are baseline proteinuria more than 8 g/day, male sex, important tubular-interstitial damage and glomerular sclerosis at renal biopsy, age older than 50 years and altered renal function at onset [10].

Achieving complete remission predicts an excellent long-term renal prognosis and those patients have an almost 100% renal survival at 10 years, whereas the number falls to 90% with partial remission and 45% with no remission [11].

Pathogenesis

From experimental models to identification of human antigenic targets

iMN is an excellent example of disease in which most of the knowledge on the pathophysiological mechanisms is derived from animal experimental studies; in particular, the model of Heymann nephritis [12], which allowed identification of the podocyte target antigen of the autoantibody response in rats and showed that the formation of the IC occurs in situ.

In theory, subepithelial IC deposits can form in three different ways. Antibodies can bind to exogenous antigens that localize on the subepithelial surface because of their cationic charge and small size (Fig. 2); secondly, antigens and antibodies can be trapped as immune complexes on the glomerular filtration wall (Fig. 3); and finally, the antigens could be endogenous constituents of a fixed subepithelial structure, such as a podocyte membrane protein (Fig. 4) [13].

Fig. 2

Mechanism of in-situ subepithelial immune complex formation in early childhood idiopathic membranous nephropathy. Because of its size and charge, modified, the cationic form of bovine serum albumin (BSA) reaches anionic glomerular subepithelial structures and serves as a planted antigen with subsequent formation of immune complexes in situ. The functional impairment represented by proteinuria is the result of formation of the membrane attack complex (C5b-C9, MAC), which leads to sublethal podocyte injury resulting in the activation of transcription factors encoding for mediators of fibrosis and cytoskeletal podocyte rearrangement. It also increases production of potentially nephritogenic molecules such as reactive oxygen species (ROS), proinflammatory cytokines, proteases and vasoactive molecules.

Fig. 3

Mechanism of circulating immune complex deposition in membranous nephropathy. Preformed small-sized circulating immune complexes may traverse the glomerular basement membrane (GBM) and deposit beneath the podocyte. The functional impairment represented by proteinuria is the result of formation of the membrane attack complex (C5b-C9, MAC), which leads to sublethal podocyte injury resulting in the activation of transcription factors encoding for mediators of fibrosis and cytoskeletal podocyte rearrangement. It also increases production of potentially nephritogenic molecules such as reactive oxygen species (ROS), proinflammatory cytokines, proteases and vasoactive molecules.

Fig. 4

Mechanism of anti-podocyte autoantibody-mediated disease in membranous nephropathy. Circulating autoantibodies can target surface-exposed intrinsic podocyte proteins to form in-situ immune deposits. The functional impairment represented by proteinuria is the result of formation of the membrane attack complex (C5b-C9, MAC), which leads to sublethal podocyte injury resulting in the activation of transcription factors encoding for mediators of fibrosis and cytoskeletal podocyte rearrangement. It also increases production of potentially nephritogenic molecules such as reactive oxygen species (ROS), proinflammatory cytokines, proteases and vasoactive molecules.

In the experimental rat model of Heymann nephritis, the subepithelial deposits are formed in situ when circulating antibodies (resulting from either active or passive immunization of the animal) bind an intrinsic antigen in the glomerular capillary wall. This antigen was identified as megalin, a glycoprotein of 516 kDa members of the low-density lipoprotein (LDL) receptor family present, expressed with clathrin, on the foot process of podocytes [14,15,16,17].

The binding of circulating anti-megalin antibodies to surface megalin induces complement activation and local generation of the membrane attack complex (MAC, C5b-C9). The immune complexes are subsequently degraded and form discontinuous subepithelial deposits.

The functional impairment represented by proteinuria is the result of the formation of MAC, which leads to sublethal podocyte injury resulting in the activation of transcription factors encoding for mediators of fibrosis and cytoskeletal podocyte rearrangement. It also increases the production of potentially nephritogenic molecules such as reactive oxygen species (ROS), proinflammatory cytokines, proteases and vasoactive molecules (Fig. 4) [13,18].

However, megalin is absent in human glomeruli and its human counterpart, the LDL receptor, is not detected in the subepithelial immune deposits of iMN patients [19].

A fundamental step in the identification of antigens involved in human iMN was the discovery by Ronco et al., in 2002, of a human counterpart to passive Heymann nephritis in a neonate born with membranous nephropathy. Maternal antibodies to neutral endopeptidase (NEP), which crossed the placenta and bound to fetal glomerular podocytes, induced the disease antenatally [20,21]. The mother was a carrier of a homozygous deletion in the gene encoding the protein NEP and became alloimmunized to the paternally inherited neutral endopeptidase antigen expressed in the placenta.

This rare form of MN was also the first demonstration of the cardinal role of circulating antibodies against intrinsic podocyte antigens in the pathogenesis of human disease, and the detection of MAC C5b-C9 in the subepithelial deposits confirmed that the role of complement was also central in human MN.

In 2011, Debiec et al. described another rare form of early childhood MN in which a modified, cationic form of bovine serum albumin (BSA), derived probably from dietary sources and absorbed intact by the immature intestinal tract of infants, served as a planted antigen. The size and charge of this exogenous antigen are responsible for its localization at the glomerular filtration barrier, binding to anionic glomerular structures and the subsequent formation of immune complexes in situ (Fig. 2) [22].

Both NEP and megalin were ruled out as potential antigens in adult idiopathic MN, but recent evidence indicates that the majority of patients with primary MN have circulating autoantibodies to the M-type phospholipase A2 receptor 1 (PLA₂R) [23].

The major human target in iMN: M-type PLA₂R

In 2009, Beck et al. demonstrated the presence of circulating anti-PLA2R antibodies in 26 of 37 iMN patients, performing Western blotting under non-reducing conditions with extracts from normal human glomeruli as a source of antigens. They observed a high-molecular-weight band which, after partial purification using lectin chromatography, resulted in the mass spectrometric identification of PLA2R, a protein expressed in the podocytes.

Such anti-PLA2R antibodies were highly specific for idiopathic forms as they were not detected in sera of controls, patients affected by other primary glomerulonephritis or by secondary forms of MN. Circulating anti-PLA2R antibodies of patients with primary iMN were predominantly, but not exclusively, IgG4. The receptor of PLA2 and IgG4 co-localized in the immune deposits at subepithelial level, and only the IgG eluted from the biopsy samples of iMN patients reacted with the PLA2R. These results led to the confirmation that the pathogenic mechanisms underlining human iMN were similar to the one responsible of the Heymann nephritis [23].

Circulating autoantibodies to PLA2R were detected in approximately 70% of patient with iMN in all the different studies performed.

PLA2R is a transmembrane glycoprotein of highly glycosylated 185 kDa, and is a member of the mannose receptor (MR) family. All MR family members have a conserved extracellular structure, with an N-terminal cysteine-rich domain (Cys-R), a fibronectin II-like domain (FNII) and eight to 10 C-type lectin-like domains (CTLD) [24]. The cytoplasmic domain is short and contains motifs important for the constitutive recycling of these receptors, as all members are internalized with their ligands and recirculate continuously between the membrane and the endosomal compartment. MR family members undergo conformational shifts between a more extended conformation and a compact, folded configuration that may be regulated by pH, oligomerization and/or ligand binding [25]. This conformational shift is particularly important, because the target epitopes of the circulating autoantibodies appear to be accessible only in one of the two conformations.

Studies of the different reactivity of iMN patients’ sera to the native and deglycosylated forms of PLA2R show that the autoantibodies recognize a conformational epitope, and studies of high-throughput capture immunoassay allowed the identification of putative linear epitopes [26].

In 2015, a major immunodominant epitope region was characterized in the three most N-terminal domains of PLA2R by US [27] and British groups [28], who each used different technical approaches. Two major overlapping epitopes have been identified. The first, characterized by Western blotting of truncated extracellular domains of PLA2R under non-reducing conditions, is a protein complex consisting of the Cys-R domain, the FNII domain and the CTLD domain 1 of PLA2R [27]. Absence of either the Cys-R or the CTLD1 domain prevents autoantibody recognition of the remaining domains. This three-domain complex contains at least one disulphide bond (required for conformational configuration) and completely blocks the reactivity of autoantibodies with the full length PLA2R.

The second overlapping epitope was identified in the Cys-R domain. Two peptides from the Cys-R domain showed strong inhibition of autoantibody binding to PLA2R by surface plasmon resonance, with a sequence covering both peptides (31-mer) producing 85% inhibition of autoantibody binding. Anti-PLA2R antibody directly binds this 31-mer peptide under non-denaturing conditions, and binding is sensitive to reduction because of an internal disulphide bond [28]. The identification of these major PLA₂R epitopes could enable future therapeutic strategies for iMN patients, including antibody inhibition therapy and immunoadsorption.

The physiological role of PLA2 receptor is unclear. Binding of circulating PLA2 to its receptor participates in both positive and negative regulation of PLA2 functions as well as in its clearance by internalization (endocytosis) of ligand–receptor complex. PLA2R also regulates cellular senescence through the production of ROS and the activation of the DNA-damage pathways [29].

PLA2R is expressed highly in kidney tissue and is confined almost exclusively to the glomerular podocytes [30].

Predisposing gene variation for idiopathic MN

Apart from rare cases, MN is not a typical hereditary disease in Mendelian terms [31]. However, the influence of genetic factors is well established in both rats and humans.

Genome-wide association studies have shown highly significant associations of the 6p21 HLA-DQA1 and 2q24 PLA2R1 loci with idiopathic membranous nephropathy in Caucasian European patients. These risk alleles of the two genes had an additive effect for development of idiopathic membranous nephropathy. Patients carrying all four risk alleles had an odds ratio close to 80, compared with individuals who had only the protective alleles [32].

The observation that anti-PLA2R antibodies were found in 73% of patients with high-risk genotypical variations, while they were absent in non-carriers, supports the role of PLA2R as a principal antigenic target in iMN [33]. Additional studies are needed to explain how alleles in the PLA2R1 and HLA-DQA1 loci interact with each other to increase susceptibility to membranous nephropathy.

A possible explanation is that a particular HLA molecule may facilitate the autoimmune response against PLA2R presenting it to T helper type 2 in an aberrant or exuberant way [34].

Additional candidate antigens

Using a proteomic approach involving the use of in-vitro human podocytes exposed to iMN patient sera, in 2012 Ghiggeri et al. identified various intracellular enzymes [superoxide dismutase 2 (SOD2) aldose reductase AR and α-enolase] as different targets of circulating autoantibodies in MN [35]. These antigens co-localize in iMN patient biopsies with MAC C5b-9 and IgG4, but they are not normally expressed highly in normal glomeruli and are not present on the cell surface of podocytes. It is possible that podocyte over-expression and delocalization of SOD2, and AR may represent an anti-oxidant response preceding the humoral immune response [35]. These characteristics suggest that they are more likely to be neo-antigens exposed aberrantly on cellular surface after the initial podocyte damage, with the consequent production of autoantibodies that could worsen and/or maintain the podocytes complement-mediated damage [36]. In Heymann nephritis, podocyte-produced oxygen radicals in the presence of C5b-9 and mediate glomerular damage. In this light, anti-SOD2 and anti-AR antibodies should follow a first autoimmune phase [35].

The prevalence of anti-SOD2, anti-AR and anti α-enolase antibodies in iMN is lower than that of anti-PLA2R, reaching values of 28, 34 and 43%, respectively, and their specificity appears not comparable to anti-PLA2R antibodies as they are also present in other autoimmune diseases [anti-SOD2 in systemic lupus erythematosus (SLE), anti α-enolase in SLE and RA] [35]. Although no strong association with clinical outcome was found for any single autoantibody, follow-up proteinuria was lower in patients who were negative for all antibodies [35].

In 2014 Tomas and Beck discovered the presence of circulating autoantibodies against THSD7A (thrombospondin type-1 domain containing 7A), a protein of 250 kD glomerular, in 8–14% of iMN patients’ sera negative for anti-PLA2R. This protein shares different biochemical characteristics with PLA2R, such as N-glycosylation, transmembrane localization in glomerular podocytes and serum reactivity only in non-reducing conditions [37].

Anti-THSD7A antibodies also appear specific, as they are not detected in healthy individual serum, in patients with secondary MN or different glomerulopathy. Interestingly, these antibodies are mutually exclusive with anti-PLA2R, suggesting that PLA2R-associated and THSD7A-associated MN are two separate molecular entities [37].

Further additional non-identified autoantigens might exist, as 10–20% of serum samples from iMN patients are negative for both anti-PLA2R and THSD7A antibodies.

Disease effectors: differences between PLA2R-associated iMN and Heymann nephritis

Podocyte damage in the Heymann nephritis experimental model is complement-mediated, as established by the presence of C5b-9 in the subepithelial deposits and the lack of proteinuria development, with the final depletion of complement-cascade components or the use of anti-megalin antibodies inhibiting complement activation [38].

In human disease, the presence of complement factors within the subepithelial deposits is well established, but IgG4, which does not activate complement by classical or alternative pathways, represents the predominant subclass of IgG anti-PLA2R.

The discrepancy could have two different explanations. The first is based on the observation that both IgG1 and C1q are detected especially in early immune deposits [39], and there are low levels of circulating IgG1 or IgG3 anti-PLA2R [23] which could, possibly, be responsible for complement activation through the classical pathway.

The second more probable explanation could be that IgG4 anti-PLA2R autoantibodies can bind mannan-binding lectin (MBL) and activate the lectin complement pathway. Purified anti-PLA2R IgG4 autoantibodies from iMN patients have a high ratio of GalNAC (N-acetylglucosamine) to Gal in a terminal position, an amino acidic sequence not usually present in mammalian carbohydrates, and thereby can bind to C4 through MBL in vitro [40].

In addition to activating complement, anti-podocyte antibodies might directly change podocyte biology. Soluble PLA2 (sPLa2R) is a potent proinflammatory enzyme. Binding of sPLA2 to its receptor regulates its function positively and negatively depending on the cell type. PLA2R could act as a clearance receptor with potentially anti-inflammatory activity, which might be affected by an anti-PLA2R antibody. PLA2R also regulates cellular senescence, and because markers of senescence are over-expressed in podocytes from patients with iMN, a potential agonistic activity of anti-PLA2R antibodies should be considered [41].

Anti-PLA2R antibodies

A few years after the discovery of the role of anti-PLA2R antibodies in iMN, many studies on their prevalence and clinical significance have been published. Anti-PLA2R autoantibodies have emerged as a specific and sensitive biomarker of idiopathic membranous nephropathy.

There are at least two commercially available tests for the detection and quantification of circulating anti-PLA2R antibodies (Euroimmun AG, Lübeck, Germany). The immunofluorescence test, which provides a qualitative and semiquantitative antibody analysis, uses biochips coated with human embryonic kidney cells (HEK293) transfected (or not, to serve as negative control) with the full-length human PLA2R1 cDNA and incubated with a serum sample from the patient [42]. The enzyme-linked immunosorbent assay (ELISA), based on purified recombinant PLA2R, enables a more quantitative and faster identification of anti-PLA2R than the immunofluorescence test, although the latter is slightly more sensitive [43]. As the specificity of these tests for iMN is close to 100%, some authors suggest not performing a renal biopsy in selected cases (elderly, single kidney or coagulation disorders) if the PLA2R test is positive [44]. The sensitivity is, instead, approximately 70–80% in all the population studies carried out to date.

A low prevalence of anti-PLA2R antibodies is reported in a secondary form of MN related to infection, drug intoxication, graft-versus-host disease and tumours, in which it can be difficult to exclude a correlation of iMN with the associated disease [45,46,47,48]. In addition, patients with MN related to sarcoidosis or active hepatitis B may show an increased prevalence of anti-PLA2R antibodies, which suggests that immunological disorders associated with these two diseases might induce or enhance immune response against PLA2R [48,49].

Detection of the PLA2R antigen in immune deposits in biopsy speciments is also possible with the use of a commercial antibody after a retrieval step to unmask PLA2R epitopes [50]. This method appears to be more sensitive than the detection of circulating antibodies, as the PLA2R antigen can still also be found in deposits in some anti-PLA2R seronegative patients. Several explanations could be proposed, including the possible rapid clearance of circulating antibodies, immunological remission or kidney biopsy performed long after disease onset. In addition, this method allows the retrospective diagnosis of PLA2R-related MN in archival kidney biopsy samples, especially in patients awaiting a kidney graft, because of the possibility of a recurrence of the primitive disease on the transplanted kidney. Although the detection of PLA2R antigen in biopsy specimens is promising, the measurements of circulating antibodies appear more accessible and simpler to perform.

Anti-PLA2R antibodies: clinical applications

In addition to the diagnostic significance of the PLA2R antibodies, many studies have shown a correlation between the concentration of circulating antibodies and disease activity expressed in terms of urinary protein output. Anti-PLA2R antibodies usually become undetectable at spontaneous or treatment-induced remission and re-emerge or increase at relapse [23,51,52,53,54].

Anti-PLA2R antibody concentration also seems to predict outcome, as high serum levels correlate with a lower probability of spontaneous or treatment-induced remission and with an increased risk of deterioration in renal function. The time intervals from the start of immunosuppressive therapy to remission are increased in patients with the highest antibody titres [53–56].

Several studies have shown that partial or complete depletion of anti-PLA2R antibodies precedes renal remission by several weeks or months [51]. The time lag from immunological remission to renal remission probably corresponds to the time required for the restoration of the glomerular filtration barrier. Monitoring of anti-PLA2R titres could also be relevant in cases of partial remission in which the persistent proteinuria might be due to immunological activity or irreversible podocyte damage, in which a continuation of immunosuppressive therapy would have no benefit.

Furthermore, antibody titres at the end of immunosuppressive treatment seem to predict recurrences, as relapses are observed more frequently in patients with high antibody titres after treatment [57] (Table 3).

Table 3

Clinical value of anti-phospholipase A2 receptor (PLA2r) antibodies.

	Features
Diagnostic biomarker	High specificity Good sensitivity
Prognostic biomarker	High serum titres correlate with:   Lower probability of reaching clinical remission or longer time to reach it Higher rate of recurrence
Monitoring tool	Serum titres correlate with immunological disease activity Adjustment of immunosuppressive treatment based on immunological activity to limit side effects

Quantification of anti-PLA2R antibodies is becoming a monitoring tool of immunological activity of idiopathic membranous nephropathy; however, further studies on larger cohorts of patients are needed to establish and confirm their real utility value in clinical practice.

Disclosure

Authors have no competing interests to disclose.