Type and precursor protein of amyloid nephropathy.
Amyloidosis comprises a group of protein-folding disorders in which extracellular deposits share unique Congo red staining properties and fibrillary ultrastructural appearance. These fibrillary deposits ultimately cause tissue destruction and progressive disease. Amyloidosis can be either systemic affecting multiple organs or localized. Renal involvement by amyloidosis (amyloid nephropathy) is a frequent manifestation of systemic amyloidosis. Immunofluorescence, immunohistochemistry (IHC), and more recently laser microdissection and mass spectrometry (LMD/MS) are important techniques in typing of amyloid nephropathy. This in-depth review discusses practical diagnostic approach and pathogenesis of amyloid nephropathy and includes discussion of treatment and prognosis.
- amyloid nephropathy
- light microscopy
- electron microscopy
Amyloidosis comprises a group of protein-folding disorders in which extracellular deposits share unique Congo red staining properties and fibrillary ultrastructural appearance . These fibrillary deposits ultimately cause tissue destruction and progressive disease. Amyloid consists of randomly arranged, nonbranching fibrils that measure 8–12 nm in diameter . Amyloidosis is a rare group of diseases, with an estimated prevalence of 1: 60,000 . In the USA and Europe, amyloidosis derived from immunoglobulin (Ig) light chain (AL) secondary to plasma cell dyscrasia is the most prevalent form, followed by reactive AA amyloidosis (AA) derived from serum amyloid A (SAA), which is typically associated with chronic inflammatory conditions. This is in contrast to developing countries in Africa and Middle East of Asia, where AA is much more common than AL [3–5]. Leukocyte chemotactic factor 2 amyloidosis (ALECT2), derived from leukocyte chemotactic factor 2 protein (LECT2), is newly recognized as a common type of amyloid, with unknown etiology . Familial amyloidosis is diagnosed with increasing frequency with the use of new immunohistochemical studies and mass spectrometry . Amyloidosis can be either systemic affecting multiple organs or localized. Renal disease is a frequent manifestation of systemic amyloidosis with AL, previously called primary amyloidosis, the most common type involving the kidney.
2. Amyloid nephropathy
The types of amyloid are categorized by the chemical composition of the proteins. There are more than 25 precursor proteins identified as major proteins in amyloid deposition so far. A large study from the Mayo clinic  showed that among 474 patients with amyloid diagnosed by renal biopsies between 2007 and 2011, Ig-related amyloidosis (AIg) was the most common form involving the kidney (85.9%), followed by AA (7.0%), ALECT2 (2.7%), fibrinogen A α chain amyloidosis (AFib) (1.3%), apolipoprotein AI amyloidosis (AApo AI), apolipoprotein AII amyloidosis (AApo AII), or apolipoprotein AIV amyloidosis (AApo AIV) (0.6%), AA/light and heavy chain amyloidosis (AHL) (0.2%), and unclassified amyloidosis (2.3%). AIg in most cases is derived from fragments of monoclonal light-chain protein (AL). However, in rare cases, AIg is derived from truncated Ig heavy chain and light chain (AHL) or isolated truncated Ig heavy chain [8, 9]. AIg is associated with B-cell lymphoproliferative disorders including multiple myeloma and plasma cell dyscrasia, B-cell lymphoma, and Waldenström’s macroglobulinemia . In contrast, AA is characterized by tissue deposition of serum amyloid A protein, which is derived from an acute-phase reactant protein synthesized by the liver . AA is seen in conditions associated with chronic inflammation including rheumatoid arthritis, ankylosing spondylitis, chronic draining infections (i.e., osteomyelitis, chronic skin infections including decubitus ulcers, bronchiectasis, and chronic sinusitis), Crohn disease, tuberculosis, and familial Mediterranean fever (FMF) . Familial amyloidosis comprises another group of amyloid that is now being diagnosed more frequently and includes amyloid derived from transthyretins (TTR) , fibrinogen , lysozyme (Lys) , gelsolin (Gel) , Apo AI , Apo AII , and Apo AIV . ALECT2 nephropathy was first described in 2008 [6, 18]. LECT2 is a chemotactic factor for neutrophils and has other physiologic functions, including cell proliferation, immunomodulation, repair after injury, tumor suppression, and glucose metabolism [6, 18]. ALECT2 is now the third most common type of amyloid nephropathy in the USA and accounts for 2.5–2.7% of amyloid nephropathy cases [6, 18]. ALECT2 involves mainly in the kidney and liver but rarely involve other organs such as spleen, adrenal, and myocardium [6, 18]. Type and precursor protein of amyloid nephropathy are summarized in Table 1.
|Amyloid precursor protein||Amyloid type|
|Restricted light chain (lambda or kappa)||AL|
|Ig heavy chain||AH|
|Ig heavy and light chain||AHL|
|Serum amyloid associated protein (SAA)||AA|
|Leukocyte chemotactic factor type 2 (LECT2)||ALECT2|
|Fibrinogen A-α chain||AFib|
|Apolipoprotein A-I||AApo AI|
|Apolipoprotein A-II||AApo AII|
|Apolipoprotein A-IV||AApo AIV|
3. Clinical features
The clinical features of patients with amyloidosis vary, depending on the varying predilection of different types of amyloid for specific organ involvement. As described above, renal involvement is a frequent manifestation of amyloidosis, more often in AIg nephropathy, AA nephropathy, and some forms of familial amyloidosis [10, 12]. Amyloid nephropathy of any type is more common in men than in women . A large retrospective review of patients with amyloidosis evaluated from 1981 to 1992 at the Mayo Clinic in Rochester, Minnesota, revealed 1315 patients, including 918 patients with AL amyloidosis (69.8%). Of these, 474 patients had new-onset AL amyloidosis, including 69% men and 31% women with median age of 64 years . At the time of diagnosis, about 17% of AL patients had either multiple myeloma or smoldering myeloma and about 16% had history of monoclonal gammopathy of undetermined significance (MGUS). On presentation, about 51% of men and 47% of women had renal failure, and about 73% of patients had proteinuria. The median 24-h urine protein was 1.2 g/d and in the patients with full nephrotic syndrome, about a quarter of patients, the mean 24-h urine protein excretion was 7.0 g/d. Serum protein electrophoresis (SPEP) revealed a monoclonal protein in about 48% of patients and when serum immunoelectrophoresis was tested the percentage increased to about 72%. A monoclonal light chain was detected in about 73% of the patients by urine immunoelectrophoresis or immunofixation, including about 68% with lambda and about 32% with kappa. Overall, about 89% of the patients with AL amyloidosis showed a serum or urine monoclonal spike (M spike).
Patients with AA nephropathy usually present at younger age than AL patients, whereas ALECT2 is more common in older patients. ALECT2 nephropathy mainly affects patients of Hispanic or Mexican origin and rarely affects Caucasian patients, whereas AL and AA do not show evident ethnic differences [6, 18]. As in AL amyloid, proteinuria is also the most common clinical presentation in AA, ALECT2, and familial amyloid nephropathy . Extrarenal manifestations of amyloidosis include congestive heart failure caused by myocardial infiltration by amyloid, orthostatic hypotension, bladder dysfunction, and dysesthesias caused by amyloid infiltration into autonomic and peripheral nerves, lymphadenopathy, hepatomegaly, splenomegaly, and macroglossia [18, 20]. The treatment and prognosis of amyloid nephropathy will be discussed below.
4. Molecular mechanisms and pathogenesis of amyloidosis
Misfolding of extracellular proteins has a prominent role in the molecular mechanisms and pathogenesis of amyloidosis [21, 22]. The misfolded proteins are highly prone to self-aggregation. There are different mechanisms of formation of pathologic misfolded proteins . The first is based on intrinsic propensity of the protein to assume pathologic conformation, which becomes more evident with aging. Examples of these mechanisms are evident when molecularly normal transthyretin misfolds in patients with senile systemic amyloidosis . The second way is due to alteration of the normal protein sequence, as seen with the replacement of a single amino acid in protein, e.g., in AL and familial amyloidosis . Only a small portion of Ig light chains is amyloidogenic; thus, AL nephropathy occurs only in about 12–15% of the patients with multiple myeloma . The amyloid fibrils in amyloid nephropathy consist of either intact light chains containing the variable and constant domains or solely the variable domains, which contains the N-terminus portion of the light-chain molecule. The VλVI subgroup of the light chain preferentially leads to amyloid formation in patients with AL nephropathy [23, 24]. Therefore, it appears that germ line sequences, which enhanced near the N-terminus of the lambda light chain and in the VλVI of the light chain may be prone to mutations that generate amyloidogenic light chains. These altered proteins lead to destabilization of light chain and increase the likelihood of fibril formation . In familial amyloidosis, such as Transthyretin-related hereditary amyloidosis (ATTR) and Lysozyme-related amyloidosis (ALys), the substitution of a single amino acid transforms a normal protein into an amyloidogenic protein [26, 27]. The unstable protein produced by amino acid substitution may allow the protein to precipitate when stimulated by the local physicochemical milieu, such as local surface pH, electric field, and hydration forces on the cellular surfaces . A third mechanism contributing to amyloid formation is proteolytic remodeling of the protein precursor, as seen in Alzheimer’s disease, in which the fibrils are composed of proteolytic fragments of 39–43 residues derived from 753-residue β-amyloid precursor protein (APP) . This type of amyloid does not affect the kidney. In addition, excessive concentration of amyloidogenic protein due to unregulated production of high local concentration can promote amyloidosis . When the protein precursor reaches a critical point of local concentration, it triggers fibril formation. This mechanism is enhanced further by environmental physicochemical factors and interaction with extracellular matrix. This mechanism may occur in AA amyloidosis associated with chronic inflammatory conditions or familial Mediterranean fever . The excessive concentration of amyloidogenic protein may also be caused by decrease in clearance from the body; e.g., Beta-2 microglobulin associated amyloidosis (Aβ2M) develops in end-stage renal disease patients who received long-term dialysis because of ineffective clearance of β2M from circulation during dialysis or due to inability of the body to destroy the accumulation by natural mechanism . Regardless of mechanism of misfolding, the misfolded proteins are prone to self-aggregate, generating protofilaments that interact to form fibrils .
In AL nephropathy, amyloid formation in the kidney first begins in the mesangium. The specific uptake of light-chain protein by mesangial cells underlies the predominant kidney tropism and is an important step in amyloid fibril formation. There are several factors that might promote or decelerate amyloid deposition in glomeruli, including the negative ion charge and the high concentration of glycosaminoglycan of the glomerular basement membranes with the presence of enzyme proteases that could render protein amyloidogenic . Mesangial cells are modified smooth muscle cells, which have phagocytic activity . Upon interaction with light-chain proteins, the light-chain proteins are avidly internalized and delivered to the primary lysosomes where the amyloid fibrils are primarily formed . During this process, the mesangial cells transform into a macrophage phenotype with prominent primary lysosomes, making them more capable of processing of internalized amyloidogenic light-chain proteins and fibril formation . The amyloid deposition within the mesangium further stimulates metalloproteinase enzymes, causing mesangial matrix degradation, inhibiting transforming growth factor β (TGF-β) and thus impairing mesangial matrix repair [33, 35] and increasing apoptosis, finally leading to significant mesangiolysis and replacement of the mesangial area by amyloid deposits . These changes result in the absence of mesangial argyrophilia and significant mesangial cell deletion in the advanced stage of glomerular amyloidosis .
LECT2 has multiple functions including as a cytokine involved in chemotaxis of neutrophils and a growth factor involved in cell proliferation and regulation of repair after injury, immunomodulation, tumor suppression, and glucose metabolism . The pathogenesis of ALECT2 is not well understood, but may be due to increased synthesis of LECT2 by hepatocytes or secondary to hepatocellular damage or involve interference, possible due to genetic defect, in the LECT2 catabolism or LECT2 transportation, which may give rise to local LECT2 tissue concentration and finally lead to amyloid fibril formation [6, 18, 37].
The normal plasma protein serum amyloid P component (SAP), a glycoprotein that belongs to the pentraxin family, independently binds to fibrils in all types of amyloid and contributes to pathogenesis of amyloidosis . SAP is highly protected against proteolysis, and a binding of SAP to amyloid fibrils in vitro protect them from proteolytic enzymes and degradation by phagocytic cells. Moreover, SAP is a stubborn glycoprotein that can persist within human amyloid deposits for prolonged periods and is completely unmodified with respect to circulating SAP . It is suggested that SAP may contribute to the failure to clear amyloid deposition in vivo, leading to tissue architecture destruction and organ dysfunction.
Furthermore, amyloid can be deposited in multiple organs, and this tendency might depend on several physicochemical factors, such as high concentration of local protein, low pH, presence of proteolytic processing, and seeding of protofilaments . The amyloid deposits cause tissue architecture destruction, presumed to cause organ dysfunction . Furthermore, the amyloidogenic precursor proteins, folding intermediates, and protofilaments have toxicities independent of the amyloid deposits and these toxicities can also contribute to disease manifestations .
5. Gross findings
Postmortem examination of patients with amyloidosis generally shows enlarged kidneys, unlike other causes of chronic kidney disease (CKD) where kidneys are small and shrunken. In addition, cut surfaces of kidney in patients with amyloid nephropathy are pale, firm, waxy, and flat  (Figure 1a), which are different from the normal kidney or the kidney in the patients with CKD (Figure 1b), which bulges slightly causing in slight curvature of the cut surfaces.
6. Histologic diagnosis and identification of amyloid
6.1. Light microscopy
The light microscopic (LM) findings of amyloidosis are identical regardless of the type of amyloid. Glomerular amyloid deposition begins with progressive accumulation of acellular amorphous eosinophilic material (cotton candy appearance) on hematoxylin and eosin (H&E)-stained sections (Figure 2) that appear pale with the periodic acid Schiff (PAS) stain (Figure 3a and b). In the advanced stage, the mesangial matrix is extensively replaced by acellular amorphous material exhibiting uniform expansion with compression of the capillary spaces and occasional nodular formation, resembling diabetic nephropathy or monoclonal immunoglobulin deposition disease. The nodular pattern is seen more frequently in AA nephropathy. The amyloid deposits are paler on PAS stain than the Kimmelstiel-Wilson nodules in diabetic nephropathy, or deposits in light-chain deposition disease or fibrillary glomerulonephritis. Further, fibrillary glomerulonephritis typically is proliferative, with increased cellularity seen by light microscopy. The amyloid deposits stain weakly or are negative with Jones methenamine silver stain (JMS) and appear as negative defects in the expanded mesangium and thick glomerular basement membranes (Figure 4a and b). Occasionally, there is a focal parallel alignment of amyloid fibrils in the subepithelial zone that results in focal capillary wall spikes, which are best visualized by JMS (Figure 5). These spikes are focal, closely clustered, and longer than the typical spikes of membranous nephropathy. The focal clusters of spikes may resemble feathers, so-called feathery spikes. Amyloid feathery spikes are more common in AL than AA or familial amyloidosis . Rarely crescent formation can be seen in both AA and AL , indicating glomerular basement membrane breaks, the injury that triggers crescent formation, can occur. Vascular involvement by amyloidosis is common, frequently involving arteriolar walls, followed by arteries, peritubular capillaries, and veins. In rare cases, particularly in AL or in ATTR nephropathy, the vessels are the only part in the kidney where amyloid is demonstrated. Interstitial amyloid deposition is seen in about 50% of cases but is present in most cases of ALECT2 nephropathy (Figure 6). Glomerular involvement is not extensive in ALECT2 and apolipoprotein AI (AApo AI/), AII (AApoAII), and AIV (AApoAIV) nephropathy in comparison with other types of amyloid. In addition, the histology of AFib nephropathy is very characteristic, showing glomerular enlargement with near-total replacement of the glomeruli by amyloid, with little or no vascular or interstitial involvement . Special IF and immunohistochemistry (IHC) together with mass spectrometry analyses are typically used to identify the type of amyloid (see below). However, potassium permanganate treatment prior to Congo red staining has been used to distinguish between AA and AL nephropathy: after this treatment, birefringent Congo red staining is lost by AA but retained by AL. This technique is not commonly used and has been replaced by more specific SAA immunohistochemistry (IHC).
Amyloid is defined by its tinctorial characteristics, which include Congo red positivity (orange, salmon pink, or pale rose staining, Figure 7). The Congo red stain gives apple-green or traffic light green birefringence under polarized light (Figure 8). The mesangial expansion can be focal and may be segmental, global, or even nodular. However, the degree of proteinuria does not correlate with the amount of amyloid deposition; as a result, cases with early amyloidosis with scant and segmental amyloid deposition can be mistakenly diagnosed as minimal change disease if no Congo red stain, immunofluorescence (IF) and electron microscopy (EM) is performed. To demonstrate small amounts of amyloid deposits in tissue sections, it is recommended that the sections be cut thicker than normal (6 μm, instead of customary 2 μm) . Proper detection of apple green birefringence depends on the intensity of the transmitted light and, thus, a strong light source is strongly suggested to maximize results. In early amyloidosis with small amounts of amyloid, it might be difficult to demonstrate Congo red positivity. Therefore, an alternative way of identifying a small amount of amyloid deposits by Congo red stain is to place the stained section under fluorescent light; amyloid then is bright red  (Figure 9). Of note, false positivity may result from overstaining, and this technique is not specific for amyloid. Thus, amyloid must be confirmed by apple green polarization, immunofluorescence, IHC, and/or electron microscopy. An alternative option to demonstrate amyloid deposits in cases with no paraffin embedded tissue available is to perform Congo red stain on frozen tissue (Figure 10). This technique is more sensitive than a Congo red stain performed on paraffin embedded tissue from our experience. Of note, positive controls should then, of course, also be performed on frozen tissues.
Thioflavin T is an additional sensitive but nonspecific fluorescent stain for amyloid, which is activated by blue light to emit yellow green fluorescence staining upon binding to amyloid . This test is more sensitive than Congo red in detecting a small amount of amyloid deposits. However, due to lack of specificity, it must be confirmed by Congo red apple green birefringence, IF, IHC, and/or EM.
AL amyloid nephropathy may coexist with other manifestations of the monoclonal protein, such as light-chain cast nephropathy, light-chain proximal tubulopathy, and rarely monoclonal immunoglobulin deposition disease. Any amyloid type may have coexisting other conditions in the kidney biopsy, such as acute tubular necrosis, diabetic nephropathy, thin basement membrane lesion, or arterionephrosclerosis.
6.2. Immunofluorescence microscopy
Immunofluorescence (IF) microscopy or immunohistochemistry is crucial for confirming the presence and for typing of amyloid nephropathy. IF is useful for detection of amyloid derived from Ig light and heavy chains. Amyloid deposits have a distinctive smudgy appearance of staining (Figure 11a). Restriction for light chain, either kappa or more commonly lambda, or for heavy-chain determents (γ or μ) must be demonstrated, in association with Congo red positivity, for a diagnosis of AIg amyloidosis. Therefore, IF staining for kappa and lambda should be routinely performed on all native renal biopsies. The findings of strong staining for a monoclonal Ig light chain with negativity for Ig heavy chains is diagnostic of AL nephropathy (Figure 11a and b). About 75% of AL nephropathy cases are due to monoclonal lambda deposits. The diagnosis of AH nephropathy is based on the presence of strong staining for a single Ig heavy chain with negativity for kappa and lambda light chains (Figure 12). AHL nephropathy shows intense staining for Ig heavy chain and a single Ig light chain (Figure 13a and b).
In addition to specific staining for proteins that comprise the amyloid, amyloid deposits often have low levels of nonspecific trapping with several reagent antibodies, including Ig and complements (Figure 14a and b). This varies, with different reagent antibodies and different specimens, and is more common with AA nephropathy than AL nephropathy. The basis for this low level of staining is not well understood, but may result from charge interaction between the amyloid and the reagent antibodies, contamination with serum proteins, and/or humoral reaction directed against amyloid fibrils. These low levels of nonspecific trapping sometime render the distinction between AA nephropathy and AL/AH/AHL nephropathy difficult. About 21% of AA nephropathy cases from a study by Nasr et al.  could not be diagnosed with certainty by IF and needed confirmation of amyloid type by mass spectrometry.
6.3. Electron microscopy
Transmission electron microscopy (TEM) is helpful in confirming the diagnosis of amyloidosis, but it is not helpful in determining the type of amyloid. At low magnification, amyloid deposits have a characteristic cottony appearance (Figure 15) that should alert the pathologist to investigate at higher magnification the possibility of amyloidosis. At high magnification, amyloid is composed of randomly arranged, elongated fibrils that measure 8–12 nm in diameter (Figure 16). Amyloid fibrils are associated with smaller, round structures, namely, amyloid p component. The fibrils are extracellular and located near mesangial cells in glomeruli and myocytes in the media of vessel walls in amyloid nephropathy. The amyloid fibrils may extend into the capillary walls and thus, foot process effacement is commonly seen in the segments of glomerular basement membranes overlying amyloid deposits. The podocyte cytoplasm adjacent to the amyloid deposits often shows condensation of actin cytoskeleton. When amyloid deposits extend into the subepithelial zone, the fibrils usually show parallel alignment (Figure 17). This is the basis for the JMS-positive feathery spikes that may be seen by light microscopy (LM).
6.4. Differential diagnosis
The differential diagnosis and distinction from other glomerular diseases are summarized in Table 2. By LM, the differential diagnosis includes any disease process that induces accumulation of acellular eosinophilic material in glomeruli, blood vessels, and interstitium. Accumulations of collagenous matrix, as in Kimmelstiel-Wilson nodules in diabetic nephropathy or sclerosis secondary to chronic immune complex glomerulonephritis or hypertensive nephrosclerosis, usually can be readily distinguished from amyloid by routine staining. As mentioned earlier, amyloid stains weakly with PAS and very little or negative with JMS, whereas sclerotic matrix is strongly PAS and JMS positive. Extensive glomerular deposits present in immune complex glomerulonephritis, fibrillary glomerulonephritis, immunotactoid glomerulopathy, and collagenofibrotic glomerulopathy may mimic amyloidosis on H&E stained sections; however, special stains, IHC, and EM demonstrate the distinctive features of each of these diseases. The Congo red stain is then necessary to confirm the diagnosis of amyloid nephropathy.
Light-chain deposition disease (LCDD) shares monoclonal immunoglobulin light-chain staining with AL nephropathy, but the pattern of staining is much different. LCDD typically has a more diffuse and regular distribution of staining that appears linear or ribbon-like along glomerular and tubular basement membranes. The expanded mesangium also shows globular staining in LCDD, in contrast to AL nephropathy, which typically shows a smudgy pattern of lambda or kappa light-chain staining with fuzzy border in the mesangium or along glomerular basement membranes, but no ribbon-like tubular basement membrane deposits.
|Differential diagnosis||Congo red stain||LM||IF||EM|
|Negative||Deposition of PAS positive |
and argyrophilic material in mesangium with occasional nodular formation
|Diffuse intense staining|
of single light chain
(more often kappa) along tubular and/or
glomerular basement membranes (ribbon-like), involving mesangium
(globular), and blood vessels
|Finely granular (punctate) or amorphous electron dense deposits along the inner aspect of glomerular basement membranes and outer aspect of tubular basement membranes|
|Light- and heavy-chain deposition disease||Negative||Deposition of PAS positive |
and argyrophilic material in mesangium with occasional nodular formation,
more mesangial hypercellularity
|Diffuse intense staining|
of single Ig heavy chain (more often IgG) and a single light chain along tubular and/or
glomerular basement membranes (ribbon-like), involving mesangium (globular), and blood vessels
|Finely granular (punctate) or amorphous electron dense deposits along the inner aspect of glomerular basement membranes and outer aspect of tubular basement membranes, occasional immune complex-type deposits, or rarely no electron deposits detected|
|Negative||Deposition of PAS positive and argyrophilic material in mesangium with occasional nodular formation,|
more mesangial hypercellularity
|Diffuse intense staining|
of single Ig heavy chain (more IgG3) along
glomerular basement membranes (ribbon-like), involving mesangium (globular), and blood vessels, no kappa or lambda staining
|Finely granular (punctate) or amorphous electron dense deposits along the inner aspect of glomerular basement membranes and outer aspect of tubular basement membranes, occasional immune complex-type deposits, or rarely no electron deposits detected|
|Fibrillary GN||Negative||Deposition of PAS|
positive and nonargyrophilic in mesangium and occasionally along glomerular basement membranes
|Smudgy staining for IgG (more often IgG4), C3, kappa, and lambda in mesangium and along capillary loops, about|
10% show restriction of
|Randomly arranged nonbranching fibrils size of 12-27 nm in diameter within mesangium, along outer aspect of glomerular basement membranes, and rarely along tubular basement membranes|
|Immunotactoid glomerulopathy||Negative||Deposition of PAS positive and nonargyrophilic in mesangium and occasionally along glomerular basement membranes||Smudgy staining for IgG (more often IgG1), C3, with light chain|
restriction (more kappa), staining in mesangium and capillary loops
|Microtubular or cylindrical structure with hollow cores with a size from 20 to 90 nm in diameter, arranged in parallel arrays, predominantly present in mesangium and subepithelial zone|
|Diabetic nephropathy||Negative||Accumulation of PAS positive and argyrophilic glycosylate products, Kimmelstiel-Wilson nodules, prominent glomerular basement membranes||Linear accentuation of|
IgG and albumin along glomerular and tubular basement membranes
|Diabetic fibrillosis with branching fibrils with a size of 10–25 nm in diameter in mesangium, thickened glomerular basement membranes|
|Collagenofibrotic glomerulopathy||Negative||Increase in mesangial matrix, argyrophilic, PAS positive material with intense blue|
staining on Masson trichrome stain
|Negative staining||curved and frayed, sometimes worm-like of comma-shaped fibers with transverse band structure with periodicity of 43–65 nm when sectioned transversely|
|Fibronectin glomerulopathy||Negative||Mesangial matrix accumulation of nonargyrophilic material with bright red staining|
on Masson trichrome
|May have nonspecific staining for IgG, IgM,|
|Granular to fibrillary substructures with a size of 14–16 nm in diameter|
By EM, the differential diagnosis includes other renal diseases that have deposits containing organized fibrillary or microtubular substructures, including fibrillary glomerulonephritis, immunotactoid glomerulopathy, and collagenofibrotic glomerulopathy. Fibrillary glomerulonephritis is characterized by glomerular deposits composed of randomly arranged, nonbranching fibrils that usually are 12–27 nm in diameter (Figure 18). The diagnosis of amyloidosis is unlikely if fibrils are larger than 20 nm. Immunotactoid glomerulopathy has organized microtubular substructures with hollow cores, measuring 20–90 nm (Figure 19). Collagenofibrotic glomerulopathy shows collagen fibrils deposited predominantly in the mesangium but sometimes can extend to subendothelial zone. The collagen fibrils appear curved and often frayed with periodicity of 43–65 nm. In diabetic fibrillosis, the fibrils are 10–25 nm, negative for Congo red and Thioflavin T. These fibrils tend to be shorter and more often aligned in parallel, slightly curved, and sometimes are oriented at right angles to mesangial cell surfaces, and may touch plasma membranes (Figure 20). Of note, the presence of diabetic fibrillosis in diabetic nephropathy does not appear to have any specific clinical connotations because a patient with this disorder behaves similarly clinically to those without fibrils . For each of the above conditions with substructure of material by EM, IF and light microscopic appearances, and negative Congo red stain, allow distinction from amyloidosis.
6.5. Typing of amyloid does matter
Amyloid typing is absolutely crucial for clinical management in order to avoid misdiagnosis and inappropriate, potentially harmful treatment, to assess prognosis and to offer genetic counseling if relevant. The classification is based on the nature of amyloid precursor plasma proteins. The initial step is IF, which is an important technique for AL typing. In AL nephropathy, there is restriction for either kappa or lambda light chain. In AH nephropathy, the deposits stain only a single subclass of Ig heavy chain, whereas a single heavy-chain and a single light-chain stain positive in AHL nephropathy. In cases where no frozen tissue is available, IF can be performed on paraffin embedded tissue by a pronase-digested technique. The paraffin-embedded tissue pronase-digested technique has less sensitivity than frozen tissue IF. Thus, negative IF staining for Ig light chains or heavy chain does not completely rule out AL nephropathy, AH nephropathy, or AHL nephropathy, as some monoclonal proteins may be mutated and not recognized by commercial antibodies. However, a negative IF study does typically suggest another type of amyloid nephropathy and requires further exploration by other modalities to diagnose the type of amyloid.
Current diagnostic methods, such as IHC technique using antibody-based amyloid typing, have limited ability to detect the full spectrum of amyloid forming proteins. Although IHC can be performed using commercially available antibodies against amyloid of the classes AL, AH, AA, AFib, ATTR, AApo AI, and Aβ2M , of these antibodies, serum amyloid A (SAA) IHC on paraffin-embedded tissue is the most extensively used and is considered the gold standard technique for diagnosing AA (Figure 21). AA IHC reveals a pattern of distribution matching that seen by LM. From our study, IHC on paraffin-embedded tissue for LECT2 is sensitive; however, it is not entirely specific for ALECT2 . It is recommended that the diagnosis of ALECT2 nephropathy should be confirmed by mass spectrometry analysis of renal tissues when the staining pattern shows equivocal Intensity .
In spite of the availability of IF and IHC, there are multiple drawbacks of these methods, such as sensitivity and specificity of commercial antibodies that are designed against only nonmutated proteins. Mutant proteins and proteins with conformational changes might be less reactive to commercial antibodies . For example, in 7–35% of the AL nephropathy cases, the amyloid deposits were negative for both kappa and lambda IF staining on frozen tissue . Therefore, be aware that a negative staining for light- and/or heavy-chain IF does not exclude AIg nephropathy. Of note, rare cases of amyloid nephropathy show more than one type of amyloid protein, leading to difficulty in typing. The drawbacks of these techniques may be solved by mass spectrometry, which is discussed below.
The direct technique of amyloid demonstration is based on proteomic analysis using laser microdissection/mass spectrometry (LMD/MS), which has the capability for identification of the many different proteins . This technique has a high sensitivity and specificity and solves many of the problems presented by other techniques .
LMD/MS has proved to be useful to determine the nature and type of the amyloid precursor protein in cases that could not be typed by routine IHC panels [45, 46]. The major advantage of LMD/MS over conventional IHC techniques in typing of amyloid is that LMD/MS is a single test that can identify and type the amyloid protein, in contrast to IHC that may require several antibodies staining multiple sections . Furthermore, LMD/MS is performed from paraffin-embedded tissue and requires no special treatment. The common indications for LMD/MS in amyloid nephropathy include amyloid type confirmation, insufficient tissue sample for IF or IHC studies but with remaining tissue in paraffin block, difficult cases on routine renal biopsy studies such as heavy-chain amyloidosis and familial and hereditary forms of amyloidosis [17, 48, 49]. The diagnosis of amyloidosis at the proteomic level using LMD/MS is purely based on the presence of large spectra of proteins, which have amyloidogenic properties, in addition to apolipoprotein E (Apo E) and SAP that are commonly present in all types of amyloid . Therefore, in AA nephropathy, large spectra numbers of serum amyloid-associated protein along with Apo E and SAP are present. In contrast, in ALECT2 and AGel nephropathy, large spectra numbers of LECT2 and gelsolin are present along with Apo E and SAP.
LMD/MS has been very helpful in achieving amyloid typing from formalin-fixed paraffin-embedded tissue. LMD/MS has also been critical for the typing of cases with limited antibody reactivity and in the discovery of new protein types of amyloid. From a study by Said et al., the type of amyloid in 16% of amyloid nephropathy cases could not have been typed without LMD/MS . In spite of these major advantages, LMD/MS also has a few drawbacks. As mentioned above, identification of amyloid proteins is purely based on the presence of large spectra for proteins, which have amyloidogenic properties within the analyzed sample. In a case of focal amyloidosis, a small amount of amyloid deposit may be obscured by Apo E, SAP, and various serum proteins. Furthermore, the observed peptide fragmentation data must be matched to known protein sequences that are available in the public data base, and thus, unknown protein sequences due to certain germ line polymorphisms or somatic mutations, may not be identified. Despite these drawbacks, the number of cases of amyloid with undetermined type has markedly decreased with use of this technique to 7%, with 3% of the sample insufficient for analysis [7, 8, 50]
6.7. Treatment and prognosis
The goal of current treatment approaches for AIg nephropathy is to eradicate the clone of plasma cells that produce amyloidogenic monoclonal light chains, Ig heavy chain, and Ig heavy and light chain. Patients with AIg nephropathy are usually treated with chemotherapeutic regimens appropriate for B-cell or plasma cell neoplasm. Melphalan-dexamethasone-bortezomib is commonly used as frontline regimen for patients with Stages I and II cardiac involvement . Patients with Stage III cardiac involvement or advanced chronic kidney disease (CKD) patients are generally treated with cyclophosphamide-bortezomib-dexamethasone [51, 52], which showed overall 81.4% hematologic response . High-dose intravenous melphalan followed by autologous stem cell transplantation (HDM/ASCT) to support bone marrow recovery has emerged as the most likely to eradicate the clonal plasma cells . Experiences from several treatment centers has suggested that 25–50% of patients who undergo such treatment have complete hematologic response, indicating that there is no evidence of ongoing production of monoclonal light chains, Ig heavy chain, or Ig heavy chain and light chain [52–54]. HDM/ASCT is generally offered to patients with Stages I or II cardiac involvement patients who have glomerular filtration rate (GFR) ≥ 30 mL/min in the absence of advanced other organ involvement [54–56].
Treatment of the underlying chronic inflammatory diseases, such as immunosuppressive agents for rheumatoid arthritis and inflammatory bowel diseases is beneficial in patients with AA nephropathy. The basis of modern treatment in AA nephropathy is still reduction of SAA production. Additionally, steroids and cytotoxic drugs, treatment with monoclonal antibodies against cytokines, particularly tumor necrotic factors (TNF) and interleukin-6 (IL-6), are effective in many cases . This approach of treatment is targeted not only at amyloid fibrils themselves but also at messengers in the acute-phase response. Other therapies, such as antisense oligonucleotides, have been suggested to specifically lower the expression of SAA in the liver . AA nephropathy caused by familial Mediterranean fever responds to colchicine . In familial amyloidosis, including AFib, ATTR, and AApo AI, in which the liver is the source of precursor protein, patients are treated with liver transplantation . A novel drug, R-1-[6-[R-2carboxy-pyrrolidin-1-yl]-6-oxo-hexanoyl]pyrrolidine-2-carboxylic acid is a competitive inhibitor of SAP binding to amyloid fibrils [59, 60]. This palindromic compound also cross-links and dimerizes SAP molecules, leading to their very rapid clearance by the liver, and hence produces a marked reduction in human SAP in the circulation . This mechanism of drug action potently removes SAP from the deposits of amyloid in human tissue and may provide a new therapeutic approach to AA amyloidosis and diseases associated with local amyloid deposition, including Alzheimer’s disease .
The prognosis for patients with AL nephropathy is generally poor and depends on systemic organ involvement, but survival can be prolonged with treatment [62, 63]. Patients with AL nephropathy have a median overall survival of 1–2 years [62, 63]. Patients with AA nephropathy have a better prognosis than those with AL nephropathy with the median survival varies between 2 and 10 years [13, 64]. In AL nephropathy and AA nephropathy, cardiac involvement is an independent negative predictive factor of patient survival . Patients with AA, AH, AHL, AFib, and ALECT2 nephropathy have longer overall survival compared with AL nephropathy, largely because of a lower rate of cardiac involvement [13, 65, 66]. The mean survival for AFib is 15 years , and the median survival for ALECT nephropathy is 62 months .
In AL nephropathy, kidney transplantation is ideally performed after production of amyloidogenic light-chain proteins has been eradicated. Kidney transplantation for systemic AL patients has a relative good outcome with 1- and 5-year patient survival of 75% and 67% and median graft survival of 5.8 years [67–69]. However, amyloidosis may recur in kidney transplants, depending on the amyloid type and progression of the underlying disease. In a large series from the UK, among 246 patients with AL nephropathy with renal failure, only 10% received kidney transplants , and of these, amyloidosis recurred in 28%; however, no graft was lost due to recurrent AL amyloidosis . Patient survival was best among patients who had achieved partial remission before kidney transplantation (8.9 years). In a French series of 59 recipients with AA amyloidosis, recurrence was documented in 14% at a median of 10 years posttransplant and was often associated with nephrotic range proteinuria . Among 10 recipients with hereditary AFib amyloidosis who received kidney transplantation only, recurrent AFib amyloidosis was detected in 70% and median graft survival was 7.3 years . In contrast, no recurrence was detected in the nine patients who received combined kidney and liver transplantation, but the mean renal graft survival was 6.4 years . Hereditary AApo I amyloidosis has recurred in 30% who received kidney transplantation only, and of these, one graft was lost to recurrent AApo I amyloidosis . There is no effective therapy for ALECT2 nephropathy . Because the precursor protein in ALECT2 is nonmutant, liver transplantation is likely ineffective . Kidney transplantation has been suggested as a treatment option for ALECT2 nephropathy patients with advanced renal failure . Although the disease may recur in about 20% of allografts, no graft was lost to recurrent ALECT2 nephropathy . Possible future therapies for ALECT2 nephropathy include reducing the supply of LECT2 (e.g., inhibiting the Wnt/β-catenin signal pathway), inhibiting amyloid fibril formation by blocking the binding of glycoaminoglycans to amyloid fibrils, promoting clearance of amyloid by immunotherapy, and promoting amyloid regression by SAP-targeted therapy.
The author thanks Dr. Agnes Fogo and Dr. Mark Lusco for their helpful advice.