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Atypical hemolytic uremic syndrome (aHUS) is a heterogeneous disease that is caused by defective complement regulation in over 50% of cases. Mutations have been identified in genes encoding both complement regulators [complement factor H (CFH), complement factor I (CFI), complement factor H-related proteins (CFHR), and membrane cofactor protein (MCP)], as well as complement activators [complement factor B (CFB) and C3]. More recently, mutations have also been identified in thrombomodulin (THBD), an anticoagulant glycoprotein that plays a role in the inactivation of C3a and C5a. Inhibitory autoantibodies to CFH account for an additional 5–10% of cases and can occur in isolation or in association with mutations in CFH, CFI, CFHR 1, 3, 4, and MCP. Plasma therapies are considered the mainstay of therapy in aHUS secondary to defective complement regulation and may be administered as plasma infusions or plasma exchange. However, in certain cases, despite initiation of plasma therapy, renal function continues to deteriorate with progression to end-stage renal disease and renal transplantation. Recently, eculizumab, a humanized monoclonal antibody against C5, has been described as an effective therapeutic strategy in the management of refractory aHUS that has failed to respond to plasma therapy. Clinical trials are now underway to further evaluate the efficacy of eculizumab in the management of both plasma-sensitive and plasma-resistant aHUS.
The online version of this article (doi:10.1007/s00467-010-1556-4) contains supplementary material, which is available to authorized users.
As the most common cause of acute renal failure in childhood, hemolytic uremic syndrome (HUS) is a clinical entity that arises as a result of a systemic thrombotic microangiopathy (TMA). Characterized by the triad of a microangiopathic hemolytic anemia, thrombocytopenia, and acute renal failure, over 90% of childhood HUS results from infection with Shiga-toxin producing Escherichia coli (STEC) and ‘typically’ presents with a diarrheal prodrome [1, 2]. Accounting for the remaining 10% of childhood HUS, atypical HUS (aHUS) is a heterogeneous disease that is associated with defective regulation of the alternative complement pathway in over 50% of cases (Table 1) [1, 3–6]. Mutations have been identified in genes encoding both complement regulators [complement factor H (CFH) [7–13], complement factor I (CFI) [14–24], complement factor H-related proteins (CFHR 1/3 and CFHR 1/4A) [1, 25, 26] and membrane cofactor protein (MCP) [27–31] in addition to complement activators [complement factor B (CFB) [18, 32, 33] and C3 [34, 35]. An additional 6–10% of aHUS cases are associated with inhibitory CFH autoantibodies that block the C-terminal recognition domain of CFH and reduce CFH binding to C3 [25, 36]. The majority of patients with CFH autoantibodies are also deficient for CFHR1, which shares structural and functional similarities to CFH and inhibits C5 convertase activity and thereby terminal complex formation [26, 37]. More recently, CFH autoantibodies have also been associated with mutations in other complement regulators such as CFH, CFI, and CD46 (MCP) . Furthermore, mutations in thrombomodulin (THBD), an anticoagulant glycoprotein which regulates C3b inactivation by factor I were recently identified in a further 6–10% of aHUS cases, thereby confirming previous associations between the coagulation cascade and complement regulation [39, 40]. A remaining 40% of aHUS cases are currently unaccounted for, and thereby necessitate investigation of additional susceptibility factors and demand further explanation of phenotypic presentation in pedigrees demonstrating incomplete penetrance. For a more detailed overview of the genetic etiology of aHUS, the reader is referred to several excellent reviews on this topic [5, 41–43].
In contrast to Stx-HUS, aHUS is associated with a poor long-term prognosis (Table 2), may be familial , and is characterized by frequent relapses  and progression to end-stage renal disease (ESRD) in at least 50% of cases . Disease recurrence following isolated renal transplantation is high and has been reported to occur in up to 30–100% of aHUS patients depending on the underlying complement defect [27, 46, 47]. Increasingly, it is recognized that a combination of mutations in genes encoding complement components, single-nucleotide polymorphisms (SNPs) and risk haplotypes must be present for aHUS to manifest in an individual [38, 48, 49]. Consequently, determination of the optimum therapeutic strategy can be challenging. The aim of this review is to provide an overview of the published experience of plasma therapy in aHUS associated with defective complement regulation. A second aim of this review is to highlight emerging evidence for a role for new agents that target the terminal complement cascade and may be the treatment of choice in cases associated with multiple complement defects.
Complement activation is a central component of the innate immune system, playing an important role in target opsonization, leucocyte recruitment, and cell lysis [50–53]. Complement can be activated by three major pathways: the alternative pathway (AP) is spontaneously and continuously active, the classical pathway (CP) is activated when antibodies bind their cognate antigen or the lectin pathway (LP), which is activated by the binding of mannose-binding lectin (MBL) to mannose residues on the surface of microorganisms. Complement activation occurs sequentially, beginning with initiation of activation, followed by C3 convertase activation and amplification, C5 convertase activation, which leads to assembly of the lytic membrane attack complex (MAC). The critical initiating step in complement activation is the cleavage of C3 to generate C3b and the formation of C3-convertase, which are protease complexes (AP, C3bBb; CP/LP, C2AC4b) (Fig. 1). Further amplification of activated C3b occurs when AP C3bBb is generated by convertase-generated C3b. Binding of C3b to the C3-convertase generates the C5-convertase with the capacity to bind and cleave C5, initiating formation of the MAC.
Under normal circumstances, circulatory C3 activation is low and is a tightly regulated process under the control of four major classes of regulatory proteins: fluid phase complement regulators, membrane-bound complement regulators, complement receptors, and surface-bound complement regulators  (Fig. 1). Regulation occurs at multiple steps including the inactivation of C3b or C4b, the dissociation of the C3/C5 convertase, or the inhibition MAC formation. Fluid-phase regulators circulate in plasma and include the alternative pathway regulators, complement factor H (CFH), and factor H-like protein (FHL), glycoproteins that are synthesized in the liver. FHL-1 is an alternative splice product of CFH . CFH regulates complement activation by at least three different mechanisms (Fig. 1). Firstly, CFH binds to CFI, a serine protease that mediates the proteolytic cleavage of the α-chain of C3b resulting in the formation of iC3b (co-factor activity) . Following further cleavage by CFI, iC3b forms the C3dg and C3c fragments using the membrane-bound complement receptor 1 (CR1 or CD35) [55, 56]. A second function of CFH includes the inhibition of the interaction between C3b and CFB and thereby blocks the formation of the C3bBb convertase complex (decay-accelerating activity). Furthermore, CFH promotes the dissociation of C3 convertase once they have formed (decay-accelerating activity). Binding of CFH by its C-terminus to sialic acid, glycosaminoglycans, or sulfated polysaccharides (heparin) increases the affinity of CFH for surface-bound C3b. Additional regulation is further achieved by the presence of five structurally related proteins to CFH (CFHR1-5) and are all composed of short consensus repeats (SCRs) that share different degrees of identity with SCRs in CFH . A regulatory function for CFHR1-5 proteins is suggested by their ability to bind C3b. Recent work has shown that CFHR1 blocks C5 convertase activity and interferes with C5b surface deposition and MAC formation [26, 58]. Similar to CFH, CFHR proteins are also synthesized in the liver but are present in much lower concentrations compared to CFH. In addition to regulation within the fluid phase, regulation also occurs at the level of the cell membrane. Several membrane-bound proteins have been shown to regulate complement and include complement receptors 1 and 2, complement decay accelerating factor (DAF), membrane-bound cofactor protein (MCP; CD46), protectin (CD59), and complement receptor of the immunoglobulin superfamily (CRIg) (Fig. 1). Membrane-bound factors control the three major complement activation pathways and inactivate both C3 and C4. Fluid-phase regulators, on the other hand, are more specific and regulate either the alternative, classical, or the lectin pathways and act almost exclusively on either C3 or C4.
Management of an aHUS crisis first begins with recognition and diagnosis. Clinically, HUS presents with a triad of microangiopathic hemolytic anemia (fragmented erythrocytes with low haptoglobin levels), thrombocytopenia, and acute renal failure. As set out in detail in the report published in 2006 by the European Study Group for HUS, the classification of HUS, thrombotic thrombocytopenic purpura (TTP) and related disorders is summarized in Table 1. An aHUS crisis occurring secondary to defective complement regulation should be considered if the following features are present: presentation before 6 months of age, insidious onset, previous episode of HUS, previous unexplained anemia, asynchronous family history of HUS or HUS post-transplantation of any organ, as recently described in the ‘Guidelines for the Investigation and Initial Therapy of Diarrhoea-Negative Hemolytic Uremic Syndrome’ published by the European Study Group for HUS . Investigation for enterohemorrhagic Escherichia coli should still be undertaken in the context of atypical features, as unusual presentations have been known to occur .
If a patient is suspected of having aHUS, then measurement of plasma complement C3, C4, CFH, CFH autoantibodies, CFI and CFB levels, and surface expression of MCP (CD46) on mononuclear leucocytes by FACS should be undertaken (Table 3). Furthermore, genetic mutation analysis for the susceptibility genes, CFH, CFI, CFHR1-5, CFB, CD46, and C3 should also be undertaken. If a patient has had a blood transfusion, then it is advisable to wait for 2 weeks before undertaking any mutational analysis. Details of the laboratories offering specialized investigation can be found on the following Web site: http://espn.cardiff.ac.uk.
It is important to note that while low levels of C3 may indicate complement dysregulation, there are occasions when C3 levels are normal . Activation of the alternative pathway may still be a feature and measurement of serum MAC and iC3b may prove to be a more useful indicator of alternative pathway activity with sMAC indicating the degree of activation of the terminal complement cascade and iC3b indicating the degree of inactivation of C3b. Elevated C3d levels are also an indicator of alternative pathway activation. Where C3 levels are normal, genetic investigation is still clearly warranted in such cases of aHUS [41, 60]. Furthermore, recent evidence has demonstrated that mutations in several complement genes can manifest in any one individual and therefore, mutation screening should be undertaken for all predisposing genes if possible. A summary of the known disease-causing mutations can be found on the following Web site: www.fh-hus.org and have been reviewed in detail elsewhere in this series. Careful consideration should also be given to other causes of aHUS, such as disorders of cobalamin metabolism as well as ADAMTS13 activity (a disintegrin and metalloprotease with thrombospondin motifs). While beyond the scope of this article, the reader is referred to other reviews on these disorders regarding diagnosis and management [61, 62].
Plasma therapy is considered the first-line therapy for aHUS [3, 6, 41, 63, 64]. While there have been no controlled clinical studies, the introduction of plasma therapy into the management of aHUS was associated with a decrease in mortality from 50 to 25% [65, 66]. Plasma-based therapies may be classified as plasma infusion (PI) or plasma exchange (PEX). Plasma infusion is thought to replace defective complement components and regulators with functional proteins [67, 68]. Plasma exchange offers the additional advantage of removal of mutant CFH, CFI, CFB, C3, and CFH autoantibodies while restoring functional complement regulators.
Given the emerging evidence for the existence of a combination of complement defects and risk haplotypes in disease manifestation, it is no longer sufficient to consider the management of aHUS as simply a matter of replacing a single deficient factor by PI or removal of a mutant factor by PEX. As a result, the European Working Group on HUS has recently published consensus guidelines with the aim of establishing a standardized approach to the initial management of aHUS and thereafter with a view to auditing this approach again in 3 years . As there have been no randomized controlled clinical trials investigating the efficacy of either PI or PEX in the management of aHUS, the published guidelines are expert consensus opinions based on combined personal experiences and published case reports.
Guidelines suggest that plasmapheresis should be commenced within 24 h of initial presentation along with supportive treatment (transfusion, dialysis, antihypertensive therapy). However, in clinical practice, this may not always be possible due to the time that it may take to rule out infection with for EHEC. Neurological symptoms in HUS can be a consequence of many factors such as cerebral microangiopathy with ischemia and infarction, hypertension, and cerebral edema arising from metabolic disturbances. The presence of these symptoms indicates a progressive disease process and following correction of hypertension and metabolic disturbances with dialysis, plasmapheresis should be instituted promptly in those cases suspected of having aHUS. Initially, 1.5 times the expected plasma volume should be exchanged or a plasma infusion of 20–30 ml/kg of body weight should be administered . Replacement with whole plasma fraction such as virus-inactivated pooled plasma or individual units of fresh frozen plasma (FFP) from screened donors is recommended . PEX may be achieved by plasma filtration or via a centrifugal separator, according to local practice and expertise. Daily PEX is recommended for the initial 5 days followed by five sessions per week for the next 2 weeks and then tapered to three sessions per week for the subsequent 2 weeks .
Following initiation of plasmapheresis, it is advisable to monitor the full blood count, electrolytes, and serum creatinine daily to determine whether the therapy has made any impact on the degree of hemolysis and renal dysfunction. Similarly, it may also be helpful, in those cases presenting with low C3 levels, to measure daily C3 levels throughout plasmapheresis to help determine the optimal therapeutic regime in individual cases for the management of subsequent disease flares. The current guidelines suggest that remission has been achieved if platelet counts are sustained >150×109/l for 2 weeks and there has been no hemolysis as determined by the presence of fragmented red cells, elevated lactate dehydrogenase, and low haptoglobins . Recurrence of thrombocytopenia and hemolysis after 2 weeks of recovery of both parameters signifies a relapse and reinstitution of plasmapheresis is recommended if previously successful. Furthermore, for auditing purposes, it is recommended that the renal function be graded as normal [glomerular filtration rate (GFR) ≥80 ml/min/1.73 m2 as determined by the Schwartz formula or by a formal clearance assay], renal impairment whereby plasma creatinine level is elevated for age or GFR <80 ml/min/1.73 m2 or renal failure (requiring dialysis). Furthermore, the presence of proteinuria and hypertension (expressed as a centile based on age and gender) including number of antihypertensive agents should be recorded.
Following a period of 3 years, the European Study Group on aHUS aims to audit the proportion of cases investigated and the resultant yield from the proposed investigations to determine what proportion were treated according to the guidelines and the proportion that were withdrawn or did not meet the criteria for treatment according to the guidelines. Importantly, the objective of the recommended guidelines also propose to determine the proportion of patients entering hematological remission based on the recommended therapy schedule for the first month and those that have preserved or loss of renal function by the end of the first month.
With the advent of extended mutational analysis in aHUS patients, it is now very clear that disease manifestation is more frequently associated with a combination of risk factors that not only includes mutations in key complement components and regulators but also risk haplotypes and SNPs in other complement components. In the ensuing text, we review the published experience of either PI or PEX in cases that have previously been reported as defects in a single component. Response to plasma therapy in relation to underlying genetic defects should be interpreted with caution as it is possible that further defects would be found in such patients if they were to undergo further genetic screening. Therefore, the objective of the ensuing text is to highlight the outcome of individual cases based on the reported therapeutic regimen employed and thereby demonstrate the divergent outcomes even amongst those cases that appeared to have similar underlying genetic defects.
Deficiency of CFH may be either quantitative or functional. A quantitative deficiency is defined as CFH plasma levels below half of normal . Complete deficiency is extremely rare and is defined by the total absence or severe reduction in CFH levels. To date, 34 CFH-deficient patients have been described from 16 families [9, 70–81]. Renal disease has been reported in 28 of these 33 cases, of whom 16 developed aHUS [67, 72, 76–79, 82–85]. The clinical presentation of those with complete CFH deficiency and their complement profile, plasma therapy regimen, and outcome are summarized in Supplementary Table 1. If plasma therapy such as PI with FFP is initiated early in the course of the disease when the serum creatinine level is normal or only slightly elevated, then it may be possible to preserve renal function for a number of months or years . However, as there may be more than one defect present, recommendations now advocate for PEX as the initial treatment regimen with the additional advantage of removal of mutant proteins while restoring functional proteins. Functional CFH deficiency is more common than complete CFH deficiency and is associated with a normal CFH level. While mutations have been found throughout the gene, over 80% occur within the region that encodes the C-terminal domain of the protein and results in reduced binding of C3b and to polyanions leading to impaired function of CFH. For patients, with a functional deficiency of CFH, the response to plasma exchange with FFP replacement has been shown to be effective [87–91] (Supplementary Table 2). As mutations of CFH are heterogeneous, a strategy of intensive and prophylactic PEX may not be necessary in all patients with CFH mutations and therapy should be tailored according to individual patient response. Furthermore, resistance to long-term plasma therapy has been reported in patients [88, 92]. Although the underlying mechanisms for the development of resistance require investigation, a plausible reason may be the development of autoantibodies to CFH or other complement proteins for which assays are not readily available.
As the strategy of prophylactic PEX is expensive, necessitates creation of an arteriovenous fistula, central venous access, and implies life-long regular treatment in a hospital, the development of a purified human plasma-derived CFH concentrate may provide sufficient CFH in a small volume to replace PEX and thereby reduce the risks associated with central venous access and volume overload. Whether it will suffice to administer it alone or in combination with PEX will have to be determined in the future. Development of such a concentrate is currently being undertaken by the Laboratoire Français du Fractionnement et des Biotechnologies (details can be found at the Web site: www.emea.europa.eu/pdfs/human/comp/opnion/52123506en.pdf).
Recent studies have suggested a pathogenic role for CFH autoantibodies in the development of aHUS [25, 93, 94]. Functional studies have demonstrated that CFH autoantibodies bind to the C-terminus of CFH and thereby inhibit C3b binding, leading to enhanced complement activation and red cell hemolysis . Furthermore, deficiency of the complement regulatory proteins, CFHR1 and CFHR1/3, has also been described in patients with CFH-autoantibody associated aHUS (Supplementary Table 3) [25, 38, 96–98].
Current recommendations propose that a trial of PEX therapy is warranted in an attempt to remove CFH autoantibodies [21, 99]. PEX provides an excess of CFH that may saturate and neutralize the autoantibody activity and partially restore functional CFH circulating levels, while removing the autoantibody from the circulation . In the pre-transplantation setting, intravenous immunoglobulin (IVIG) and rituximab (the anti-CD20  antibody) have been utilized with efficacy in preventing recurrence post-transplantation and is described in detail in the section entitled 'Transplantation in aHUS'.
Mutations in CFI account for around 10% of aHUS cases  and similarly to CFH, result in either a quantitative or functional deficiency of CFI protein . A poor prognosis exists for aHUS associated with CFI mutations with over 50% of reported cases progressing to ESRD following initial presentation. Approximately 40% of CFI mutations result in low levels of CFI . Therefore, replacement with plasma theoretically should restore deficient CFI in patients who have only CFI mutations. However, as outlined in Supplementary Table 4, the response to either PI alone or PEX is often inadequate and this may be due to the occurrence of concomitant complement defects or risk haplotypes that were not detected at the time of reporting.
Patients carrying CFB gain-of-function mutations develop aHUS as a result of decreased decay of the C3bBb convertase . Of four patients in whom details of treatment has been reported, plasma therapy was administered to three patients, with one patient receiving PEX only, one patient receiving PI only, and one patient receiving a combination of both. Disease progressed in all patients despite plasma therapy with four patients progressing to ESRD. The fourth patient, at the time of reporting, had moderate renal insufficiency but had not received plasma therapy. An additional patient who also carries a CFI mutation experienced immediate disease recurrence in the renal allograft following transplantation and despite treatment with intravenous immunoglobulin (IVIG), ESRD has progressed in the allograft almost 5 years later . Patients carrying gain-of-function CFB mutations are likely to require very large amounts of FFP and very frequent PEX in order to overcome the overproduction and resistance to decay of the alternative pathway C3 convertase to C3bBb. This will need to be confirmed by serial measurements of complement during therapy in future studies.
Patients carrying MCP (CD46) mutations tend to recover completely from aHUS relapses [24, 46, 47]. None of the children reported so far develop ESRD at 1 year from initial presentation while 86% remain dialysis-free in the long term [24, 46, 47]. Evidence from individual case reports  in addition to the reports from the Italian  and French series  suggest that plasma therapy is unlikely to be of therapeutic benefit in CD46 mutation-associated aHUS. In the French series, favorable outcome occurred in eight (89%) of nine episodes that were treated with plasma therapy and 15 (88%) of 17 untreated episodes . Caprioli et al. reported in the Italian series that complete or partial remission (defined by recovery of hematological parameters with persistence of renal dysfunction) was achieved in 91% of plasma-treated episodes but also in 100% of the non-treated episodes . However, in those patients who did not recover spontaneously, it was not possible to conclude that plasma therapy failed because it was not adequately administered. Furthermore, a recently reported fifth case by Davin et al. was initially treated with daily PEX and recovered normal renal function . However, recurrence of aHUS over the subsequent 4 years was associated with a progressive decline towards ESRD despite continuous prophylactic PEX. The lack of a response in aHUS patients carrying MCP mutations is likely owing to the fact that MCP is a membrane-bound protein and its role is limited to endothelial cells, and as a result, is not associated with systemic complement dysregulation.
Recurrence post-transplantation has been reported in three retrospective cohorts of aHUS patients with defective complement regulation [24, 46, 101]. Within the larger cohorts, mutations in CFH, CFI, or MCP were reported in around 50% of aHUS patients and post-transplant recurrence was reported in 33% , 37% , and 60%  of grafts.
Transplantation in patients carrying CFH mutations is particularly unfavorable with an almost 80–100% recurrence rate reported, depending on the degree of quantitative deficiency of CFH and the concurrence of other complement defects. In one series, 74% of CFH mutated patients had HUS recurrence from 2 days to 22 months after transplantation; 93% (13/14) of recurrences induced graft loss, most often (85.7% of recurrences) within the year after recurrence. Only one of the 15 grafts with recurrence was functioning at 6 years of follow-up . Similarly poor outcomes have been reported by the UK (78%) , and Italian Registries (83%) . For those with CFI mutations, a similar rate of recurrence has been reported with 11 of 12 grafts failing in eight recipients due to disease recurrence [15, 20, 36, 47, 102]. While recurrence data for CFB and C3 mutations are also emerging [90, 103], conclusions regarding appropriate therapeutic strategies cannot be made until more cases are reported.
Combined liver-kidney transplantation has recently been advocated for patients with CFH and CFI mutations as CFH and CFI are circulating factors synthesized by the liver [6, 47, 104–106]. Justification for liver transplantation comes from the fact that mutant CFH or CFI will continue to be produced by the liver in those who receive a renal transplant only and therefore, recipient mutant CFH or CFI may still not regulate complement activation sufficiently in the donor renal allograft, thereby leaving it susceptible to disease recurrence. Initial reports of orthotopic liver transplantation in aHUS were disappointing with the first CFH-deficient recipient experiencing acute hepatic failure during the liver transplant . A second liver was transplanted at day 26, resulting in aHUS remission, the patient later developed neurological sequelae from severe hepatic encephalopathy . A 2½-year-old was the second recipient who received a liver transplant from his father following severe, recurrent hemolytic/thrombocytopenic episodes but had preserved renal function. Following transplantation, the patient suffered fatal liver failure immediately following transplantation following a period of graft hypoperfusion that led to complement activation and microvascular thrombosis and infarction in the liver allograft. He died 10 months later from lymphoproliferative disease and recurrent infections associated with features of HUS . However, despite the poor outcome for both of these cases, normalization of CFH levels post-transplantation was demonstrated for the first patient and recurrence was avoided in the second, thereby suggesting that combined liver-kidney transplantation may be an effective strategy for preventing disease recurrence in patients with aHUS. Subsequently, a modified approach was employed whereby pre-transplantation PEX was administered to remove mutant CFH in addition to peri-transplantation PI after hepatectomy and before donor liver implantation, which led to increased bioavailability of CFH during acquisition of allograft liver function . Furthermore, low-dose enoxaparin and aspirin were employed to counteract the enhanced thrombogenicity of the allograft endothelium . Furthermore, a role for isolated liver transplantation may also be considered in patients who have frequent relapses but stable renal function. While a paucity of data exists, preliminary guidelines have been proposed based on experience drawn from about one dozen liver-kidney transplants for aHUS worldwide over the past decade. Successful liver-kidney transplants have been undertaken in four centers worldwide and should be undertaken in an experienced center given the high rate of postoperative complications. It is likely that plasma requirements will vary between individuals to control complement activation which can be exacerbated on reperfusion of the transplanted liver. The amount of required plasma may also depend on how long it takes for the transplanted liver to establish its synthetic function and the rate of synthesis of complement regulatory proteins. Patients with surgical complications leading to prolonged warm ischemia and delayed liver graft function will probably require more plasma over an extended period.
A paucity of literature exists as to the success of isolated renal transplantation of patients with CFH autoantibodies. Recently, Kwon and colleagues reported successful renal transplantation in a 10-year-old girl with CFH autoantibody-associated aHUS . Prior to transplantation, therapy consisted of prednisolone, azathioprine, and PEX in an attempt to decrease the CFH autoantibody titre. A decrease in CFH autoantibody titres following six sessions of PEX (50 ml/kg/session over 15 days) was observed. On cessation of PEX, CFH autoantibody titers rose again within a month, but on initiation of a second course of PEX, subsequently decreased again, thereby suggesting a potential beneficial role for PEX in removing CFH autoantibodies . No recurrence of disease occurred following an exchange program of 50 ml/kg/session with FFP substitution immediately prior to surgery and continued daily during the first week following transplantation with subsequent tapering over the following 4 months . HUS did not recur in the following 2 years post-transplantation. Further reports of successful renal transplantation in CFH-autoantibody-associated aHUS without recurrence have recently emerged and without adjuvant rituximab [38, 98]. Induction of immunosuppression with basiliximab, the IL2 receptor antagonist, in addition to high-dose corticosteroids and mycophenolate mofetil was utilized as a steroid-sparing agent and no disease recurrence, thereby suggesting that this immunosuppressive regimen may be efficacious in certain cases of CFH-autoantibody-associated aHUS.
Familial cases of aHUS associated with complement defects have been reported [30, 46, 109] and therefore, following presentation of the index case, it would be prudent to discuss the possibility of disease manifestation in other family members. In our opinion, urinalysis and blood pressure monitoring should be undertaken in all family members on at least an annual basis. If proteinuria or hypertension became evident, then further investigation of renal function, complement profile and genetic testing for complement defects may be warranted. In the event of transplantation, living-related organ donation is contraindicated in patients with CFH, CFI, CFB, and C3 mutations owing to a significant recurrence risk in the renal allograft [6, 47]. Owing to the incomplete penetrance of HUS associated with complement defects in family members, the genetic variability within family members in addition to a number of SNPs, living-related donation is not without risk. Furthermore, the remaining kidney in the donor may also be susceptible to disease manifestation where it has been previously reported that four donors developed HUS in their native kidneys following donation [47, 110]. If living-related donation is the only possible option, complete genotyping of all known complement abnormalities of the related donor should be performed. In the absence of a mutation or risk haplotype, the donor must be informed that there remains a possibility that he might have some unknown risk factor of developing HUS after kidney donation .
Emerging evidence has shown that patients presenting with aHUS can have a constellation of genetic defects that result in over-activation of the alternative complement cascade [66, 103]. Such patients represent a significant therapeutic challenge and, as a result, disease flares may be best treated with agents that target the membrane attack complex (MAC) composed of C5b-9, the final effector pathway of complement activation. Eculizumab, a humanized monoclonal antibody against C5, has recently been shown to be an effective treatment in aHUS [100, 103, 111–113]. Initially, eculizumab was employed in the therapy of patients with paroxysmal nocturnal hemoglobinuria where it was shown to markedly reduce intravascular hemolysis, the need for transfusion, and patient fatigue [114, 115]. It has also been shown to be effective in patients with rheumatoid arthritis, systemic lupus erythematosus, myocardial infarction, membranous nephritis, and those who have undergone coronary artery bypass surgery . Biochemically, eculizumab is an IgG immunoglobulin comprised of human constant regions and murine complementarity determining regions grafted onto human framework light- and heavy-chain variable regions. Eculizumab is composed of two 448-amino-acid heavy chains and two 214-amino-acid light chains and has a molecular weight of approximately 148 kDa. Eculizumab does not inhibit C5 activity in animal sera but does bind to human tissues, including smooth and striated muscle as well as renal proximal epithelium. In animal studies, eculizumab was found to cross the placental barrier and show fetal morbidity and mortality . Details can be found on the following Web site http://www.emea.europa.eu/humandocs/Humans/EPAR/soliris/soliris.htm.
Complement C5 is split by C5 convertase into C5a and C5b (Fig. 2a). C5a increases the permeability of blood vessels and attracts inflammatory cells by chemotaxis. C5b binds to other complement components (C6, C7, and C8). The C5b-8 complex is expanded with C9 to form the MAC. MAC binds and permeabilizes bacterial walls (e.g. Neisseria), thereby killing the microorganism. Eculizumab is a long-acting humanized monoclonal antibody targeted against complement C5 (Fig. 2b) . The plasma half-life is estimated to be about 11 days (personal communication with Alexion Pharmaceuticals). It inhibits the cleavage of C5 into C5a and C5b and hence inhibits deployment of the terminal complement system including the formation of MAC.
Five aHUS patients treated with eculizumab have been reported in the literature thus far [100, 103, 111–113]. Two patients have been treated in the pre-transplantation setting [111, 112] while the remaining three have received therapy post-transplantation [100, 103]. In addition to the aforementioned five cases reported in the literature, an additional 14 patients have been treated with eculizumab, ten of whom achieved stable remission . Of those reported and receiving treatment in the pre-transplantation setting, the first report was that of an 18-month-old male infant with congenital aHUS who had frequently relapsing aHUS . Following the development of resistance to plasma therapy, a fourth relapse at 18 months of age was treated with weekly eculizumab at 300 mg doses weekly for 3 weeks, which was then followed by 600 mg every 2 weeks thereafter. An improvement in the hematological and biochemical parameters was noted within 48 h of initiation of therapy and subsequently, plasma therapy was discontinued within the first week of eculizumab therapy. While a genetic defect in complement regulation was not identified in this infant and the hematological parameters improved just prior to the initiation of therapy, additional evidence for the beneficial effects of eculizumab in acute aHUS were recently reported in an adolescent with unclassified aHUS . PEX was initially effective in facilitating the temporary improvement of renal function. On tapering the plasma exchanges to three times per week, aHUS activity progressed to ESRD. After 12 weeks, eculizumab was initiated and was effective in terminating the microangiopathic hemolytic process in two aHUS relapses . However, after normalization of complement activity, aHUS recurred and ultimately led to anuric ESRD. A similarly beneficial experience has been reported in three renal transplant patients who experienced aHUS recurrence [100, 103, 113]. The first was a 30-year-old female with a combined CFH mutation (Y475S) and CFHR1 deletion . She was treated with 600 mg of eculizumab after her renal function deteriorated following failure of PEX initiated for recurrence of aHUS in a second allograft. She had lost her first allograft due to disease recurrence that was resistant to plasma 7 years earlier. Following commencement of eculizumab, the transplant function recovered with resolution of the total complement hemolytic activity and 8 months later, the patient’s renal graft function is stable at the time of reporting . Since this initial report, a further two cases have been reported. A 17-year-old girl with aHUS associated with a CFH mutation (S1191L) was plasma-dependent and successfully treated with eculizumab following the development of severe allergic reactions to plasma after her third allograft . The fifth reported case treated with eculizumab is that of a 42-year-old woman with a heterozygous gain-of-function mutation (R570Q) in the C3 gene . Following aHUS recurrence in her second renal allograft, she underwent intensive PEX to which she responded. However, PEX was discontinued as she experienced side-effects of diarrhea and fatigue. Treatment with eculizumab was initiated 4 days after the final session. She received four doses of eculizumab, 900 mg IV every week, followed by a maintenance dose of 1,200 mg every 2 weeks. After 7 months of eculizumab treatment, and without concomitant plasmapheresis, schistocytes decreased to 0.5%, haptoglobin increased to within normal limits, creatinine levels stabilized, and no further episodes of diarrhea were reported. The need for blood transfusions was significantly reduced and they were stopped 4 months after continued eculizumab treatment. Therefore, clearly there is a role in the event of recurrence of aHUS. Whether a role exists for prophylactic eculizumab in the prevention of recurrence and thereafter its safety will have to be determined in future studies. Duration of therapy should be determined by the maintenance of remission of hemolysis and thrombocytopenia. In the current trials involving adolescents and adults, eculizumab will be provided for 6 months. Enrollment has just been completed and the results of the study are anticipated later this year. It is likely that the required duration of therapy will vary from patient to patient depending on the underlying complement defects.
Eculizumab is administered as an intravenous infusion and pharmacodynamic assays demonstrate that inhibition of C5 sufficient to prevent hemolysis occurs at eculizumab plasma concentrations in excess of 35 µg/ml . Eculizumab (Soliris©, Alexion Pharmaceuticals) is administered as an infusion in adults at a dose of 600 mg over 25 to 45 min with therapeutic doses of the drug achieved within 1 h of infusion. The frequency of administration can be weekly and the dose further increased to 900 mg in adults in the fifth week. Thereafter, maintenance doses can be administered on an alternate weekly basis at 900 mg. Currently, there are no dosage recommendations for children under 12 years of age. However, with the advent of trials due to commence later this year, in younger children at acute presentation and in the pre-transplantation setting, guidelines for appropriate dosage for this age-group may be further developed.
The main side-effects of therapy are an increased susceptibility to meningococcal infection as a result of MAC inhibition. MAC plays a crucial role in eliminating neisserial infections and defects in components of MAC are strongly associated with recurrent bacterial infections involving encapsulated Gram-positive or Gram-negative organisms such as neisserial and pneumococcal infections. It is advisable that patients carry a special card stating the risks and symptoms of susceptible infections such as Neisseria meningitidis when they are receiving treatment with eculizumab. Patients should be vaccinated against Neisseria meningitidis at least 2 weeks before treatment with eculizumab and revaccination is also recommended according to current guidelines. While antibodies will be generated following immunization, they will be of reduced efficacy as partly their action will rely on the terminal complement pathway. As a result, prophylactic antibiotics should also be considered for the duration of the treatment.
Owing to the reported benefits of eculizumab in individual cases of aHUS, its efficacy is currently being evaluated in a number of controlled clinical trials (ClinicalTrials.gov numbers NCT00844545, NCT00844428, NCT008838513, NCT00844844). Of these, one trial is an open-label controlled trial of eculizumab in adolescent patients (aged 12–18 years) with plasma therapy-sensitive aHUS (NCT00844428). This study is currently in phase II with recruitment just recently completed. The treatment period is for 6 months with analysis of results expected by the end of this year. Eligibility criteria can be found on the Web site: http://clinicaltrials.gov/ct2/show/NCT00844428. A second trial is determining the efficacy in adolescent patients with plasma therapy-resistant aHUS (NCT00844844). Resistance to plasma therapy is defined as a decrease in platelet count despite at least four plasma therapy (PT) treatments in the first week immediately prior to screening (screening platelet count, 150×109/l and at least 25% lower than remission platelet count or if remission counts not available, screening platelet count <75×109/l). Details of related adult studies can be found on the following Web site: http://clinicaltrials.gov/ct2/show/NCT008838513 (adult patients with therapy-sensitive aHUS) and http://clinicaltrials.gov/ct2/show/NCT00844545 (adult patients with therapy-resistant aHUS). Primary outcome measures include the assessment of the efficacy of eculizumab in reducing TMA while secondary outcome measures include additional efficacy endpoints related to manifestations of TMA, pharmacokinetics and pharmacodynamics of eculizumab in patients with aHUS, overall safety, and tolerability of eculizumab. Inclusion and exclusion criteria are as outlined in Tables 4 and and5.5. It is hoped that further trials addressing the efficacy and determining appropriate dosage will be developed for patients less than 12 years of age in the near future both in the setting of acute presentation as well as the peri-transplantation period.
Atypical hemolytic uremic syndrome is a heterogeneous disease in which defective complement regulation currently accounts for around 50% of cases. Defects in more than one complement regulator are frequently present in many aHUS cases and thereby pose a significant therapeutic challenge. As a result, targeting the final effector pathway in complement activation may provide a more effective strategy in modifying disease progression. Recent reports propose an efficacious role for eculizumab in the management of aHUS. Results of the recently completed trial in adolescents are eagerly awaited. Enrollment of childhood cases of aHUS in a much anticipated trial is expected to commence later this year. Within the peri-transplantation setting, it will be important to determine the role of prophylactic eculizumab in the prevention of recurrence of aHUS.
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An erratum to this article can be found online at http://dx.doi.org/10.1007/s00467-012-2333-3.