FormalPara Key Points

Diagnosis of Fabry disease in males includes the detection of decreased α-galactosidase A activity and in females the determination of a disease-causing mutation.

Current treatment options of enzyme replacement therapy and chaperone therapy can improve disease burden and quality of life.

New therapy options include modified enzyme replacement therapy, substrate reduction therapy, and gene therapy.

1 Introduction

Fabry disease (FD) is an X-linked lysosomal storage disorder based on a deficiency in α-galactosidase A (GLA/AGAL) activity causing a progressive, life-threatening multisystemic disease due to intracellular accumulation of glycosphingolipids (mainly globotriaosylceramide [Gb3)] [1]. The aim of this article is to provide a brief overview of the clinical picture of patients with FD, the diagnostic confirmation, and interdisciplinary clinical management, with an additional special focus on current and future therapeutic options.

1.1 Overview of Epidemiology and Pathogenesis

FD affects men and women with an incidence of 1:40,000–1:117,000, although newborn screenings have pointed to higher incidences of 1:3100–1:1250 in males [2, 3]. Disease-causing mutations are detected in the GLA gene coding for AGAL, which is located on the long arm of the X chromosome (band q22), has a length of 12 Kb, and consists of 7 exons and 6 introns. Currently more than 1000 different GLA mutations are known, while most patients carry "private" (family-specific) mutations. Due to X-linked inheritance, family history is important and genetic counseling is recommended for every family with member who has FD.

Since almost all body cells accumulate Gb3, numerous organs/organ systems such as kidneys, heart, blood vessels, and the central and peripheral nervous system are affected, and patients show varying degrees of progressive functional deficits.

1.2 Clinical Picture and Diagnostics for Diagnosis Confirmation

FD patients suffer from a multisystemic disease with progressive (dialysis-dependent) renal insufficiency, cardiomyopathy with sometimes life-threatening cardiac arrhythmias, recurrent strokes, gastrointestinal pain, and neuropathic pain of the extremities, which can lead to Fabry crises (Table 1 and Fig. 1) [1, 4]. Due to the random inactivation of one of the two X chromosomes in each cell during early embryogenesis, the variability of the clinical picture is greater in women than in men [5].

Table 1 Classical manifestations in Fabry disease according to age
Full size table
Fig. 1
figure 1

Fabry disease is a multisystemic disease. TIA transient ischemic attack, WML white matter lesion

Full size image

FD can be suspected in the presence of a the family history and/or from the evidence of the typical manifestations. In males, the determination of AGAL activity in blood leukocytes or from dried blood spots is the method of choice for confirmation a diagnosis. A pathologically low AGAL activity indicates the presence of FD. In females, molecular genetic testing demonstrating a disease-causing mutation in the GLA gene is necessary to confirm the diagnosis, since women with FD often present with AGAL activities within the reference range. In men with pathologically decreased enzymatic AGAL activity, molecular genetic testing should be used to detect the underlying mutation in order to select an appropriate FD-specific therapy (see below). As a marker of disease burden, a pathologically elevated globotriaosylsphingosine (lyso-Gb3) in plasma or urine can contribute to improved diagnosis and subsequent monitoring. In unclear diagnostic cases (disputed mutation, ambiguous AGAL activity and lyso-Gb3 values, comorbidities) organ biopsies may be helpful. If biopsies are performed, electron microscopic multilamellar myelin bodies (so-called "zebra bodies" or "paper roll phenomenon") can be detected, which are pathognomonic for FD, but require special sample preparations. Prenatal diagnosis can be performed by measuring AGAL activity in chorionic villi or cultured amniotic cells and, in the case of a mutation known in the family, by molecular genetic methods (see Table 2).

Table 2 Concomitant medications and strategies in Fabry disease
Full size table

2 Therapy Goals and Treatment Recommendations

Once the diagnosis is confirmed, patients should be referred to an interdisciplinary Fabry center for initial examination, therapy planning, and therapy initiation. The following therapeutic goals should be aimed for in the context of multimodal care [6, 7]: (1) Reduction of complaints (especially pain reduction), (2) delaying/preventing the progression of organ manifestations (especially in the kidney, heart, and central nervous system), (3) improvement of quality of life, and (4) normalization of life expectancy.

Male FD patients generally have a higher risk of worse disease progression and outcome compared to females. Consequently, the international recommendations for initiating FD-specific treatment in adult male and female patients with classic or late-onset mutations reflect a personalized treatment approach that takes into account the natural history of the specific disease phenotype [6]. In an adult male with a classic Fabry mutation, FD-specific treatment should be considered regardless of the patient’s symptomatology (symptomatic or asymptomatic). Treatment decisions may be influenced by advanced patient age and severe comorbidity. In a female with a classic Fabry mutation, initiation of FD-specific treatment is warranted if she is symptomatic and symptoms/manifestations are indicative of organ involvement. In an asymptomatic woman with a classic Fabry mutation, initiation of FD-specific treatment should be considered if there is laboratory, histologic, or imaging evidence of renal, cardiac, or central nervous system damage. In males and females with a later-onset Fabry mutation (such as p.N215S), FD-specific treatment should be considered when there is laboratory, histologic, or imaging evidence of renal, cardiac, or central nervous system damage, even in the absence of typical Fabry symptoms. The abnormalities should be due to FD; this may require histologic evaluation or biochemical evidence of Gb3 accumulation. In the absence of detectable FD-related tissue pathology or clinical symptoms, FD-specific treatment may not be appropriate, especially in heterozygous female patients. These patients should be monitored regularly by a multidisciplinary care team. Patients with "benign," non-disease-causing GLA variants/polymorphisms should not be treated with any FD-specific therapy.

Therapeutic goals are not always achievable in clinical practice. Consensus recommendations [6, 7] provide guidance by establishing goals between clinicians and patients and considering treatment-related challenges to enable individualized treatment, optimize patient care, and improve quality of life. The patient-management algorithm addresses the need for early disease-specific therapy to delay or slow disease progression, as well as nonspecific adjunctive therapies that prevent or treat organ damage and stabilize quality of life [6].

3 Fabry Disease-Specific Current Treatment

Currently approved medications including enzyme replacement therapy (ERT) as well as chaperone therapy aim to reduce intracellular Gb3 accumulation by either replacing the deficient endogenous AGAL or correcting the misfolded endogenous AGAL, with subsequent improvement of trafficking and increased enzymatic activity within the lysosomes. Future therapies such as next-generation ERT or gene therapy aim to diminish present Gb3 content whereas substrate reduction therapies aim to prevent the de novo synthesis of Gb3.

3.1 Enzyme Replacement Therapy (ERT)

First attempts with ERT were carried out in 1973 when Brady and colleagues successfully administered purified human placental AGAL to two FD patients [8]. Both patients tolerated the infusion well and AGAL activity increased about 68% compared to pre-infusion levels [8]. Over the course of time, AGAL obtained from spleen as well as human plasma was administered to two brothers with FD. The administration of plasma-derived AGAL resulted in a Gb3 clearance of up to 70% [9]. Due to the complex purification and insufficient availability of human AGAL for infusion, clinical research progress was limited. However, improved biotechnology processes enabled the production of high amounts of recombinant AGAL protein in cell culture required for appropriate clinical studies. Since 2001, ERT is available as a causal treatment option for FD [10, 11]. The enzyme is administered every 2 weeks as an intravenous infusion (Figs. 2 and 3a). Two preparations in different dosages are currently approved for life-long therapy, including agalsidase-alfa (Replagal, Takeda) produced in a human cell line (human fibrosarcoma cells HT-1080), with an approved dosage of 0.2 mg/kg body weight leading to an infusion duration of approximately 40 min and agalsidase-beta (Fabrazyme, Sanofi Genzyme), which is produced in Chinese hamster ovary (CHO) cells with a recommended dose of 1.0 mg/kg body weight and an infusion duration of approximately 240 min. Depending on individual tolerance, the infusion duration of agalsidase-beta may be progressively reduced to 90 min.

Fig. 2
figure 2

Overview of the ceramide pathway and therapeutic targets of Fabry disease-specific approved and future treatments. AGAL/GLA α-galactosidase A, loss of function results in Fabry disease, A4GALT α-1,4-galactosyltransferase, B3GALNT1 β-1,3-N-acetylgalactosaminyltransferase 1, B4GALT6 β-1,4-galactosyltransferase 6, GBA glucosylceramidase beta, loss of function results in Gaucher disease, GCS glucosylceramide synthase, GLB1 galactosidase-beta 1, loss of function results in GM1 gangliosidosis, HEXA hexosaminidase-subunit alpha, loss of function results in GM2 gangliosidosis

Full size image
Fig. 3
figure 3

Schematic overview of current and future treatment approaches for Fabry disease. a Enzyme replacement therapy. b Migalastat-based chaperone treatment. c Lucerastat- and Venglustat-based substrate reduction therapy. d Lentiviral-based gene correction in haematopoietic stem cells. e Adenoviral-based transduction of liver cells. rhAGAL recombinant human α-galactosidase A, Gb3 globotriaosylceramide, GCS glucosylceramide synthase, ER endoplasmic reticulum, gDNA genomic DNA, mRNA messenger RNA

Full size image

ERT shows good efficacy with stabilization or even improvement of disease load (reviewed in Lenders and Brand [12]) including improvement of quality of life and reducing life-threatening events [13,14,15]. Unfortunately, females with FD are often still untreated despite organ manifestations [16], although an early initiation of therapy is particularly important for the (long-term) success of the therapy in males as well as females [17,18,19,20,21].

Depending on the patients and their manifestations, the following therapeutic effects can be achieved with ERT: Stabilization of kidney function or delay of progression to terminal kidney failure, stabilization of the thickness of the heart wall and function or reduction of left ventricular hypertrophy, relief of neuropathic pain and improvement of gastrointestinal complaints, and improvement in the ability to sweat [12, 20, 22, 23]. With respect to Fabry nephropathy, a dose-dependent reduction of Gb3 inclusions in podocytes was demonstrated in children, suggesting a dose-dependent ERT efficacy with regard to the stabilization of renal function [24,25,26,27,28].

Due to the origin (production) and application of the enzymes, ERT also has limitations resulting in challenges in everyday clinical practice. During infusion, allergic infusion reactions may occur, including cephalia, paresthesia, drop in blood pressure, fever, chills, nausea, and fatigue (especially after infusions). These symptoms can usually be alleviated by reducing the infusion rate and administration of non-steroidal anti-inflammatory drugs, antihistamines, and/or glucocorticoids. More critically, approximately 40% of all males with FD undergoing ERT produce antibodies against the infused enzyme (especially males without endogenous AGAL activity), leading to an inhibition of the infused enzyme, resulting in a worse disease course and poorer outcomes [29, 30]. These neutralizing antidrug antibodies (ADAs) already inhibit the infused enzyme during infusion [31], and impact endothelial enzyme uptake as well as intracellular enzymatic activity [32]. Depending on the titers, higher enzyme doses can compensate for ADAs, but approved dosages limit this approach [31, 33]. So far, no specific immunosuppression approaches in clinical routine have been reported, but in a collective of transplanted male FD patients a suppression of the antibody-mediated ERT inhibition was demonstrated due to immunosuppressive therapy [34]. In this respect, higher immunosuppressive doses were associated with lower antibody titers and a reduced enzyme inhibition [34]. Future studies are needed, aimed at developing ADA-specific immunosuppressive therapy protocols leading to improved disease course in patients with ADAs.

3.2 Chaperone Therapy

Missense mutations within the GLA gene often result in an unstable and misfolded protein, leading to reduced intracellular AGAL activities. Misfolded proteins will not pass the protein quality-control mechanism within the endoplasmic reticulum (ER), resulting in premature degradation before reaching the lysosomes (Fig. 3b) [35, 36]. To restore folding and stability of the protein, pharmacological chaperones can be used, binding reversibly to the active center of the protein [37].

The small molecule 1-deoxygalactonojirimycin (DGJ) is an iminosugar, initially identified as a competitive inhibitor of the AGAL enzyme. At sub-inhibitory concentrations (extracellular: 20–100 µM), the binding to the enzyme’s catalytic center (wild-type and amenable mutations) promotes improved protein folding in the ER as well as accelerated maturation and trafficking to the lysosome [38, 39]. This results in an increase of enzymatic AGAL activity in healthy control cells and (more importantly) in Fabry patient-derived lymphoblasts carrying the first described responsive mutations p.R301Q and p.Q279E [38, 39].

Since May 2016, the pharmacological chaperone migalastat (Galafold; 123 mg hard capsules, every other day; Amicus Therapeutics) is approved as the first oral therapy for FD [40]. For numerous AGAL protein mutants, the addition of migalastat under cell culture conditions (HEK293T cells) leads to a significantly increased enzymatic activity [41]. According to current knowledge, this is based on a reversible binding of migalastat to the active center of the AGAL and, thus, as a consequence of the resulting stabilization, facilitates improved transport to the lysosomes. After uptake of the chaperone enzyme complex into the lysosomes, the small molecule dissociates due to the acidic pH and the lysosomal AGAL concentration increases. As a result of more effective transport, a higher enzyme activity can be achieved in the lysosomes, leading to an improved catabolism of Gb3 (Fig. 2). AGAL mutants showing an increase in enzyme activity after migalastat administration are described as "amenable." The small molecule compound is available for the long-term treatment of adults and adolescents aged 16 years and older with confirmed FD diagnosis and an amenable mutation. The website www.galafoldamenabilitytable.com allows specialists to find out which mutation responds to migalastat in vitro (status as at May 2020: 1384 amenable mutations).

Two phase III studies for treatment with migalastat were conducted. The FACETS study is a placebo-controlled study including treatment-naïve patients (N = 50; 22 placebo vs. 28 migalastat) [42]. The ATTRACT study analyzed the efficacy and safety of migalastat compared to ERT (agalsidase-beta, agalsidase-alfa) in 57 patients (36 migalastat vs. 21 ERT males and females) [43]. The data were promising, since renal function remained stable under a maximum 18-month treatment period with migalastat, a significant reduction of the left ventricular mass index was observed, and plasma lyso-Gb3, as a marker of disease burden, remained low and stable when switching from ERT to migalastat (ATTRACT [43]). An analysis of clinical events related to kidney, heart, and cerebrovascular events and death revealed a frequency of events observed in the migalastat group of 29% and within the ERT group of 44% (p = 0.36) [43]. Overall, migalastat therapy showed good tolerability, with side effects (including ≥ 1/10 headache) not occurring more frequently than with ERT (ATTRACT study) [43]. Although study populations were relatively small and the study duration was limited, the data are of clinical relevance since migalastat does not appear to be inferior to the previous gold standard of ERT. Both phase III studies reported a significant reduction of LVMi (− 7.7 g/m2 and − 6.6 g/m2, respectively) after 24 and 18 months of migalastat-treatment [42, 43]. These data were subsequently confirmed by appropriate “real-world” studies including two single-center studies [44, 45] and one multicenter study [46]. Interestingly, 30 months of data from the open-label extension of the randomized, phase III ATTRACT study demonstrated only a significant reduction of left ventricular mass index (− 10.0 g/m2) in those patients with left ventricular hypertrophy at baseline [47].

Oral therapy with migalastat seems to be a convenient alternative to intravenous ERT for patients with amenable mutations. However, patients with different amenable mutations will show a different clinical response, partly due to the individual increase in AGAL activity, severity of the disease (at treatment initiation), possible comorbidities, and therapy adherence. Recent studies demonstrated that in vitro amenability does not always necessarily correspond to clinical amenability [44, 46, 48]. Some amenable AGAL mutations with low residual activity within the good laboratory practice (GLP)-HEK assay failed to show a biochemical response in appropriate migalastat-treated patients carrying these mutations [46, 48]. For critical mutations in patients lacking clinical amenability, future in-depth analyses including the establishment of CRISPR/Cas9-knockout HEK cells (without endogenous AGAL activity) and/or the investigation of patient-specific cell models will allow a better understanding of the different clinical effectiveness of chaperone therapy of certain mutations [46, 48].

4 Future Treatment

4.1 Next-Generation ERTs

Pegunigalsidase alfa (PRX-102, Protalix Biotherapeutics / Chiesi) is a novel PEGylated (PEG, polyethylene glycol) and covalently cross-linked form of AGAL, developed as ERT for FD and produced in tobacco cells (tobacco plant cell-based ProCellEx System) (Fig. 3a). Pegunigalsidase seems to be equivalent in functionality to the currently available ERTs, with prolonged in vitro stability and a tenfold increase in half-life in male Fabry mice (581 min) compared to approved drugs [49]. A 1-year phase I/II clinical trial (dose-finding study) revealed increased efficacy due to prolonged plasma half-life (80 h) and reduced immunogenicity [50]. The improved half-life (80 h) due to PEGylation, which stabilizes the AGAL homodimer, might allow the infusion interval (monthly intravenous administration) to be extended [51]. Three phase III studies are currently underway (BALANCE [NCT02795676], BRIDGE, and BRIGHT [NCT03180840]). BALANCE is a multicenter, randomized, actively controlled, direct comparison study (head-to-head) to evaluate the safety and efficacy of pegunigalsidase alfa (1 mg/kg) compared to the approved dose of agalsidase beta (1 mg/kg) with a special focus on renal function. BRIDGE is an open switch-over study to assess the safety and efficacy of the switch from an approved dose of agalsidase alfa (0.2 mg/kg) to pegunigalsidase alfa (1 mg/kg). BRIGHT is an open switch-over study to evaluate the safety and efficacy of the switch from an approved dose of agalsidase alfa (0.2 mg/kg) or agalsidase beta (1 mg/kg) every 2 weeks to a higher dose of pegunigalsidase alfa (2.0 mg/kg) every 4 weeks.

Moss-aGal (ELEVA, former Greenovation) is a recombinant human AGAL expressed in Physcomitrella patens, which is a genetically modified moss (Fig. 3a). Preclinical studies suggest an improved uptake of the enzyme by mannose receptors instead of mannose-6-phosphate receptors into cells [52]. A phase I study showed good safety and tolerability of Moss-aGal in six women after a single intravenous dose of 0.2 mg/kg [53]. Phase II and III studies are in preparation.

4.2 Substrate Reduction Therapy

While ERT aims to replace the missing or defective AGAL through the infusion of a genetically engineered enzyme and migalastat increases endogenous enzyme activities of AGAL due to amenable mutations, the aim of a substrate reduction therapy (SRT) is the reduction of the substrate and, therefore, the subsequent inhibition of Gb3 accumulation in the cells (Figs. 2 and 3c). Lucerastat (Idorsia) is a low molecular weight iminosugar inhibiting the upstream-located glucosylceramide synthase (GCS) and, thus, the biosynthesis of glycosphingolipids including downstream Gb3, indicating a potential new oral treatment alternative [54, 55]. The first in vitro studies demonstrated a successful reduction of Gb3 and an amelioration of abnormal cellular membranes in FD patient-derived fibroblasts [54,55,56]. A pivotal phase III study (MODIFY [NCT03425539]) was initiated in 2018 and is still recruiting patients (last updated 24 September 2020).

In addition, Venglustat as a GCS inhibitor demonstrated a favorable safety and tolerability profile (Sanofi Genzyme; NCT01674036; NCT01710826) [57].

4.3 Gene Therapy

Gene therapy is based on the introduction of DNA carrying the genetic code for the AGAL protein into patients’ cells. Using this approach, the causal chain "mutated gene to defective enzyme with defective function to cellular Gb3 deposition in FD patients" would be reached one step earlier compared to ERT (Figs. 2 and 3). Currently, several clinical studies are evaluating the safety of gene therapy for FD, which differ in their therapeutic approaches. The first interventional, multicenter, multinational, open-label study (NCT03454893, NCT02800070, AVR-RD-01, AvroBio) is based on the lentiviral ex vivo transduction of hematopoietic stem cells (Fig. 3d). This approach aims to use transfected hematopoietic stem cell-derived cells as the production platform for functional AGAL production, which will be secreted to the plasma and subsequently internalized by AGAL-deficient cells.

Two further clinical studies (NCT04046224, NCT04040049) [58, 59] are based on adeno-associated viral (AAV) in vivo transduction of hepatocytes, using these cells as an AGAL-secreting platform instead of hematopoietic stem cell-derived cells (Fig. 3e). STAAR is a multicenter, open-label, dose-finding study for the AAV2/6 vector-based drug ST-920 (NCT04046224, Sangamo). The second clinical study on AAV-based gene therapy is also still in the recruitment phase (NCT04040049; FLT190; Freeline Therapeutics). FLT190 is a gene therapy in the test phase, based on a platform that is also developed for the potential future treatment of hemophilia A and B and Gaucher disease. FLT190 consists of a codon-optimized GLA transgene under the control of a liver-specific promoter. The construct, covered by a synthetic capsid, shows improved transduction of human hepatocytes compared to wild-type AAV serotypes [59]. A third clinical study on AAV-based gene therapy is also in the recruitment phase and uses an attenuated AAV (4D-310; 4D Molecular Therapeutics). Preclinical studies in mice demonstrated that the novel capsid 4D-C102 was especially efficient in transducing human cardiomyocytes. Since myocardial cells are hard to reach with ERT, this approach will be of interest for those patients with FD-specific cardiac manifestations.

5 Concomitant Medication

In addition to causal FD treatment, the need for concomitant medication of affected patients is strongly indicated.

5.1 Pain Management

Neuropathic pain often affects the everyday life of many FD patients, significantly lowering quality of life. However, only limited data on the symptomatic treatment of neuropathic pain in FD is available. According to current knowledge, the combination of ERT/migalastat and symptomatic analgesic drugs leads to the most effective pain relief. Even if established drugs are recommended for the treatment of neuropathic pain, some are not advisable due to additional FD-typical manifestations. This includes tricyclic antidepressants, which negatively influence the cardiac conduction system, which is often affected in FD. The effect of non-steroidal anti-inflammatory drugs on neuropathic pain is minimal, so they should be used with caution, especially due to their nephrotoxicity. Current pain-management strategies are based on clinical experience or follow national and international guidelines for the management of neuropathic pain [60,61,62,63]. Tricyclic antidepressants (cave), serotonin and norepinephrine reuptake inhibitors (e.g., duloxetine, venlafaxine), carbamazepine, gabapentin, and pregabalin are considered as first-line options. Lidocaine, topical capsaicin patches, as well as tramadol are considered second-line options; strong opioids should only be considered third-line options [61]. In this respect, the use of controlled-released opioids is preferred over short-acting opioids. Cannabinoids may also be considered as third-line treatments. Finally, methadone (with both N-methyl-d-aspartate and opioid-receptor effects), anticonvulsants with less evidence of efficacy (e.g., lamotrigine and lacosamide), tapentadol, and botulinum toxin are currently considered fourth-line treatments [64]. However, if patients suffer from neuropathic pain, a neurologist with experience in FD should be consulted.

5.2 Reno-Protective Medication

Management of proteinuria is a key feature in preserving renal function in patients with FD. A consistent antiproteinuric therapy with angiotensin-converting enzyme (ACE) inhibitors or angiotensin receptor blockers (ARBs) was shown to decrease the progression of kidney disease in FD [19, 65]. Since a high-sodium diet can diminish the effect of ACE inhibitors and ARBs [66] and is associated with an increased risk of progression to end-stage renal disease in patients with proteinuria [67], a low-sodium diet in FD patients with proteinuria is strongly indicated [68].

5.3 Management of Gastrointestinal Symptoms

Gastrointestinal (GI) symptoms, including postprandial cramping pain, diarrhea, nausea, bloating, and vomiting are typical for patients with FD, especially in those with a classical phenotype. Some major GI symptoms in patients with FD can be treated by various symptomatically effective concomitant drugs. Patients with acute diarrhea can be treated with classical antidiarrheal medication such as loperamide. On the other hand, patients suffering from gastroparesis can benefit from treatments with pro-motility agents such as metoclopramide, which increase the contractile force and accelerate intraluminal transit [69]. Patients suffering from upper GI symptoms may benefit from proton pump inhibitors (e.g., omeprazole) or ondansetron if nausea is present [70]. Medication to combat bloating and flatulence may include the administration of simethicone, which eliminates and prevents foam formation [71, 72]. Furthermore, linaclotide, an oligo-peptide agonist of guanylate cyclase 2C, is used to treat irritable bowel syndrome with constipation and chronic constipation of unknown cause [73, 74]. However, most of these medications are not suitable for long-term use due to side effects. Hence, non-drug-management approaches including dietary modifications (including FODMAP-low diets) or oral AGAL substitution are valuable approaches [75].

6 Unmet Needs

In view of the health economic burden (cost of ERT and chaperone therapy per patient approximately €250,000/year) of a generally lifelong therapy, criteria have to be developed that consider on the one hand the therapy initiation and on the other hand the possible therapy discontinuation (hopeless clinical situation in case of FD progress or newly discovered metastatic tumor disease without foreseeable curative success). It remains to be discussed whether chaperone therapy should be favored for obese patients with an amenable mutation, as this is dosed independently of weight, in contrast to ERT, to avoid additional costs. Ethical aspects have to be considered, which complicate the daily clinical routine for every practitioner. Furthermore, the current therapy has limitations, as deaths occur despite therapy if therapy is started late. Further limitations of ERT are: (1) the short half-life, which results in short therapy intervals; (2) limited accessibility to specific tissues (does not cross the blood-brain barrier); (3) the difficult clearance of clinically relevant renal (podocytes) and cardiac cells (cardiomyocytes) compared to the endothelium; and (4) the high immunogenicity. In this respect, clinicians have not yet developed standards for the management of patients who have limited therapeutic success due to their therapy efficacy-limiting antibodies. To avoid these therapeutic limitations pharmaceutical companies are developing other therapies (gene therapy, SRTs, new ERTs).