Abstract
Atypical hemolytic uremic syndrome (aHUS) is a heterogeneous disorder characterized by microangiopathic hemolytic anemia (MAHA), thrombocytopenia, and acute kidney injury (AKI). In about 50% of cases, pathogenic variants in genes involved in the innate immune response including complement factors complement factor H (CFH), CFI, CFB, C3, and membrane co-factor protein (MCP/CD46) put patients at risk for uncontrolled activation of the alternative complement pathway. As aHUS is characterized by incomplete penetrance and presence of additional triggers for disease manifestation, genetic variant interpretation is challenging and streamlined functional variant evaluation is urgently needed. Here, we report the case of a 27-year-old female without previous medical and family history who presented with confusion, petechial bleeding, and anuric AKI. Kidney biopsy revealed glomerular thrombotic microangiopathy (TMA). Targeted next generation sequencing identified a paternally transmitted novel heterozygous splice site variant in the CFH gene [c.3134-2A>G; p.Asp1045_Thr1053del] which resulted in a partial in-frame deletion of exon 20 transcript as determined by cDNA analysis. On the protein level, the concomitant loss of 9 amino acids in the short consensus repeat (SCR) domains 17 and 18 of CFH includes a highly conserved cysteine residue, which is assumed to be essential for proper structural folding and protein function. Treatment with steroids, plasmapheresis, and the complement inhibitor eculizumab led to complete hematological and clinical remission after several months and stable renal function up to 6 years later. In conclusion, genetic investigation for pathogenic variants and evaluation of their functional impact, in particular in the case of splice site variants, is clinically relevant and enables not only better molecular understanding but helps to guide therapy with complement inhibitors.
Keywords: complement factor H, atypical hemolytic uremic syndrome, splice site variant, short consensus repeat 18, eculizumab, CFH, aHUS
Introduction
Atypical hemolytic uremic syndrome (aHUS; MIM# 235400/612922/612923/612924/615008/612925/612926) is a disease complex characterized by the uncontrolled over-activation of the alternative pathway of the complement system (AP). Clinical symptoms include microangiopathic hemolytic anemia (MAHA), thrombocytopenia, and acute kidney injury (AKI) (Maga et al., 2010). In contrast to the “typical” form of HUS initiated by infection with Shiga-toxigenic Escherichia coli (STEC) and characterized by diarrheal illness (D+), atypical forms (D-) have a poorer prognosis and progress to end-stage renal disease (ESRD) in 30–60% of all cases (Loirat et al., 2008; Westra et al., 2010). Pathogenic variants in AP-regulating genes including CFH, CFI, or MCP/CD46 are found in more than 50% of aHUS-patients and variants in CFH represent the most frequent genetic finding (Fremeaux-Bacchi et al., 2013).
The protein complement factor H (CFH) encoded by CFH plays a key role in the control of complement activation in fluid phase and on cell membranes thereby protecting self-surfaces from immune attacks. It exerts its effects by preventing the formation of the central complement protein C3b from C3 and C5b from C5 by accelerating the decay of C3 and C5 convertases (C3bBb and C3bBbC3b), respectively. Furthermore, it acts as a co-factor of complement factor I (CFI, encoded by CFI) in the proteolytic inactivation of C3b (Figure 1; Merinero et al., 2018).
Complement factor H is a 155 kDa plasma protein that consists of 20 homologous short consensus repeat (SCR) domains of 60 amino acids length, each containing 4 conserved cystein residues that form two structure-defining disulfide-bridges. The region spanning SCR1-4 has been proposed to act as regulatory domain, mediating C3b binding in fluid phase, CFI interaction and convertase decay accelerating activity (Goicoechea de Jorge et al., 2013; Perkins et al., 2014; Clark and Bishop, 2015; de Vriese et al., 2015; Sepúlveda et al., 2016). Whereas SCR6, SCR7, and SCR12-14 seem to be additionally involved in glycosaminoglycan (GAG) or C3b binding, SCR19 and SCR20 predominantly serve as surface-binding domain, comprising the ability to interact with both GAGs and C3b at self-membranes. Therefore, this C-terminal area is assumed to play a key role in distinguishing between host and pathogenic cells. It has been proposed that mutations within the N-terminal part of the protein often result in uncontrolled complement activation in fluid phase leading to glomerulonephritis, whereas C-terminal mutations are more frequently associated with aHUS leading to defects in the recognition and activity at the endogenous endothelia resulting in thrombotic microangiopathy (TMA) (de Vriese et al., 2015). However, the majority of pathogenic CFH variants show incomplete penetrance and constitute predisposing factors lowering the threshold of aHUS/TMA disease manifestation. Upon presence of additional triggers, such as infection, pregnancy, or immunosuppressive drugs, patients with predisposing variants are prone to develop aHUS/TMA. Thus, pathogenic CFH variants are also associated with a significant risk for disease recurrence after renal transplantation. Under these circumstances, complement-targeting therapies (e.g., eculizumab) in addition to the immunosuppressive regimen are able to provide better outcome after renal transplantation in patients with aHUS/TMA (Legendre et al., 2013; Münch et al., 2017). Therefore, genetic testing for pathogenic variants within the AP regulatory genes is indispensable to establish responsible prognosis and treatment strategies, particularly in the context of renal transplantation.
Case Presentation
A 27-year-old female without prior medical and family history presented with nausea, confusion, petechial bleeding, and anuric AKI necessitating admission on intensive care unit and immediate initiation of renal replacement therapy by continuous veno-venous hemofiltration (CVVH). Laboratory examination revealed thrombocytopenia and Coombs-negative hemolytic anemia (hemoglobin 3.7 mmol/L, platelets 118 × 109/L, haptoglobin < 0.1 g/L, fragmented erythrocytes 1%, lactate dehydrogenase > 13 mmol/L) but normal ADAMTS13 levels and activity (>50%) and absence of ADAMTS13 autoantibodies. Complement analysis yielded reduced levels for C3 (0.5 –0.7 g/l; reference range: 0.8 – 1.6) and normal levels for C4. Percutaneous kidney biopsy evidenced signs of acute and non-acute preglomerular and intraglomerular TMA (Figure 2A). The patient was initially treated with intravenous glucocorticoids and 6 weeks of plasma exchange. Only after addition of the C5-inhbitor eculizumab (4 weeks of induction followed by 6 months of maintenance) the patient’s condition slowly resolved with complete hematological and clinical remission, accompanied by gradual recovery of kidney function over several months, allowing to terminate hemodialysis (Figure 2B). Long-term follow up over 6 years showed no relapse and stable renal function at CKD stage 3 (CKD-EPI (Chronic Kidney Disease Epidemiology Collaboration) 40–50 ml/min/1.73 m2) without continued maintenance therapy.
Targeted next-generation sequencing using a gene panel consisting of 14 aHUS-associated genes (including ADAMTS13, C3, CFB, CFD, CFH, CFHR1, CFHR2, CFHR3, CFHR5, CFI, DGKE, MCP, MMACHC, and THBD) identified a novel heterozygous canonical splice site variant in the CFH gene (c.3134-2A>G; NM_000186.3), which was absent from SNP-databases (gnomAD). In addition, the following aHUS-risk alleles were detected: CFH-H3 (heterozygous), MCP-H2 (homozygous), and CFHR1∗B (homozygous). Copy number variations (CNV) of CFH, CFHR1-3 and CFHR5 were excluded by multiplex ligation-dependent probe amplification (MLPA). Segregation analysis yielded paternal transmission despite negative family history. The variant is located within the splice acceptor at the boundary between intron 19 and exon 20 (Figure 3A and Supplementary Figure 1). Sanger sequencing of patient cDNA indicated, that as a consequence of the variant c.3134-2A>G; r.3134_3160del, activation of an intra-exonic splice acceptor site results in an in-frame deletion of the first 27 base pairs of exon 20 transcript (Supplementary Figure 1). On the protein level, the variant leads to a loss of the very C-terminal amino acid of SCR17 and the eight N-terminal amino acids of SCR18 p.Asp1045_Thr1053del (Figure 3B). Importantly, the missing sequence includes Cys1048, which forms one of the two highly conserved intra-domain disulfide bonds with Cys1091 that is thought to be essential for correct domain folding (Figure 3C). In conclusion, this leads to a variant classification as pathogenic according to the American College of Medical Genetics (ACMG) (Richards et al., 2015).
Written informed consent was obtained from the participant for the publication of this report.
Discussion
We here report a novel aHUS-associated CFH splice-site variant [c.3134-2A>G; p.Asp1045_Thr1053del] and predict its potential impact on the protein function by an in-frame deletion of 9 amino acids mainly affecting SCR18 of CFH. Although the activating disease trigger could not be clearly established in this case, we were able to detect the underlying genetic predisposition which allowed us to make the diagnosis of complement-mediated aHUS/TMA. In contrast to non-complement mediated forms (e.g., DGKE, MMACHC), patients with CFH-related aHUS are amenable to treatment with the C5-inhibitor eculizumab.
Complement factor H represents the key regulating protein of the alternative pathway of complement activation, required for fine-tuning of complement activity and differentiation between self-surfaces and pathogenic molecules. Consequently, the majority of pathogenic variants within the CFH gene lead to phenotypes related to disturbed immune processes including aHUS/TMA, C3-glomerulopathy (including dense deposit disease and C3 glomerulonephritis) or age-related macular degeneration (AMD) (Boon et al., 2008; de Córdoba and de Jorge, 2008; Morgan et al., 2012).
To date, a total of 346 disease-associated variants were reported for CFH, 141 of which refer to the phenotypical term “aHUS” (HGMD 2018.4). Of those, the vast majority (76%) represents missense or non-sense variants, whereas indels, complex rearrangements (such as CFH/CFHR1 hybrid genes), and splice site variants account for less than 10% each (Figure 4A). Regarding the domain distribution of the reported missense and non-sense variants, exemplifying variants with known consequences on the protein level, the region spanning SCR19 (total = 22, aHUS-associated = 12) and SCR20 (total = 44, aHUS-associated = 22) clearly represents a mutational hotspot (Figure 4B). Thus, there is emerging evidence for the speculation that variants responsible for the aHUS phenotype might predominantly affect the C-terminal surface recognition domain (de Vriese et al., 2015; Bu et al., 2018).
To effectively allow cell protection, the CFH-molecule has to adopt a U-shaped structure that enables the interaction of its N- and C-terminal domains (SCR 1-4 and SCR19-20) with cell surface-associated C3b and GAG containing recognition sites (Morgan et al., 2012). Previously, it has been shown that SCR18 is connected to SCR19 by a flexible linker, whereas SCR19 and SCR20 are rigidly associated, allowing a kink-like conformational rearrangement of the CFH C-terminal domains with presumably functional implications. To date, six out of 13 known missense and non-sense variants and one of the variants categorized as “small deletion” [c.3269delT; p.(Met1090Serfs∗3)] within SCR18 were reported to be associated with aHUS. In addition, we now identified a pathogenic splice-site variant leading to the deletion of a 9 amino acid sequence mainly located within SCR18. Unfortunately, the majority of newly detected splice-site variants are not routinely subjected to further genetic or functional investigation. Thus, deeper understanding of the disease-causing effects arising from distinct transcript rearrangements remains most often elusive. For CFH, 13 splice-site variants have been described so far (total = IVS 2–6, 8, 16, 18, 19, 21), eight of which were associated with aHUS. Due to the domain-oriented exonic structure of the CFH gene, splice-site variants can affect the previous or the following SCR domain or even lead to a frame-shift resulting in a premature translational stop. The splice-site of intron 19 affected in the patient described here, was already found to be mutated in two previous reports. The variant c.3134-5T>A was found in a genetic screening of a patient cohort known to suffer from renal failure, malignant hypertension, and hypertension-associated TMA (Larsen et al., 2018). Interestingly, this exchange is located only 3bp upstream within the same splice acceptor site and in silico prediction tools (MutationTaster, PolyPhen2 and SIFT) resulted in mixed ratings. Additionally, the variant c.3133+1G>A that is located within the splice donor site of intron 19 was reported in a patient diagnosed with aHUS, however, only in silico analyses (Human Splicing Finder) were conducted suggesting abrogation of the splice donor.
By means of functional analysis, we were able to determine that the defective splice site in our case results in the activation of an intra-exonic splice acceptor, leading to the deletion of an amino acid stretch within SCR18 that contains one of the four conserved cysteine residues of the consensus sequence known to be required for the establishment of the two domain structure-defining disulfide bonds. Loss of these cysteines is highly likely to result in incorrect folding and can be assumed to severely affect protein function. 41 out of 346 total known (12%) and 23 out of 141 aHUS-associated (16%) variants (missense/non-sense) affect a cysteine residue further underlining their obvious functional importance. An accumulation of abrogated cysteine residues was also reported when considering the CFH/ membrane cofactor protein (MCP) consensus sequence (Rodriguez et al., 2014). A defective structural organization of SCR18 probably prevents the required conformational flexibility that is needed for a correct orientation of SCR19 and SCR20 which could negatively affect recognition of interaction partners and host surfaces.
Conclusion
In summary, we detected and analyzed a novel pathogenic CFH splice site variant in a patient with aHUS/TMA, which probably leads to an incorrect protein fold impairing inhibitory control of AP activity. Incomplete penetrance demonstrated by the clinically asymptomatic father underlines the influence of an additional disease trigger for aHUS manifestation. Genetic assessment and functional variant analysis, particularly in the case of detected splice site variants, helps guiding patients’ treatment and assessing the probability of disease recurrence.
Ethics Statement
This study was carried out in accordance with the recommendations of the institutional review board of the University of Leipzig with written informed consent from all subjects. All subjects gave written informed consent in accordance with the Declaration of Helsinki. The protocol was approved by institutional review board of the University of Leipzig.
Author Contributions
RS generated and analyzed the data (genetic) and wrote the manuscript. AS generated the data (clinical) and edited the manuscript. MG generated the data (genetic) and edited the manuscript. TL contributed the clinical data. CB generated the data (genetic) and edited the manuscript. JH initiated and supervised functional evaluation, contributed clinical data, and edited the manuscript.
Funding
JH received funding from DFG (HA 6908/2-1) and EKFS.
Conflict of Interest Statement
MG and CB are employees of Bioscientia/Sonic Healthcare. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Supplementary Material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fgene.2019.00465/full#supplementary-material
References
- Boon C. J., Klevering B. J., Hoyng C. B., Zonneveld-Vrieling M. N., Nabuurs S. B., Blokland E., et al. (2008). Basal laminar drusen caused by compound heterozygous variants in the CFH gene. Am. J. Hum. Genet. 82 516–523. 10.1016/j.ajhg.2007.11.007 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bu F., Zhang Y., Wang K., Borsa N. G., Jones M. B., Taylor A. O., et al. (2018). Genetic Analysis of (400) patients refines understanding and implicates a new gene in atypical hemolytic uremic syndrome. J. Am. Soc. Nephrol. 29 2809–2819. 10.1681/ASN.2018070759 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Clark S. J., Bishop P. N. (2015). Role of Factor H and related proteins in regulating complement activation in the macula, and relevance to age-related macular degeneration. J. Clin. Med. 4 18–31. 10.3390/jcm4010018 [DOI] [PMC free article] [PubMed] [Google Scholar]
- de Córdoba S. R., de Jorge E. G. (2008). Translational mini-review series on complement factor H: genetics and disease associations of human complement factor H. Clin. Exp. Immunol. 151 1–13. 10.1111/j.1365-2249.2007.03552.x [DOI] [PMC free article] [PubMed] [Google Scholar]
- de Vriese A. S., Sethi S., van Praet J., Nath K. A., Fervenza F. C. (2015). Kidney disease caused by dysregulation of the complement alternative pathway: an etiologic approach. J. Am. Soc. Nephrol. 26 2917–2929. 10.1681/ASN.2015020184 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Fremeaux-Bacchi V., Fakhouri F., Garnier A., Bienaimé F., Dragon-Durey M. A., Ngo S., et al. (2013). Genetics and outcome of atypical hemolytic uremic syndrome: a nationwide French series comparing children and adults. Clin. J. Am. Soc. Nephrol. 8 554–562. 10.2215/CJN.04760512 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Goicoechea de Jorge E., Caesar J. J., Malik T. H., Patel M., Colledge M., Johnson S., et al. (2013). Dimerization of complement factor H-related proteins modulates complement activation in vivo. Proc. Natl. Acad. Sci. U.S.A. 110 4685–4690. 10.1073/pnas.1219260110 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Larsen C. P., Wilson J. D., Best-Rocha A., Beggs M. L., Hennigar R. A. (2018). Genetic testing of complement and coagulation pathways in patients with severe hypertension and renal microangiopathy. Modern Pathol. 31 488–494. 10.1038/modpathol.2017.154 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Legendre C. M., Licht C., Muus P., Greenbaum L. A., Babu S., Bedrosian C., et al. (2013). Terminal complement inhibitor eculizumab in atypical hemolytic-uremic syndrome. N. Engl. J. Med. 368 2169–2181. 10.1056/NEJMoa1208981 [DOI] [PubMed] [Google Scholar]
- Loirat C., Noris M., Fremeaux-Bacchi V. (2008). Complement and the atypical hemolytic uremic syndrome in children. Pediatr. Nephrol. 23 1957–1972. 10.1007/s00467-008-0872-4 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Maga T. K., Nishimura C. J., Weaver A. E., Frees K. L., Smith R. J. (2010). Mutations in alternative pathway complement proteins in American patients with atypical hemolytic uremic syndrome. Hum. Mutat. 31 E1445–E1460. 10.1002/humu.21256 [DOI] [PubMed] [Google Scholar]
- Merinero H. M., García S. P., García-Fernández J., Arjona E., Tortajada A., Rodríguez de Córdoba S. (2018). Complete functional characterization of disease-associated genetic variants in the complement factor H gene. Kidney Int. 93 470–481. 10.1016/j.kint.2017.07.015 [DOI] [PubMed] [Google Scholar]
- Morgan H. P., Mertens H. D. T., Guariento M., Schmidt C. Q., Soares D. C., Svergun D. I., et al. (2012). Structural analysis of the C-terminal region (modules 18-20) of complement regulator factor H (FH). PloS One 7:e32187. 10.1371/journal.pone.0032187 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Münch J., Bachmann A., Grohmann M., Mayer C., Kirschfink M., Lindner T. H., et al. (2017). Effective immunosuppressive management with belatacept and eculizumab in post-transplant aHUS due to a homozygous deletion of CFHR1/CFHR3 and the presence of CFH antibodies. Clin. Kidney J. 10 742–746. 10.1093/ckj/sfx053 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Perkins S. J., Fung K. W., Khan S. (2014). Molecular Interactions between complement Factor H and its heparin and heparan sulfate ligands. Front. Immunol. 5:126. 10.3389/fimmu.2014.00126 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Richards S., Aziz N., Bale S., Bick D., Das S., Gastier-Foster J., et al. (2015). Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American college of medical genetics and genomics and the association for molecular pathology. Genet. Med. 17 405–424. 10.1038/gim.2015.30 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rodriguez E., Rallapalli P. M., Osborne A. J., Perkins S. J. (2014). New functional and structural insights from updated mutational databases for complement factor H, Factor I, membrane cofactor protein and C3. Biosci. Rep. 34:e00146. 10.1042/BSR20140117 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sepúlveda R. A., Tagle R., Jara A. (2016). Novel Complement Factor H mutation, a case report of atypical hemolytic uremic syndrome. CRIM 4 263–265. 10.5430/crim.v4n2p13 [DOI] [Google Scholar]
- Westra D., Volokhina E., van der Heijden E., Vos A., Huigen M., Jansen J., et al. (2010). Genetic disorders in complement (regulating) genes in patients with atypical haemolytic uraemic syndrome (aHUS). Nephrol. Dial. Transplant. 25 2195–2202. 10.1093/ndt/gfq010 [DOI] [PubMed] [Google Scholar]
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