Recessive SERPING1 Variant Leads to Kinin–Kallikrein System Control Failure in a Consanguineous Brazilian Family with Hereditary Angioedema

Background: Hereditary angioedema (HAE) is a severe and potentially life-threatening disease. The most common forms are caused by variants in SERPING1, resulting in C1-inhibitor (C1-INH) deficiency (HAE-C1-INH). C1-INH is a serine protease inhibitor (SERPIN) that regulates multiple proteases pathways, including the kallikrein–kinin system (KKS) and its complement. In HAE-C1-INH patients, C1-INH deficiencies affect KKS control, resulting in the development of kallikrein activity in plasma and the subsequent release of bradykinin (BK). While the overwhelming majority of disease-causing SERPING1 variants are dominant, very few recessive variants have been described. We present a large Brazilian HAE-C1-INH family with a recessive form of HAE-C1-INH. Methods: Blood samples of family members were investigated for protein levels of C1-INH, C4, C1q, and C1-INH function. The SERPING1 gene was sequenced. Results: In two severely affected sisters, we identified a homozygous missense variant in SERPING1 (NM_000062.3:c.964G>A;p.Val322Met). Fourteen family members were asymptomatic heterozygous carriers of the variant. Data regarding C1-INH function in the plasma showed that homozygous p.Val322Met strongly impacts C1-INH function to inhibit C1s and kallikrein (PKa). When heterozygously expressed, it affects the C1-INH control of C1s more than that of PKa. Conclusions: These studies of the variant’s effects on the structure–function relationship reinforce prior observations suggesting that C1-INH deficiency is a conformational disease.


Introduction
Hereditary angioedema (HAE) is a rare, potentially life-threatening disorder characterized by recurrent episodes of subcutaneous and submucosal edema, often affecting the upper airways, but also the skin and the gastrointestinal tract [1].The worldwide prevalence of HAE has been estimated to be nearly 1/50,000 [2,3].The most common forms of HAE (OMIM #106100), with the acronym HAE-C1-INH, are caused by variants in the SERPING1 gene, leading to a deficiency or dysfunction of the encoded C1-inhibitor (C1-INH) [1].
C1-INH is a highly glycosylated serine protease inhibitor (SERPIN) that regulates different serine proteases via an irreversible suicide substrate mechanism [4,5].It regulates covalent ester linkage between the serine of the protease active site and the backbone carbonyl of the P1 residue.The RCL, located as an exposed and flexible stretch of 15-17 residues tethered between β-sheets A and C, irreversibly inserts into the middle of β-sheet A to give an additional fully antiparallel β-sheet, with removal of the structural constraint as for a native to latent transition.The P15-P9 portion of the RCL is called the hinge region.The region of a SERPIN that controls the opening of β-sheet A and the acceptance of the RCL is the shutter domain.The region of the initial insertion of the RCL is the breach; it is located at the top of the shutter domain.The gate domain assists with this insertion in its open/closed conformations, which are associated with the loss/function of the latch interactions, respectively.The breach, shutter, and gate are the major regions that govern sheet A opening and accept the conserved hinge of the RCL in its insertion into β-sheet A [19]. Figure 1 shows the structural functional domains of C1-INH, with its RCL, breach, shutter, and gate functional regions.
the inhibitory pathway, the proteinase initially forms a noncovalent Michaelis-like complex through interactions with RCL residues, flanking the scissile bond P1-P1′.A metastable conformation is required for SERPIN inhibitory activity, consisting of a conserved secondary structure comprised of β-sheets A, B, and C and at least seven αhelices, from A to I. Considering only intramolecular structural changes, SERPINs can convert to the more stable latent and non-functional species.Attack of the active site serine on the RCL scissile bond leads to a covalent ester linkage between the serine of the protease active site and the backbone carbonyl of the P1 residue.The RCL, located as an exposed and flexible stretch of 15-17 residues tethered between β-sheets A and C, irreversibly inserts into the middle of β-sheet A to give an additional fully antiparallel βsheet, with removal of the structural constraint as for a native to latent transition.The P15-P9 portion of the RCL is called the hinge region.The region of a SERPIN that controls the opening of β-sheet A and the acceptance of the RCL is the shutter domain.The region of the initial insertion of the RCL is the breach; it is located at the top of the shutter domain.The gate domain assists with this insertion in its open/closed conformations, which are associated with the loss/function of the latch interactions, respectively.The breach, shutter, and gate are the major regions that govern sheet A opening and accept the conserved hinge of the RCL in its insertion into β-sheet A [19]. Figure 1 shows the structural functional domains of C1-INH, with its RCL, breach, shutter, and gate functional regions.[20]), presented using PyMOL.The model starts at Phe 122 and lacks a significant part of the N-terminal domain (residues 1-112 of the mature protein).Strategic functional regions [21] are indicated as follows: (i) the reactive site loop (RCL) at the top of the picture, colored light blue, including Arg 466 P1 and the hinge region (P15-P9), essential for protease recognition and RCL mobility, undergoing a conformational transformation for its insertion as strand 4A (s4A); that is, S > R transition after protease inhibition; (ii) the central β-sheet A, colored red, with the breach region located at its top, serving as a point of initial insertion of the RCL, and the shutter domain, situated close to the center of β-sheet A, which, along with the breach, assists in sheet opening and accepts the insertion of the conserved proximal hinge s4A between s3A and s5A; (iii) the gate, including s3C and s4C of β sheet C. β-sheets B and C are at the top of the model, colored green and brown, respectively.Picture drawn by Dr. Christine Gaboriaud, Grenoble.
More than 800 pathogenic HAE-correlated SERPING1 variants have been reported [22], and the vast majority of them are inherited in a dominant fashion and represent missense, nonsense, or frameshift variants with a dominant negative effect [23].Approximately 6% of the variants occur de novo [10].In contrast with a large spectrum of dominant variants, only very few recessive forms of HAE-C1-INH have been described in a limited number of families [10,[24][25][26][27][28][29][30][31].All the recessive variants are located in exonic regions and result in HAE-1 in the majority of patients.
In the present study, we analysed the SERPING1 gene in a large Brazilian fourgeneration family and identified a novel SERPING1 variant acting in a recessive fashion.We discuss the implications of the altered protein for the manifestations of symptoms in this family.

Subjects
We investigated a consanguine Brazilian four-generation family, including 23 women and 11 men aged between 1 and 81 years (Figure 2).Two sisters presented clinical symptoms of HAE and fulfilled the diagnostic criteria for HAE-1.The age of symptom onset in the affected women was 13 years (index) and 26 years (sister).Both of the sisters showed subcutaneous edema, abdominal pain, and oropharyngeal and laryngeal attacks.The index patient was diagnosed at 47 years of age.She did not have any prodrome.She had intense edema attacks occurring approximately three times a month in the subcutaneous, upper airway, and abdominal tracts.Her sister also was given the HAE late diagnosis at the age of 52 years.The symptoms were very frequent, with four episodes per month.She had prodromes 2-24 h before the edema and could correlate the edema with anxiety and stress or menses.In both sisters, the symptoms stopped after treatment with oxandrolone.

Severity Score
Disease severity was assessed using previously reported scores.The Bygum sc focused on the age of onset, number of organs affected, and need for long-te prophylaxis [32].The Ferraro score focused on the frequency and intensity of angioede attacks and scaled the severity from asymptomatic to severe (mild and moderate) [ (Table S1).

Levels of C1-INH, C4 and C1q
Citrate plasma samples from the individuals were prepared by centrifugating fres collected blood at 2000× g for 10 min to harvest the platelet-free plasma.The samples w immediately aliquoted and stored at −80 °C until use for testing of C1-INH function.

Severity Score
Disease severity was assessed using previously reported scores.The Bygum score focused on the age of onset, number of organs affected, and need for long-term prophylaxis [32].The Ferraro score focused on the frequency and intensity of angioedema attacks and scaled the severity from asymptomatic to severe (mild and moderate) [33] (Table S1).

Levels of C1-INH, C4 and C1q
Citrate plasma samples from the individuals were prepared by centrifugating freshly collected blood at 2000× g for 10 min to harvest the platelet-free plasma.The samples were immediately aliquoted and stored at −80 • C until use for testing of C1-INH function.
The serum protein levels of C1-INH, C4, and C1q were measured using radial immunodiffusion.The reference intervals (5th-95th percentiles) for the C1-INH levels are between 195 and 345 mg/L (men/women), and for C4, they are between 162 and 445 mg/L (men) or 167 and 385 mg/L (women).The normal C1q levels range between 118 and 238 mg/L (men) or between 118 and 244 mg/L (women).

Functional Studies
Analysis of C1-INH function is the key laboratory test used to make a diagnosis of HAE-C1-INH.A C1-INH functional analysis was performed on the citrate plasma samples using chromogenic assays of the residual enzyme activity.These assays involved using a commercial kit with C1s protease (Technochrom ® C1-INH assay, Illkirch, France) or using kallikrein (PKa) as target, as described by Ghannam et al. [8].Briefly, KKS was reconstituted using the purified components (FXIIa, plasma prekallikrein, and high-molecular-weight kininogen, (Enzyme research, Swansea, UK)) and was either submitted or not submitted (reference control) to incubation with a C1-INH standard (positive control) or plasma sample.The kinetics of the amidase activity, which is increased in HAE patients, were monitored using Pro-Phe-Arg-pNA (Proteogenix, Schiltigheim, France), independently of alpha2-macroglobulin control of KKS.
Functional levels are considered normal when they are ≥50% (men/women) and ≥0.61 or ≥0.42 IU/mL for men and women, respectively, using C1s protease and PKa as targets.

Identification of C1-INH Species
The C1-INH-HAE type was characterized based on the distribution of C1-INH molecular species before and after a 15-min incubation of plasma sample in the presence or absence of target protease (1.5:1, protease:C1-INH ratio).Briefly after, both samples were submitted to 7.5% sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) under non-reducing conditions, followed by transfer onto an Immobilon-P ® polyvinylidene difluoride membrane (MilliporeSigma, Bedford, MA, USA) and submitted to anti-C1-INH immunoblotting (HRP-labeled sheep polyclonal anti-C1-INH antibody; The Binding Site, Grenoble, France).After incubation with Clarity Western ECL Blotting Substrate ® (BioRad, Paris, France), the bands were quantified using a ChemiDoc ® imaging system (BioRad) and distinguished between the 105 kDa native or latent form, the 180 kDa C1-INH-protease association, and the 95 kDa cleaved form with reference to a molecular ladder.

Genetic Studies
Genomic DNA was extracted from the EDTA whole blood (adults) using a DNA Wizard Genomic DNA Purification Kit (Promega, Madison, WI, USA), and from the oral mucosa (children) using a QIAamp DNA Blood Mini Kit ® (Qiagen, Hilden, Germany).PCR and Sanger sequencing were performed for the index patient and core family using primers for the coding region of SERPING1, as previously described [35].For all other DNA, exon 6 of SERPING1 was sequenced.The genomic DNA sequences were analyzed using the Mutation Survey or SeqMan software ® Version 17 (Soft Genetics LLC Lasergene; DNA Star, Inc., Madison, WI, USA).Sequence variants were identified through comparisons with GenBank accession number NG_009625.1.The significance of the variant was predicted using various tools (EVE, CADD PHRED, Mutation Taster, PolyPhen-2, and SIFT).

Ethical Considerations
The present study was approved by the Ethics Committee of the Clinical Hospital of Ribeirão Preto Medical School (HCRP Protocol No. 6583/2016, on 29 February 2016) and conducted according to the Helsinki guidelines.All the patients or their legal guardians provided written informed consent to participate in this study.

Severity of Disease
The clinical severity scores of the two homozygous individuals classified them as severely affected (Bygum score: 7 and 6; Ferraro score: for both 8).Careful clinical reexamination of the heterozygous individuals excluded any HAE symptoms.

Biochemical Studies
The homozygous patients showed markedly reduced C1-INH function using both C1s protease and PKa as targets, with residual activities measuring less than 20% of the control capacity for C1s and less than 12.9% of the control for PKa activity (Table 1).Their serum samples also displayed a significant decrease in antigenic C1-INH and C4, with a normal antigenic C1q, excluding a diagnosis of acquired C1-INH deficiency using anti-C1-INH autoantibodies.The heterozygous patients showed a 30-50% decrease in antigenic C1-INH, associated (three individuals) or not (five individuals) with decreased antigenic C4, and a 10-40% decrease in the C1-INH control capacity of C1s; however, the control of PKa was within or very close to the normal values.The spontaneous PKa activity was increased and the proenzyme activatability was decreased in the samples from the homozygous individuals, but they were nearly normal in those from the heterozygous individuals (Figure 2 and Table 1).These data are in line with a decreased control of PKa by the p.Val322Met variant in the homozygous carriers.

Studies of C1-INH Molecular Species
Anti-C1-INH immunoblot assays of the samples from the heterozygous individuals showed a faint band at 180 KDa, corresponding to the C1-INH-protease complex, which was undetectable in the samples from the homozygous individuals.This indicates that p.Val322Met was unable to establish a normal covalent bridge between serpin and the C1s protease.Two bands of 95 KDa and 105 KDa were displayed with comparable intensity for the samples submitted (+C1s) or not (−C1s) to the C1s protease when compared between both homozygous and heterozygous carriers.The observation of an apparent absence of serpin protease association with an abundance of both remnant 105 KDa and cleaved 95 KDa species in the (+C1s) samples indicates a low susceptibility of cleavage of p.Val322Met and quasi-impossible ester bonding with C1s, with an expression of both the wild type and variant in the heterozygous individuals (Figure 3).This profile is consistent with an expression of the p.Val322Met variant and is characteristic of an HAE-C1-INH of the intermediate type.absence of serpin protease association with an abundance of both remnant 105 KDa and cleaved 95 KDa species in the (+C1s) samples indicates a low susceptibility of cleavage of p.Val322Met and quasi-impossible ester bonding with C1s, with an expression of both the wild type and variant in the heterozygous individuals (Figure 3).This profile is consistent with an expression of the p.Val322Met variant and is characteristic of an HAE-C1-INH of the intermediate type.

Genetic Studies
Sanger sequencing of all coding exons of the SERPING1 gene revealed a homozygous missense variant in the index patient and in her symptomatic sister (c.964G>A,p.Val322Met) that was not listed in gnomAD.Fourteen individuals of the family were identified to be asymptomatic heterozygous carriers of the same variant, and eighteen individuals presented the wild type sequence in exon 6.No other variants were identified in the gene.

Discussion
In the present study, we investigated a large consanguineous Brazilian family presenting with a clinical phenotype and biological characteristics of HAE-C1-INH and identified a novel variant in the SERPING1 gene (c.964G>A,p.Val322Met) that was recessively inherited in the HAE-C1-INH-affected individuals.This variant fits into a

Genetic Studies
Sanger sequencing of all coding exons of the SERPING1 gene revealed a homozygous missense variant in the index patient and in her symptomatic sister (c.964G>A,p.Val322Met) that was not listed in gnomAD.Fourteen individuals of the family were identified to be asymptomatic heterozygous carriers of the same variant, and eighteen individuals presented the wild type sequence in exon 6.No other variants were identified in the gene.

Discussion
In the present study, we investigated a large consanguineous Brazilian family presenting with a clinical phenotype and biological characteristics of HAE-C1-INH and identified a novel variant in the SERPING1 gene (c.964G>A,p.Val322Met) that was recessively inherited in the HAE-C1-INH-affected individuals.This variant fits into a small series of recessive variants that are distributed across the complete SERPING1 gene (Figure S1).Previous studies have reported eight families with homozygous or compound heterozygous probands and an unambiguous recessive form of HAE-C1-INH [10,[24][25][26][27][28][29][30][31] (Table S2).The recurrent variant c.1198C>T (p.Arg400Cys), rs201363394, which was identified in five kindreds, actually appears to be a dominant variant, because several symptomatic heterozygous carriers were identified [8,[36][37][38].It has been shown that the p.Arg400Cys protein is secreted on a decreased level as an active, although quite unstable, monomer.However, it could bear a folding defect, occasionally promoting protein oligomerization and interfering with the secretion process, thus accounting for its plasma level variability.This defect is exacerbated by the nature of the mutation, since the acquired cysteine leads to the formation of non-functional homodimers through inter-molecular disulfide bonding.All the proposed phenomena could be modulated by specific environmental conditions, rendering this mutant exceptionally vulnerable to mild stress [36].Clear evidence of c.1198C>T as a recessive variant comes from the observation of a Spanish family, with a highly symptomatic homozygous carrier, expression of the variant product in serum, and the absence of HAE-C1-INH-related symptomatology in heterozygous individuals [28].
The various prediction tools that we used to predict the pathogenic effect showed a heterogeneous picture (Table S2).This reflects the challenges in classifying the functional effects of recessive variants based on limited biological data.Interestingly, two variants affecting the same codon, p.Val322Glu and p.Val322Gly, showed a dominant inheritance pattern [10,39], and at least for one of them (p.Val322Glu), it was shown that the variant resulted in an intermediate HAE phenotype [10].
Testing of C1-INH function is the "gold standard" for the diagnosis and treatment of HAE-C1-INH.It has been established through the conventional spectrophotometric assay using C1s protease as the target, and the method is recommended for its high sensitivity for diagnostic of C1-INH deficiency [40].However, the measurement is based on the residual activity of the C1s protease, which is not involved in the pathological process itself.For this reason, we developed an alternative enzymatic assay of C1-INH function based on KKS activation, i.e., control of PKa, which directly corresponds to the control of the pathological kinin-forming pathway.This method has been evaluated and aligned with angioedema diagnostic requirements [7,8].The use of this method is of particular strategic importance for the investigation of the present family, where variant p.Val322Met does not similarly affect both C1s protease and KKS, as shown for the homozygous patients.
Interestingly, when we take into account the "gold standard" data from biochemical analyses of C1-INH function and antigenic C1-INH as diagnostic parameters [12,15], we would clearly expect a symptomatic phenotype in heterozygous carriers of the p.Val322Met variant.The homozygous patients presented with a low C1-INH antigenic level and function, as well as low antigenic C4, in line with HAE-C1-INH characteristics, whereas the heterozygous individuals showed subnormal to normal C1-INH parameters and normal antigenic C4.This indicates that C4 consumption did not occur above a threshold of C1s protease control by C1-INH.The heterozygous carriers of other recessive variants also displayed this feature, which could therefore be characteristic of a C1-INH deficiency associated with a recessive variant.Nevertheless, it should be emphasized that a low antigenic C4 has been shown to be inconsistent in a proportion of HAE-C1-INH patients [41].Moreover, low antigenic C4 is not uncommon in healthy individuals; for example, those carrying one or two C4AQo or C4BQo alleles.For this reason, we do not recommend antigenic C4 for HAE-C1-INH biological testing.
Approximately 85% of patients with HAE-C1-INH are classified as HAE-1, and 15% are classified as HAE-2 [2,15].The overlap between the elementary biochemical characteristics of HAE-1 and the intermediate type can also be seen in the present family, complicating the correct classification and potentially leading to misclassification [10].Nonetheless, with its structure-function relationship, the identification of an intermediate type for a new variant confers an additional criterion supporting the pathogenicity in ACMG criteria [42].
Adding the analyses of C1-INH function to the control of PKa contributes to explaining the asymptomatic status of heterozygous carriers, because those values were within normal range, although they were borderline in some samples.In contrast, the homozygous individuals showed much lower PKa-correlated values, which is in accordance with homozygous individuals with other reported recessive SERPING1 variants [22,24].Our data indicate that the disrupting effect of C1-INH on the control of KKS, correlated with very high spontaneous PKa activity (Table 1), is of greater importance for the development of symptomatic HAE than that of the complement.Whether this is true for all carriers of a recessive variant needs to be clarified in follow-up studies.Our results clearly underline the importance of functional studies on C1-INH in combination with standard analyses on data curation to identify the pathogenicity of SERPING1 variants.Future studies on C1-INH in other recessive families will help to understand the functional protease specificity of the protein.
In contrast to HAE-2-correlated variants that are often localized within the RCL region of the protein (70% of type 2 variants), the recessive variants do not affect this specific region of the protein, but are instead distributed across different gene regions.Val 322 is a highly conserved position among serpins (80%), located within a buried hydrophobic environment in sheet-3C.Together with the variants at positions Phe 313 (sheet-4C), Ser 318 (sheet-3C), and Met 325 (sheet-3C), Val 322 is one of the few residues that are involved in the gate functional region.It packs against conserved gate positions at sheet-4C (Phe 313 ), -3C (Met 324 ), -2C (Pro 399 ), and the distal hinge (Pro 498 ) in native C1-INH.All these positions are also highly conserved among serpins and are affected by dominant missense pathogenic variants.Regarding the identified missense variant p.Val322Met, the Val to Met transition suggests a modified hydrophobicity and disruption of the insertion capacity of the cleaved RCL sequence into the A-sheet [10].Subsequently, this feature explains a reduced C1-INH function and is in line with an absence of serpin-protease association, as shown in Figure 3.
The treatment of both homozygous sisters with oxandrolone improved the clinical phenotype.This effect is most likely attributable to an increase in the expression of aminopeptidase P, a metallo-peptidase of bradykinin catabolism.Aminopeptidase P levels are known to be increased in HAE-C1-INH patients submitted to danazol prophylaxis compared to patients without prophylaxis, and aminopeptidase P activity showed a significant inverse relationship to disease severity (p ≤ 0.001) [43].

Conclusions
The identified c.964G>A (p.Val322Met) variant exhibits a modified structure conformation with subsequent functional changes in the gate region of C1-INH.This suggests that C1-INH deficiency should be considered as a conformational disease.Biochemical analyses of standard laboratory measurements of antigenic C1-INH and antigenic C4 in asymptomatic heterozygous carriers of the recessive variant p.Val322Met would suggest a symptomatic phenotype.These individuals, however, do not show clinical symptoms.We assume that, in these individuals, the normal function of C1-INH towards the control of PKa might explain their asymptomatic status.An anti-C1-INH immunoblot analysis showed that p.Val322Met is not capable of establishing a covalent association between serpin and C1s protease, in accordance with the hypothesis of a low accessibility of p.Val322Met to target proteases and a disrupted function of the gate domain.
Data of further asymptomatic heterozygous SERPING1 variant carriers could improve our knowledge of strategic amino acids that are crucial for particular functional domains of C1-INH, i.e., gate, breach, and shutter.

Figure 1 .Figure 1 .
Figure 1.Overall structure of the native C1-INH serpin domain, with crucial regions ascribed to C1-INH serpin function.The positions of the following variants are shown: p.Val322Met, in front of the picture and in the middle of the gate; Gln223, which could participate in the shutter; Leu349, within the breach functional domain; Ile401, participating in the gate; and Ser460 and Ile462, as P7 and P5 of the RCL, respectively.The Arg400 position is protruding behind the picture.Five regions for the serpin function are presented in the 3D model of C1-INH (PDB ID 5DU3; [20]), presented using PyMOL.The model starts at Phe122 and lacks a significant part of the N-terminal domain (residues 1-112 of the mature protein).Strategic functional regions [21] are indicated as follows: (i) the reactive Figure 1.Overall structure of the native C1-INH serpin domain, with crucial regions ascribed to C1-INH serpin function.The positions of the following variants are shown: p.Val322Met, in front of the picture and in the middle of the gate; Gln 223 , which could participate in the shutter; Leu 349 , within the breach functional domain; Ile 401 , participating in the gate; and Ser 460 and Ile 462 , as P7 and P5 of the RCL, respectively.The Arg 400 position is protruding behind the picture.Five regions for the serpin function are presented in the 3D model of C1-INH (PDB ID 5DU3; [20]), presented using PyMOL.The model starts at Phe 122 and lacks a significant part of the N-terminal domain (residues 1-112 of the mature protein).Strategic functional regions [21] are indicated as follows: (i) the reactive site loop (RCL) at the top of the picture, colored light blue, including Arg 466 P1 and the hinge region (P15-P9), essential for protease recognition and RCL mobility, undergoing a conformational transformation for its insertion as strand 4A (s4A); that is, S > R transition after protease inhibition; (ii) the central β-sheet A, colored red, with the breach region located at its top, serving as a point of initial insertion of the RCL, and the shutter domain, situated close to the center of β-sheet A, which, along with the breach, assists in sheet opening and accepts the insertion of the conserved proximal hinge s4A between s3A and s5A; (iii) the gate, including s3C and s4C of β sheet C. β-sheets B and C are at the top of the model, colored green and brown, respectively.Picture drawn by Dr. Christine Gaboriaud, Grenoble.

Figure 2 .
Figure 2. Pedigree of the family with recessive HAE-C1-INH.Homozygous individuals are mar with a solid color (+/+), and heterozygous individuals (+/−) and wild type individuals (−/−) indicated without colors.The numbers representing biochemically examined individuals are lar and highlighted in bold.

Figure 2 .
Figure 2. Pedigree of the family with recessive HAE-C1-INH.Homozygous individuals are marked with a solid color (+/+), and heterozygous individuals (+/−) and wild type individuals (−/−) are indicated without colors.The numbers representing biochemically examined individuals are larger and highlighted in bold.

Figure 3 .
Figure 3. Circulating C1-INH molecular species demonstrated using an anti-C1-INH immunoblot.Plasma samples were collected from patients presenting with HAE-C1-INH, regardless of whether they were experiencing an attack or remission period.The plasma samples were incubated with C1s protease at 37° C for 15 min and were then submitted to SDS-PAGE analysis.The 180 KDa band corresponds to the C1INH protease complex, the 105 KDa band corresponds to to native C1-INH, and the 95 KDa band corresponds to cleaved C1-INH species.Ctrl, sample from a healthy donor.

Figure 3 .
Figure 3. Circulating C1-INH molecular species demonstrated using an anti-C1-INH immunoblot.Plasma samples were collected from patients presenting with HAE-C1-INH, regardless of whether they were experiencing an attack or remission period.The plasma samples were incubated with C1s protease at 37 • C for 15 min and were then submitted to SDS-PAGE analysis.The 180 KDa band corresponds to the C1INH protease complex, the 105 KDa band corresponds to to native C1-INH, and the 95 KDa band corresponds to cleaved C1-INH species.Ctrl, sample from a healthy donor.

Table 1 .
Laboratory characteristics of the HAE patients and their relatives.Whereas the values for antigenic C1-INH, C1-INH function, and antigenic C4 are below normal for homozygous and heterozygous carriers of the c.964G>A, p.Val322Met variant, this only applies for the homozygous carrier (II.3;II.4) in case of the PKa activity.Arrows indicate values below the 5th quantile (↓) or above the 95th quantile (↑), which are indicated in bold.Reference intervals are given below the table.