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Complement C2 deficiency is the most common genetically determined complete complement deficiency and is associated with a number of diseases. Most prominent are the associations with recurrent serious infections in young children and the development of systemic lupus erythematosus (SLE) in adults. The links with these diseases reflect the important role complement C2 plays in both innate immunity and immune tolerance. Infusions with normal fresh frozen plasma for the treatment of associated disease have demonstrated therapeutic effects but so far protein replacement therapy has not been evaluated.
Human complement C2 was cloned and expressed in a mammalian cell line. The purity of recombinant human C2 (rhC2) was greater than 95% and it was characterized for stability and activity. It was sensitive to C1s cleavage and restored classical complement pathway activity in C2-deficient serum both in a complement activation ELISA and a hemolytic assay. Furthermore, rhC2 could increase C3 fragment deposition on the human pathogen Streptococcus pneumoniae in C2-deficient serum to levels equal to those with normal serum.
Taken together these data suggest that recombinant human C2 can restore classical complement pathway activity and may serve as a potential therapeutic for recurring bacterial infections or SLE in C2-deficient patients.
Our understanding of the role of complement in human disease is the result of numerous studies in recent years focused on complement's mechanism of action. This has resulted in achieving important information on the role of complement as a major mediator and effector mechanism in diseases of immune and non-immune pathogenesis. Complement is not only important for protection against microorganisms, but also contributes to the pathophysiology of a number of autoimmune diseases.
Progress regarding the biological role of complement has been made by studying disease associations in patients with inherited complement protein deficiencies . Genetic deficiencies of complement components are a common denominator of immune and infectious diseases. Deficiencies of complement components of the classical activation pathway, C1, C2 and C4, all lead to increased susceptibility to bacterial infections  and increased risk of developing autoimmune disease, particularly systemic lupus erythematosus (SLE) . The complement system consists of more than 30 soluble and membrane proteins and constitutes an important mediator of host defense against foreign pathogens. Complement component C2 functions as a key regulator in the early activation phase of the classical pathway and participates in the formation of the classical pathway C3 convertase C4b2a . C2 is also a critical component of the lectin pathway. Specifically, when mannose-binding lectin (MBL) or ficolins in complex with MBL-associated serine protease (MASP) molecules bind to relevant carbohydrate molecules, this leads to activation of MASP-2 which then may cleave both C2 and C4 thereby forming the same C3 convertase as in classical pathway activation . Thus, C2 is an important component of both the classical and the lectin pathways of complement activation and is involved in first line defense against microbial infection that is essential for detection and clearance of the invading pathogens .
Complement C2 deficiency is the most common genetically determined complete complement deficiency with a prevalence estimated to be approximately 1:20,000 in individuals of Caucasian ancestry , making it a clinically important immune deficiency . The deficiency is, in the majority of cases, caused by homozygosity for C2 genes having deletions in exon 6, resulting in complete absence of C2, or in some cases caused by other C2 gene mutations [8,9]
The alternative activation pathway, which is C3 dependent, is generally intact in C2 deficiency and can trigger formation of the membrane attack complex (MAC) independently of C2 . However, in the absence of C2, C3 is, in many situations, not efficiently cleaved resulting in a limited deposition of C3 fragments on immune complexes and on the surface of apoptotic cells. Circulating apoptotic cells become a source of self antigen for auto-antibodies that participate in the formation of immune complexes. The immune complexes are deposited throughout the body, potentially causing localized inflammatory reactions in joints and kidneys, and ultimately leading to renal disease from chronic activation of the complement system .
In this study, we considered C2 replacement as a therapeutic target to explore the feasibility of restoring the complement pathway in cases of C2 deficiency. It has been previously proposed that purified human C2 could restore classical and lectin complement pathways and hemolytic activity ex-vivo in serum collected from C2-deficient patients . Two case histories have been described where regular infusions of fresh frozen plasma were beneficial in patients with C2-deficiency and SLE; this benefit was ascribed to the C2 contained in the fresh frozen plasma [12,13]. Therefore, we hypothesized that recombinant human complement component C2 (rhC2) could restore complement activity in serum from C2-deficient patients. To test this hypothesis we have expressed and purified rhC2 and assessed complement activation in vitro. To our knowledge this is the first report of proof of concept for treating C2 deficiency with recombinant human C2.
The rhC2 was highly expressed in human cells and shown to be purified very efficiently by a 2-step column chromatography process (Figure (Figure1A)1A) based on a modification and improvement of a procedure previously described [14,15] (some cleaved products of rhC2, C2a and C2b, are present in the conditioned media as a result of endogenous proteases produced by the cells). After purification, a major band, representing rhC2, is visible by Coomassie staining as well as a smaller band, C2b, the inactive part of the cleaved C2, which co-purifies with the full length protein and constitutes a minor impurity. C2a is completely removed during the purification process. An early report on C2 analysis indicates that the mature protein has eight glycosylation sites . To determine post-translational modification of rhC2 we performed a glycodigestion with Peptide N-glycosidase and show that rhC2 is glycosylated when produced in human cells (Figure (Figure1B).1B). Neuramidase digestion of the protein also demonstrated the presence of sialic acid on rhC2 (Figure (Figure1C),1C), which may result in greater stability of the protein in serum . By multi angle static light scattering (MALS) the weight average molar mass (Mw) of the full length rhC2 including glycosylation was determined to be 99,800 g/mol (Figure (Figure2).2). The number average molar mass (Mn) can also be determined by SEC-MALS, with the ratio Mw/Mn providing a measure of polydispersity. The polydispersity index of rhC2 is 1.00054, indicating narrow mass distribution. The line in figure figure22 represents the differential refractive index (dRI) versus elution time, indicating the elution of rhC2. The data points in figure figure22 are the molar mass determined from the light scattering intensity using the concentration measured by dRI for the glycoprotein complex, and the absorbance at 280 nm for the protein component. The molar mass of the protein component was 84,000 g/mol and the difference in the two masses was the weight of the modifiers (glycosylation) which was 15,800 g/mol. The 84,000 g/mol mass of the protein without any modifiers was consistent with the expected molecular weight calculated from the protein sequence of ~ 82000 kDa. The purity of rhC2 determined by size exclusion chromatography (SEC) was greater than 95% (Figure (Figure3A)3A) with minor impurities consisting mainly of C2b, characterized also by MALDI-TOF analysis (data not shown).
Differential scanning calorimetry (DSC) showed a single temperature induced unfolding transition with a temperature midpoint (Tm) of 53.4°C (Figure (Figure3B).3B). The ratio of the calorimetric enthalpy (ΔHcal) to the van't Hoff enthalpy (ΔHvH) was 2.8, consistent with the three structural domains of rhC2 unfolding in a single transition. Surveys comparing Tm and ΔH at various pH values and salt concentrations indicate that rhC2 is most stable at pH 6.5 and 150 mM NaCl (data not shown).
As a first step in the activation of the classical complement pathway, complement protein C1q binds to antibodies and triggers the activation of C1r and C1s. Activated complement factor C1s cleaves C2 and C4 so they can form the C3 convertase thereby triggering the terminal portion of the complement cascade . Therefore, in order for C2 to be fully functional, it must first be cleaved by C1s. Cleavage of C2 results in release of C2a (70 kDa) which in association with C4b serves as the C3 convertase. A smaller protein, C2b (30 kDa), is also released following cleavage by C1s. To determine that rhC2 exhibited the correct functional conformation, purified protein was incubated with purified C1s and the resultant proteins visualized by SDS-PAGE and Coomassie staining (Figure (Figure4A).4A). Results from these studies show that rhC2 is cleaved by C1s, releasing C2a and C2b proteins of the correct molecular weight. C2 purified from human plasma was included as a positive control. These data suggest that rhC2 forms the correct functional conformation to activate the classical complement pathway.
To determine whether rhC2 was able to restore complement activation through the classical pathway, purified recombinant protein was diluted in affinity depleted C2-deficient serum (0 - 40 μg/ml) and tested using the Total Complement (3-Pathway) ELISA. The 3-pathway ELISA measures the ability of complement proteins in a given serum sample to activate the classical, lectin or alternative pathway based on specific antigens used to trigger each pathway of the cascade. Results show the specific reconstitution of the classical and lectin complement pathways when rhC2 was added to the C2-depleted serum but these pathways were not activated in the absence of rhC2 (Figure (Figure4B).4B). An rhC2 concentration of 3 μg/ml restored > 50% classical pathway activity, with 100% activation at 12 μg/ml. As expected, the alternative pathway, which is independent of C2, was activated by C2-depleted serum. An irrelevant protein (a transferrin fusion protein) with similar MW was used as negative control and did not activate the complement pathway.
Susceptibility to encapsulated bacterial pathogens such as Streptococcus pneumoniae, Neisseria meningitidis and Haemophilus influenzae is a hallmark of C2 deficiency, particularly in young children (≤ 2 years) (2). The classical complement pathway plays a key role in the clearance of these pathogens through antibody and non-antibody-mediated mechanisms. Complement activation by antibodies to encapsulated bacterial pathogens results in the deposition of C3b on the surface of the bacterium in association with C3 cleavage by the C4b2a complex. In the absence of C2, only C4b is bound to the bacterial cells as a result of the classical pathway activation initiated by the specific antibodies. The addition of 25 μg/ml rhC2 or C2 purified from plasma to C2-deficient serum increased the C3d deposition on Streptococcus pneumoniae to levels similar to those using a pool of normal serum (Figure (Figure5A).5A). Thus, we could demonstrate that addition of C2 to C2-deficient serum highly increased the C3 fragment deposition on the bacteria. Figure Figure5B5B shows flow cytometry plot of C3 fragment deposition using a serum sample from a C2-deficient patient serum before and after restitution with rhC2
Considering rhC2 as a therapeutic alternative for C2 deficiency-associated diseases, it was important to test the concept in serum collected from human patients homozygous for C2 deficiency. We have used the 3-pathway ELISA that measures complement cascade activation as well as a hemolytic assay that measures classical pathway activity by determining the ability of serum complement proteins to bind to antibody-coated sheep red blood cells. Successful activation of the classical pathway results in formation of the MAC and red blood cell lysis. Serum from six different C2-deficient patients was reconstituted with rhC2 and tested in the 3-pathway ELISA according to the manufacturer's instructions and three C2-deficient sera were also analyzed by the hemolytic assay . In addition, rhC2 was titrated and tested in C2-deficient serum from patients in the 3-pathway ELISA to investigate the minimum amount of protein needed to restore classical pathway activity to levels similar to those in pooled normal human serum.
Results from the 3-pathway ELISA and hemolytic assay show that rhC2 restores the capacity of C2-deficient patient serum for classical pathway activation enabling the formation of the MAC (Figures (Figures6A6A and and6B).6B). Titration of rhC2 revealed that a concentration of 3.0 - 6.0 μg/ml was sufficient to activate the classical complement pathway to ≥70% activity of normal human serum in different C2-deficient patient sera (Figure (Figure6A).6A). As a reference, normal human serum from healthy individuals contains 16 - 40 μg/ml of circulating C2. No activation of the lectin pathway was observed in most of these patient sera due to low serum levels of MBL (Table (Table11).
In this study we provide proof of concept that rhC2 produced in human cells could be considered as an alternative treatment for C2-deficient diseases. This concept was originally formulated by Ruddy et al , where in an ex-vivo experiment they reconstituted hemolytic activity of C2-deficient serum collected from a patient by adding C2 purified from normal human serum. We have expanded this concept further and have demonstrated that rhC2 can be expressed in high quantities from human cells. We have prepared highly purified rhC2, shown that it undergoes post-translational modification and that it is very stable. rhC2 is cleaved in-vitro by C1s protease generating the active subunit of C2 (C2a) necessary to form the C3 convertase C4b2a and more importantly, it restores the classical and lectin pathways in C2-depleted and C2-deficient serum at different concentrations. The fact that we were able to show normalization of complement activation at concentrations of rhC2 (3-6 μg/mL) that are lower than those typically observed in normal human serum (16-40 μg/mL) is in accordance with the reports that the heterozygous C2-deficiency state is not a risk factor for disease , and confirms that the rhC2 is fully functional.
To our knowledge this is the first report to date describing the production, purification and functional activity of rhC2 produced in human cells. In previous reports C2 was either from plasma of human or animal origin or from mouse L-cells or monkey COS cells [14,19-23]. The advantage of expressing C2 in human cells is that it may result in a more naturally glycosylated protein; most likely very similar or identical to the human C2 secreted in normal individuals, which is, in our opinion, an important consideration for the development of a therapeutic protein. We have also shown that rhC2 restores the classical pathway activation in-vitro in C2-deficient serum obtained from six different patients. The use of C2-deficient human serum represents the proof of concept for therapeutic use of rhC2 as an alternative therapy for C2 deficiency-associated diseases. Restoration of the classical pathway in human C2-deficient serum with rhC2 could be an important step, for instance, in treating C2-deficient SLE patients refractory to current therapies. Interestingly, it has been previously reported in two patients that infusion of normal fresh frozen plasma as a source of complement C2 provided therapeutic benefit [12,13]. Immunological studies performed in one of these patients revealed that these infusions led to increased serum C2 levels, increased hemolytic activity, decreased immune precipitation and decreased circulating immune complexes [13,24]. Although it has been argued that the observed clinical effects of fresh frozen plasma were a result of multiple components in the plasma (Factor B, immunoglobulin, MBL) other than C2, it has been demonstrated that treatment with IgG only in the amount corresponding to one course of plasma infusion  did not have any beneficial effect, suggesting that the key player in promoting complement activity through the classical pathway, was C2 alone. In addition, infusion of rhC2 may decrease the risk of developing adverse reactions compared to plasma infusion as plasma contains many proteins that may trigger different reactions in patients.
The therapeutic use of rhC2 could also be considered in the case of C2-deficient individuals with recurrent or invasive bacterial infections. It has been shown that C2 deficiency is associated with increased susceptibility to recurrent infections by encapsulated bacterial pathogens such as Streptococcus pneumoniae [7,25,26]. Complement activation resulting in opsonization of the bacteria with C3 fragments is an important defense mechanism which is impaired in C2 deficiency . Therefore, we could envision rhC2 as an adjunct therapy to antibiotics, with the rhC2 facilitating phagocyte-mediated clearance of the pathogen by enabling full complement cascade activation.
Blood protein replacement therapy is well established in some clinical situations, for example, intravenous immunoglobulin in patients with antibody deficiencies or coagulation factors in the hemophilias and specific lysosomal hydrolases in lysosomal storage diseases . Drotrecogin alpha, a recombinant form of activated protein C, is approved for use in sepsis and Diffuse Intravascular Coagulation. The only complement replacement therapy already established is in hereditary angioedema caused by C1-inhibitor deficiency. Plasma-derived C1-inhibitor is shown to be an efficient treatment  and recombinant C1-inhibitor is under clinical evaluation . Another complement protein that has been tried as replacement therapy is MBL in patients with MBL deficiency and clinical disease, related to the deficiency. Plasma-derived MBL has been used  and recently recombinant MBL was shown to successfully restore the MBL activation pathway in vivo . Thus, all together these examples suggest that C2 replacement therapy could be considered for further evaluation of possible therapeutic use in humans. Recombinant human proteins offer many benefits over purified products from pooled human plasma, such as a lower risk of transmission of infectious diseases and higher batch-to-batch consistency . Therefore, it was important to show that rhC2 can substitute for endogenously produced C2 in its immune and anti-infective effects. The present report shows that rhC2 is fully functional in vitro and can be considered for protein replacement therapy in C2 deficiency-associated diseases.
We have demonstrated that a biochemically well characterized recombinant human complement component C2 produced in a human cell line restores classical complement pathway activation in vitro, in serum from C2-deficient patients. Establishing efficacy in specific animal models for SLE and infectious diseases will further validate this concept; although the present study provides the first evidence for protein replacement therapy as a treatment of diseases related to C2 deficiency.
Complement component C2 (NM_000063) was cloned from a liver cDNA library (Invitrogen, Carlsbad, CA), and inserted into a plasmid carrying a collagen promoter (pX804) or into pCep4 (Invitrogen, Carlsbad, CA). HT1080 cells (CCL-121, ATCC, Manassas, VA) were grown and maintained in CD media (50% CD-CHO and 50% CD-293) (Invitrogen, Carlsbad, CA) at 37°C in a 5% CO2 incubator. Stable transfections were carried out using electroporation (450 V with 250 μF of capacitance and 30 μg of plasmid DNA suspended in 750 μl 1× PBS). 293-F cells (Invitrogen, Carlsbad, CA) were grown in Freestyle 293 media (Invitrogen, Carlsbad, CA) containing GlutaMAX. Cells were transiently transfected using a polyethylenimine (25 kD, Polysciences, Warrington, PA) to DNA ratio of 3:1 and were supplemented with 2.5 mg/ml Primatone (MP Biomedicals, Solon, OH) at 24 hours. Seventy-two hours after transfection conditioned media enriched in rhC2 was harvested from a 25 liter wave bioreactor (GE Healthcare, Piscataway, NJ) and then processed for purification.
A two-step purification process was developed for rhC2. First a SP Sepharose Fast Flow resin column (GE Healthcare, Piscataway, NJ) was used to capture the protein from harvest medium. The binding capacity of the SP resin was experimentally determined by ELISA to be 0.37 mg rhC2 per ml of SP resin. Protein was then eluted from the column and samples from collected fractions were analyzed by BCA Protein Assay Kit, (Pierce, Rockford, IL) to determine protein concentration and visualized by Coomassie staining (GelCode Blue Stain Reagent, Pierce, Rockford, IL) of 8-16% tris-glycine SDS-PAGE gels under reducing conditions (Invitrogen, Carlsbad, CA). The fractions containing full length rhC2 (102 kDa) were pooled and further purified over a Heparin Sepharose Fast Flow resin column (GE Healthcare, Piscataway, NJ). A binding capacity of 1 mg of total protein by BCA assay per ml of Heparin resin was used. Eluted fractions were assessed as described above and those containing rhC2 were pooled, concentrated and buffer-exchanged into storage buffer (10× PBS diluted to 1× in water and adjusted to pH 7). Forty five liters of harvest media from the WAVE bioreactor yielded 228 mg of purified rhC2. The resultant rhC2 protein was confirmed by N-terminal sequencing (Mayo Proteomics Research Center, Mayo Clinic College of Medicine in Rochester, MN) and was assessed for purity using size exclusion chromatography. Purified rhC2 (5 μg) was separated on a size exclusion chromatography (SEC) column (Tosoh SuperSW 3000, 10,000-500,000 Da, Tosoh, Montgomery, PA) with 25 mM sodium phosphate, pH 6.5 and 500 mM sodium chloride in MilliQ water as the mobile phase with a flow rate of 0.15 ml/min. The chromatogram was quantified using Exponential Skim Integration of the Empower software (Waters, Milford, MA). Using this procedure, the resultant rhC2 was determined to be 96% pure. The molecular weight and hydrodynamic radius of the major peak seen on size exclusion chromatography for rhC2 was analyzed using a multi angle static and dynamic light scattering system from Wyatt Technologies (Santa Barbara, CA) in conjunction with size exclusion chromatography method described above with the following modifications: the pH of the light scattering mobile phase buffer was increased to pH 7.0, the flow rate was increased to 0.3 mL/min, and 10 μg of rhC2 diluted (1:10) in light scattering mobile phase buffer.
Glycodigestion was performed to determine the presence of carbohydrates and sialic acid. Two micrograms of rhC2 was used for glycodigestion, for carbohydrate determination the protein was incubated for 1 hour and overnight at 37°C with Peptide N-glycosidase in reaction buffer (New England Biolabs, Beverly, MA). For sialic acid determination, rhC2 was incubated for 1 hour at 37°C with neuraminidase in reaction buffer (New England Biolabs, Beverly, MA). SDS-PAGE was performed with 250 ng of sample digested with above enzymes, loaded on 8-16% gel and visualized by Western blot. Thermal stability of rhC2 was assessed with differential scanning calorimetry using a MicroCal VP-DSC (GE Healthcare, Piscataway, NJ) with 400 μl buffer (25 mM sodium phosphate, 500 mM sodium chloride) per buffer/sample pairs in 96 deep well plates loaded in the CapVP-DSC autoloader. Data were collected with the calorimeter scanning from 10 to 100°C at a rate of 60°C/hour.
A sandwich ELISA was developed to allow specific quantitation of rhC2 during purification. The wells of a 96-well Nunc Immuno plate (Nalge Nunc International, Rochester, NY) were coated with 100 μl of 1 μg/ml anti-human C2 goat polyclonal antibody (R&D systems, Minneapolis, MN) in 50 mM sodium bicarbonate, pH 9.6. The plate was sealed and incubated overnight at RT. The next morning the wells were washed 3 times with ELISA Wash Buffer (0.1% Tween-20 in PBS), then 300 μl of Blocking Buffer (PBS, 0.05% Tween-20, 2% BSA) were added to each well and the plate was incubated for 1 hour at 37°C. Following the incubation, blocking buffer was removed, 100 μl volume of samples and standards (pre-diluted in blocking buffer) were added to the plate, and the plate was incubated for 1 hour at 37°C. Following incubation, the plate was washed as described above, the secondary antibody, a mouse anti-human C2 monoclonal antibody (Abcam, Cambridge, MA), was added to all wells at a final concentration of 1 μg/mL (100 μl per well) and the plate was incubated for 1 hour at 37°C then washed. After washing, 100 μl of 100 ng/ml of HRP-conjugated anti-mouse antibody (Promega, Madison, WI) was added to each well and the plate was incubated for 1 hour at 37°C then washed. Finally, 100 μl of the complete Peroxidase EIA Substrate Kit (BioRad, Hercules, CA) was added to each well and the plate incubated for 20 min at 37°C. The reaction was stopped by adding 100 μl of 2 N H2SO4 to each well and the plate was read at 450 nm on a Molecular Devices plate reader equipped with SoftMax Pro software. The standard curve had a dynamic range from 200 ng/ml to 3 ng/ml prepared by serially diluting C2 purified from human serum (R&D systems, Minneapolis, MN).
rhC2 and purified C2 from human plasma at a concentration of 25 μg/ml and 50 μg/ml, respectively were incubated with active C1s for 1 h at 37°C in veronal buffered saline with 0.15 mM Ca2+ and 0.5 mM Mg2+ (VBSCaMg) at a concentration of 70 μg/ml to induce complete cleavage of C2. C1s was produced and purified as described by Arlaud G.J. et al, . The proteins were then analyzed by SDS-PAGE using NuPAGE® 4-12% Bis-Tris Gel, NuPAGE MES SDS running buffer (Invitrogen Carlsbad, CA) and visualized by Coomassie staining (Bio-Rad, Hercules, CA).
The activity of purified rhC2 was determined using the Total Complement (3-pathway) ELISA (Alpco, Salem, NH) according to manufacturer instructions. Pooled human serum that had been stripped of C2 by affinity purification (EMD BioSciences, San Diego, CA) was reconstituted with various concentrations of rhC2 and tested. The functional activity of rhC2 was also analyzed by hemolysis in gel assays that detect deficiencies in the classical and alternative pathways of complement activation as well as deficiencies in the terminal sequence. In the classical pathway assay antibody-coated sheep red blood cells were suspended in 0.6% agarose (SeaKemR ME agarose, Cambrex BioScience Rockland Inc., Rockland, ME) in the presence of Ca2+ and Mg2+. Guinea pig erythrocytes in the presence of Mg2+ and EGTA were used similarly in the assay for the alternative pathway. Samples were added to holes punched in the agarose in 5 μl volumes and allowed to diffuse into the agar in moist atmosphere at 4°C for 18 hours and then at 37°C for 2 hours for the lytic reaction to proceed .
Streptococcus pneumoniae 23F, obtained from Statens Serum Institut (Copenhagen, Denmark) were cultured on blood agar plates and then grown in Todd-Hewitt broth until log-phase was reached. The bacteria were harvested, washed in 0.15 M NaCl and killed by adding 0.8% glutaraldehyde in 0.15 M NaCl for 20 min. The killed bacteria were stored in small aliquots at -80°C until use. To measure C3 deposition on the bacteria, serum (100 μl), diluted 1/20 in VBSCaMg, was added to 2.5 μl bacteria and incubated for 30 min at 37°C with continuous agitation. The incubation was stopped by adding 500 μl of ice-cold VBSCaMg. The bacteria were washed (centrifugation 2,880 × g, 15 min) and then 100 μl of anti-C3d (Quidel, Santa Clara, CA), diluted 1/100 in VBSCaMg was added followed by an incubation at 4°C for 30 min. After the incubation the bacteria were washed and resuspended in 100 μl VBSCaMg and 5 μl FITC-conjugated polyclonal F(ab')2 rabbit anti-mouse immunoglobulins (DakoCytomation, Glostrup, Denmark) was added. The tubes were then incubated for 30 min at 4°C. Prior to analysis by flow cytometry (Epics XL-MCL Beckman-Coulter, Fullerton, CA), the bacteria were washed once and resuspended in 500 μl VBSCaMg.
Sera from 6 patients with homozygous C2 deficiency were used. Studies on the C2-deficient patients were approved by the Lund University Research Ethics Committee (LU 513-01) and written informed consent was obtained for each patient. The 6 individuals all had type I C2 deficiency as ascertained by DNA analysis, and had been reported earlier . MBL genotypes had also been determined as reported . Only one of these patients was homozygous for the wild-type variant of the structural MBL2 gene giving rise to high concentration of MBL and lectin pathway activity. The others were heterozygous for this allele and depending on promoter variants they showed lower concentrations of serum MBL to varying degrees.
SLE: systemic lupus erythematosus; C2: complement component C2; rhC2: recombinant human complement component C2; MBL: mannose-binding lectin; MASP: MBL-associated serine protease; MAC: membrane attack complex; MALS: multi angle static light scattering; SEC: size exclusion chromatography; DSC: differential light scattering; PNGase-F: Peptide N-glycosidase-F; MFI: mean fluorescence index.
PGVM wrote the manuscript, AOT, PGVM, LT, JLP, MWH, MFC conceived and designed the experiments, LCC, SA, CB, JG, KJZ, NS, JL produced rhC2 and tested in-vitro, AWN, DML, SMF, KL purified and analyzed rhC2, GJ, CL, BG, LT provided patients serum and performed experiments. All the authors read and approved the final manuscript.
We would like to thank our colleagues at Shire Human Genetic Therapies Inc., Kristin Davis, Kristen Meisner, Nicole Prince, Lisa M. Sturk and in particular Ann J. Barbier for her valuable intellectual contribution to this work.
Project funding was provided by Shire Human Genetic Therapies, Inc.