Next Article in Journal
Programmed Cell Death-1: Programmed Cell Death-Ligand 1 Interaction Protects Human Cardiomyocytes Against T-Cell Mediated Inflammation and Apoptosis Response In Vitro
Next Article in Special Issue
Recent Strategic Advances in CFTR Drug Discovery: An Overview
Previous Article in Journal
Treatment of Delirium in Older Persons: What We Should Not Do!
Previous Article in Special Issue
TMEM16A: An Alternative Approach to Restoring Airway Anion Secretion in Cystic Fibrosis?
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
IJMS
Volume 21
Issue 7
10.3390/ijms21072398
ijms-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Treatment of Cystic Fibrosis Patients Homozygous for F508del with Lumacaftor-Ivacaftor (Orkambi®) Restores Defective CFTR Channel Function in Circulating Mononuclear Cells

by
Maria Favia
1,
Crescenzio Gallo
2,
Lorenzo Guerra
1,
Domenica De Venuto
3,
Anna Diana
4,
Angela Maria Polizzi
4,
Pasqualina Montemurro
5,
Maria Addolorata Mariggiò
5,
Giuseppina Leonetti
3,
Antonio Manca
3,
Valeria Casavola
1 and
Massimo Conese
6,*
1
Department of Biosciences, Biotechnologies and Biopharmaceutics, University of Bari, 70125 Bari, Italy
2
Department of Clinical and Experimental Medicine, University of Foggia, 71122 Foggia, Italy
3
Cystic Fibrosis Regional Center, Department of Biomedical and Human Oncology, Pediatrics Section, U.O. “B. Trambusti”, Policlinico, University of Bari, 70124 Bari, Italy
4
UOC Laboratorio di Genetica Medica, Department of Biomedical and Human Oncology, Policlinico, University of Bari, 70124 Bari, Italy
5
Department of Biomedical Sciences and Human Oncology, Section of General Pathology, University of Bari, 70124 Bari, Italy
6
Department of Medical and Surgical Sciences, University of Foggia, 71122 Foggia, Italy
*
Author to whom correspondence should be addressed.
Int. J. Mol. Sci. 2020, 21(7), 2398; https://0-doi-org.brum.beds.ac.uk/10.3390/ijms21072398
Submission received: 13 February 2020 / Revised: 13 March 2020 / Accepted: 25 March 2020 / Published: 31 March 2020
(This article belongs to the Special Issue Therapeutic Approaches for Cystic Fibrosis)
Browse Figures
Versions Notes

Abstract

:
The treatment of cystic fibrosis (CF) patients homozygous for the F508del mutation with Orkambi®, a combination of a corrector (lumacaftor) and a potentiator (ivacaftor) of the mutated CFTR protein, resulted in some amelioration of the respiratory function. However, a great variability in the clinical response was also observed. The aim of this study was to evaluate the response to Orkambi® in a small cohort of F508del/F508del patients (n = 14) in terms of clinical and laboratory parameters, including ex vivo CFTR activity in mononuclear cells (MNCs), during a 12-month treatment. Patients responded with an increase in percent predicted forced expiratory volume in 1 s (FEV1%) and body mass index (BMI) as well as with a decrease in white blood cell (WBC) total counts and serum C-reactive protein (CRP) levels, although not significantly. Sweat chloride and CFTR-dependent chloride efflux were found to decrease and increase, respectively, as compared with pre-therapy values. CFTR and BMI showed a statistically significant correlation during Orkambi® treatment. Clustering analysis showed that CFTR, BMI, sweat chloride, FEV1%, and WBC were strongly associated. These data support the notion that CFTR-dependent chloride efflux in MNCs should be investigated as a sensitive outcome measure of Orkambi® treatment in CF patients.

1. Introduction

Cystic fibrosis (CF) is an autosomal recessive disorder due to mutations occurring in the CFTR (CF Transmembrane Conductance Regulator) gene, encoding for a chloride-conducting channel located at the apical membrane of epithelial cells. The lack/dysfunction of the CFTR protein leads to progressive fat and vitamin malabsorption and failure to thrive, abnormal salt concentration in sweat, and progressive lung failure due to infection by opportunistic pathogens and mucosal chronic inflammation [1].
CFTR is a glycosylated protein that functions as a chloride channel regulated by cAMP and protein kinase A (PKA)-mediated phosphorylation [2]. In normal cells, after passing the endoplasmic reticulum quality control, CFTR is translocated to the Golgi complex where it is fully glycosylated and subsequently transported and inserted into the apical membrane of polarized cells, where it is subjected to endocytosis and then recycled to the plasma membrane or targeted for lysosomal degradation [3,4,5]. The most frequent CFTR mutation leads to the deletion of phenylalanine at position 508 of CFTR (F508del), resulting in a folding defect and premature degradation by the ubiquitin-proteasome system [6,7,8]. Consequently, in the respiratory system of patients affected by CF, there is a defective Cl− secretion, a NaCl hyperabsorption, a depletion of airway surface liquid, and a secondary failure of mucociliary clearance [9] associated with an exaggerated immune response and impairment of lung function [10].
The pharmacological corrector VX-809 (now lumacaftor) was found to interact directly with the MSD1 domain of CFTR and partially rescue the functional expression of F508del-CFTR to the cell surface in heterologous expression systems [11,12,13]. Together with the potentiator VX-770 (now ivacaftor), a drug that facilitates the opening of the F508del-CFTR channel present on the plasma membrane channel activity [14], lumacaftor has been found to enhance the functional activity of F508del-CFTR in pre-clinical studies conducted on primary bronchial cell cultures and rectal biopsy-derived organoids [11,15]. In 2015, the U.S. FDA approved ivacaftor-lumacaftor (Orkambi®) for the use in patients 12 years of age or older and homozygous for the F508del CFTR mutation [16]. Orkambi® treatment has been demonstrated to be associated with an improvement in pulmonary function and reduction in respiratory exacerbations and its use was recently extended to include those 6–11 years old [17]. The monitoring of treatment in 1030 patients up to 96 weeks has revealed that Orkambi® is safe and allows for a prolonged slower rate of FEV1 decline than in matched registry controls [18]. However, while Orkambi® therapy influences different factors, such as the F508del- CFTR stability or the mucociliary clearance [19,20], it is associated with variable clinical responsiveness [21] suggesting that its efficacy may differ according to the patients’ conditions, including genetics. These findings highlight the importance of finding new biomarkers predictive of an individual patient’s response.
In the search of novel and non-invasive biomarkers, which should be predictive of the therapeutic response in CF patients, we recently demonstrated [22] that human peripheral blood monocytes (MNCs) isolated from CF patients treated with ivacaftor could represent an important tool for the analysis of CFTR-dependent chloride efflux rescue and to evaluate the therapeutic response in CF patients. Furthermore, the correlation between MNC chloride efflux with FVC and FEV1 indicates that this test could be a surrogate marker similar to the respiratory function parameters. In this study, we sought to demonstrate that the treatment combination ivacaftor-lumacaftor (Orkambi®) was able to correct the CFTR-dependent chloride efflux in CF people homozygous for F508del. Overall, the data presented in this study support the notion that CFTR-dependent chloride efflux in MNCs should be investigated as a sensitive outcome measure of Orkambi® treatment in CF patients.

2. Results

2.1. Clinical Monitoring during Orkambi® Treatment

We recruited fourteen CF patients homozygous for the F508del mutation and variable lung disease as judged from FEV1% predicted (FEV1%). At the baseline (pre-therapy), these patients were characterized by high sweat chloride and high CRP levels, and were underweight (Table 1). They were also characterized by systemic inflammatory response (i.e., high CRP).
Follow-up of these patients was at 1, 6, and 12 months of Orkambi® treatment. Figure 1 depicts the changes of clinical parameters in time. Compared with starting levels (122.9 ± 3.2 mEq/L (mean ± SEM)), sweat chloride showed a decreasing trend over time, with a significant difference at six months (p < 0.05), while BMI and FEV1% increased in time, although only by trend. In particular, BMI increased from 20.4 ± 0.6 to 21.7 ± 0.6 Kg/m2, and FEV1% from 59.3 ± 7.5 to 68.1 ± 7.3, as comparing baseline to 12 months of treatment. CRP decreased only after 12 months of treatment (5.9 ± 2.3 mg/dL) as compared with the pre-treatment values (7.3 ± 1.6 mg/dL), although not significantly.
To evaluate a systemic effect of Orkambi® on marrow-derived peripheral cells, the total number of platelets as well as white blood cells (WBC) and percentages of different cell populations were evaluated (Figure 2). Platelet counts did not show any substantial changes in time. WBC counts decreased at one month post-treatment and stabilized from six months onward. Neutrophils followed the same trend. Eosinophils and basophils increased at one month post-treatment, but while eosinophils returned to pre-treatment values, basophils were higher than baseline also at longer times. Finally, while monocytes peaked at six months post-treatment and then decreased to pre-treatment levels, lymphocytes increased at one month of treatment and remained at these levels up to 12 months. None of these changes were significant.
An extension study was conducted on clinical and laboratory parameters by enlarging the analyses to 20 other patients homozygous for F508del taking Orkambi® as additional therapy and thus obtaining a total of 34 CF patients. All parameters confirmed the trend observed with only 14 patients, however none of these changes was significant (Table S1).

2.2. Effect of the Treatment with Orkambi® on CFTR-Dependent Chloride Efflux and Protein in MNCs

In the cohort of 14 patients, we analyzed whether treatment with Orkambi® could influence CFTR-dependent chloride efflux in circulating MNCs. CFTR-dependent chloride efflux was analyzed by spectrofluorimetric analysis using the chloride-sensitive dye, MQAE, following a procedure that we developed [22]. The experimental conditions for the CFTR functional assay was established with MNCs obtained from healthy subjects. Briefly, chloride efflux rate after substitution of chloride by nitrate in the perfusion medium was measured by the change in fluorescence (∆(F/F0)/min) of MQAE. Stimulation of PKA by addition of FSK plus IBMX increased chloride efflux in MNCs. The addition of the CFTR specific inhibitor, CFTRinh-172 (5 µM), before and during the next stimulus inhibited this increase to basal levels, confirming the specificity of the effect on CFTR-mediated anion transport. CFTR-dependent chloride efflux is defined as the difference between the rate of FSK plus IBMX-stimulated chloride efflux in the absence and presence of CFTRinh-172 treatment.
Treatment with Orkambi® increased CFTR-mediated chloride efflux in all patients, although they responded differently (Figure S1). As shown in Figure 3A, CFTR-dependent chloride efflux was not detectable in MNCs prior to treatment, in line with our previously published data [23]. Cumulative data show that the CFTR-dependent chloride efflux in MNCs was significantly increased at 6 (0.0130 ± 0.0019 ∆(F/F0)/min) and 12 months (0.0126 ± 0.0015 ∆(F/F0)/min) post-treatment, although still being lower than observed in non-CF MNCs (0.0187 ± 0.0022 ∆(F/F0)/min, n = 6).
We then determined the effect of Orkambi® treatment on the expression/maturation of F508del- CFTR protein. As shown in Figure 3B, in the MNCs pool derived from healthy subjects (n = 5), wt CFTR was expressed as the fully glycosylated mature form of the protein (Band C) migrating at 180 kDa and the core glycosylated form, Band B (160 kDa). Importantly, while before Orkambi® treatment the CF patient-derived MNCs expressed only a barely detectable immature band B of F508del-CFTR, after 6 and 12 months of treatment, there was an increase in the expression also of the mature band C of F508del CFTR protein (Figure 3B). Densitometric analysis revealed that Orkambi® treatment resulted in a significant increase of Band C in CF MNCs at 6 and 12 months and that the CFTR protein amount at 12 months was similar to that of non-CF MNCs (Figure 3C).

2.3. Correlation among the Clinical Parameters and CFTR Activity

To determine whether the parameters were correlated with each other during Orkambi® treatment, we performed a correlation analysis of the parameters’ behavior over treatment time, considering the average value of each parameter on all patients. A representation of interrelation of the variables with each other demonstrated that CFTR correlated with BMI, WBC, FEV1, and sweat chloride (Figure 4A). Only the correlation of CFTR activity with BMI was significant (r = 0.97; p < 0.05). WBC strongly correlated with sweat chloride (r = 0.98; p < 0.05). Figure 4A also shows that, while lymphocytes correlated positively with basophils and eosinophils, they strongly negatively correlated only with neutrophils (r = −0.99; p < 0.01). Platelets and eosinophils correlated positively (r = 0.98; p < 0.05). Monocytes and CRP correlated with low statistical significance.
From the above correlations, we can highlight three well-defined groups (Figure 4B): (i) CFTR activity, FEV1, sweat chloride, WBC, and BMI; (ii) platelets, neutrophils, lymphocytes, basophils, and eosinophils; and (iii) CRP and monocytes.

3. Discussion

The effects of CFTR modulators on pulmonary function, pulmonary exacerbations, sweat chloride concentration, and quality of life have been well documented, whereas less evidence is available on extrapulmonary manifestations, including inflammation and immunity [24]. A few studies have shown that ivacaftor increases innate immune cell activities, such as killing of P. aeruginosa by neutrophils and monocytes [25,26] and oxidative burst of neutrophils as mediated by enhanced expression of hydrogen voltage-gated channel-1 [22]. Interestingly, ivacaftor-lumacaftor (Orkambi®) treatment was not associated with improved phagocytosis and killing of P. aeruginosa by monocyte-derived macrophages [26]. Others have reported a decreased neutrophil–epithelial cell binding (which may prelude to decreased diapedesis) [27], while a proteomic analysis of monocytes from patients treated with ivacaftor showed a decrease in the expression of markers that mediate migration and response to interferon-γ [28].
As a novel biomarker for therapeutic efficacy in CF patients focused on immune cells, we investigated if and how CFTR-dependent chloride channel activity in MNCs was modified by ivacaftor in the past [22] and by Orkambi® in the present study. Ivacaftor treatment of patients harboring non-G551D gating mutations was associated with a significant increase in MNC CFTR channel activity and this response was paralleled by a decrease in sweat chloride concentration [22]. In the present study, CFTR channel activity increased significantly after 6 and 12 months of treatment with Orkambi® of F508del/F508del patients while sweat chloride showed a significant decrease only at 6 months. Although the cohort of patients in both studies is very small (seven patients with ivacaftor and fourteen with Orkambi®), together with previously reported studies, it is tempting to speculate that CFTR modulators have variable effects depending on class mutation or on the extent to which the CFTR modulator increases CFTR activity. Importantly, in both studies, the only significant variations were observed for in vivo and ex vivo parameters determined directly by CFTR activity (sweat chloride and chloride channel in MNCs). Recently, it has been shown that complex alleles comprising F508del and an exonic variant (F87L-I1027T) can affect the increase in FEV1 in patients treated with Orkambi® and the rescue of CFTR activity by lumacaftor in in vitro experiments [21]. Unfortunately, the number of patients in our study with a complex allele (i.e., with the mutation A238V in cis) was only n = 2 and this hampered the possibility to draw any strong appraisal of its effect on CFTR activity in MNCs.
While in the previous study with ivacaftor treatment, chloride MNC positively correlated with FEV1 and FVC [22], in the present study, MNC CFTR activity correlated with BMI. Two phase 3 randomized clinical trials (TRAFFIC and TRANSPORT) investigated the comparative safety and efficacy of Orkambi® in patients with CF who were 12 years old and older with mild to moderate lung disease and who were homozygous for the F508del-CFTR mutation [29]. Both studies demonstrated that 24 weeks of treatment with Orkambi® was associated with statistically significant improvements in FEV1% predicted (absolute increases of 2.6–3.0% and relative increases of 4.3–4.5%); however, the magnitude of improvement in respiratory function is uncertain but may be clinically relevant for CF patients, given that changes in FEV1% have been shown to be correlated with mortality [30]. An ongoing extension study (PROGRESS) demonstrated that the improvements in FEV1% persisted after 48 weeks of treatment [18]. In this study, the absolute increase in FEV1% at 12 months (i.e., 48 weeks) was 8.9%, making this improvement higher than in previous clinical trials, although not significant as compared to pre-therapy values, likely because we dealt with 14 patients instead of hundreds in phase 3 studies. To see if an increase in patients’ number could yield a different result, we extended the analyses of clinical parameters to 20 other patients, however resulting in no statistically significant changes. Our cohort of 34 patients comprises subjects with a broad respiratory function at the baseline (from 21 to 118 FEV1%), and this may constitute a big difference with phase 3 studies, in which patients were initially excluded if their baseline lung function (FEV1%) was less than 40%, as also has been observed in a recent observational study [31]. Again, this consideration indicates conducting observational studies in a higher number of patients with more homogenous clinical status. Nevertheless, a real-world trial on severe CF patients has shown that about one third of all patients enrolled to receive Orkambi® had an absolute change in FEV1% of 5% or more in comparison to baseline and 13% had an increase of at least 10% in FEV1% [32], indicating that Orkambi® treatment may result in beneficial effects on lung function comparable to those reported in clinical trials in patients with less severe lung disease, as in our study. Results for change from baseline in BMI and weight gain were inconsistent with statistically significant improvements observed in TRANSPORT but not in TRAFFIC studies [29]. A pre-planned pooled analysis, however, suggests that treatment with Orkambi® was associated with improvements in BMI, although the magnitude of improvement was of uncertain clinical significance [29]. Here, we picked up a positive correlation with BMI that was confirmed by the clustering analysis in which we found that CFTR activity in MNCs composed a sub-group that included BMI, FEV1%, sweat chloride, and WBC, suggesting that this ex vivo activity related to CFTR is a variable that explains some in vivo features related to the respiratory function, sweat gland function, body growth, and inflammation.
It has been shown that CFTR dysfunction is associated with a slowing of inflammation resolution and an altered bacterial killing [33,34,35,36]. Whether our results showing the recovery of CFTR function in circulating MNCs upon Orkambi® treatment is reflected by a protective behavior of monocytes/macrophages in the CF lung will be the objective of future studies.
In conclusion, our real-life study suggests CFTR activity in circulating mononuclear cells as an interesting surrogate biomarker of the adjunctive therapy of CF patients with Orkambi®. In particular, young CF patients who typically have both mild disease and poorly standardized outcome measure may benefit from the development of more sensitive disease biomarkers.

4. Patients and Methods

4.1. Patients

All patients enrolled in this study were homozygous for the F508del mutation and had a confirmed diagnosis of CF [23]. The first cohort of 14 patients was comprised of people ≥12 years old (5 females, 9 males). These patients commenced Orkambi® at the median age of 23.5 years (range 13–45 years). Two patients also had the A238V mutation in cis [24]. Twenty other patients (14 females, 6 males) were also treated with Orkambi® and included in this study (median age of 16.5 years; range 6–32 years). Two out of 20 also had the A238V mutation in cis. At the first dose of Orkambi®, all patients were pancreatic insufficient. Overall, sixteen patients were colonized in the airways by Staphylococcus aureus, 13 by Pseudomonas aeruginosa, 9 by Candida albicans, 4 by Stenotrophomonas maltophilia, 2 by Enterobacter cloachae, 1 by Klebsiella pneumoniae, 1 by Klebsiella oxytoca, 1 by Candida lusitanae, 1 by Achromobacter xylosoxidans, 1 by Nocardia, and 1 by Burkholderia cepacia. Patients enrolled in this study took two capsules of Orkambi® every 12 h (each capsule containing 200 mg of lumacaftor and 125 mg of ivacaftor) in association with 20 g of fat. All the other medications were not discontinued. At baseline (pre-therapy) and at 1, 6, and 12 months of treatment the following outcome measures were considered: sweat chloride (mEq/L), FEV1%, body mass index (BMI; kg/m2), C-reactive protein (CRP; mg/dL), platelets (n/mm3), white blood cells (WBC; n/mm3), neutrophils (% of WBC), basophils (% of WBC), eosinophils (% of WBC), lymphocytes (% of WBC), and monocytes (% of WBC). Moreover, CFTR-dependent chloride efflux in mononuclear cells (MNCs) was considered.
The study was approved by the ethics committee of the Azienda Ospedaliera Universitaria “Policlinico” of Bari, Italy (No. 999/CE/08/01/2016) and performed in accordance with the 1964 Declaration of Helsinki. Written informed consent from the adult study subjects or written consent from the next of kin, caretakers, or guardians on behalf of the enrolled children was obtained.

4.2. Isolation of Blood Mononuclear Cells

Heparin anti-coagulated blood was obtained from the 14 CF patients in accordance with the ethical guidelines. Briefly, peripheral blood mononuclear cells were isolated from dextran sedimentation followed by Ficoll-Hypaque (GE Healthcare, Little Chalfont, UK) density gradient centrifugation. The upper plasma layer was aspired and the middle phase containing mononuclear cells was collected and washed in RPMI 1640 medium (Aurogene, Roma, Italy). Viability of the cells was determined by Trypan Blue dye extrusion and resulted in ≥98% viable MNCs.

4.3. CFTR Function Measurement in Mononuclear Cells

First, 4 × 105 freshly isolated mononuclear cells (MNC), seeded on 0.1% poly-l-lysine coated glass coverslips, were loaded overnight in culture medium containing 5 mM N-(ethoxycarbonylmethyl)-6-methoxyquinolinium bromide (MQAE) at 37 °C in a CO2 incubator. Fluorescence was recorded with a Cary Eclipse Varian spectrofluorometer. To measure chloride efflux rate across the plasma membrane, the perfusion medium was changed with a medium in which chloride was substituted with iso-osmotic nitrate as previously described by us [22]. All experiments were performed at 37 °C in HEPES-buffered bicarbonate-free media, Cl− medium (in mM: 135 NaCl, 3 KCl, 1.8 CaCl2, 0.8 MgSO4, 20 HEPES, 1 KH2PO4, and 11 glucose) and Cl- free medium (in mM: 135 NaNO3, 3 KNO3, 0.8 MgSO4, 1 KH2PO4, 20 HEPES, 5 Ca(NO3)2, and 11 glucose). At the end of each experiment, a two-point calibration procedure was performed: the maximal intensity of fluorescence (F0) was determined by perfusing the cells with the Cl− free medium; the minimal fluorescence was obtained by exposing the cells to a solution containing (in mM) 110 KSCN, 1 MgSO4, 10 HEPES, 1 CaSO4, 5 glucose, and 0.005 valinomycin. The rate of chloride efflux induced by treatment with forskolin plus IBMX (3-isobutyl-1-methylxanthine) after substitution of chloride by nitrate in the perfusion medium was measured by the change in fluorescence of MQAE. CFTR-dependent chloride efflux was calculated as the difference in alterations of FSK stimulated fluorescence in the absence and presence of CFTR selective inhibitor CFTRinh-172 (5 µM).

4.4. Western Blot of CFTR in MNCs

Protein extraction from mononuclear cells was performed essentially as described previously [23]. In total, 5 × 106 MNCs were lysed in ice-cold buffer (pH 8.0) containing 50 mM NaCl, 50 mM Tris, 1 mM EDTA, 1% Triton X-100, 0.1 mM Na-Vanadate, 0.5 mM dithiothreitol, 0.5 mM phenylmethylsulfonyl fluoride, and 10 µL/mL of protease inhibitor cocktail (Sigma-Aldrich, Milan, Italy). Lysates were frozen overnight at −80 °C, and then cleared by centrifugation (22,000 g, 20 min, 4 °C).
Supernatants were collected and assayed for protein concentration using the Micro BCA Protein Assay kit (ThermoFisher Scientific, Monza, Italy). Equivalent amounts of protein (usually 20 µg) were supplemented with sample buffer (1.5 M Tris, pH 6.8) containing 56% sucrose, 14% SDS, 1.4% β-mercaptoethanol, and 0.02% bromophenol blue, and separated using a 4–12% polyacrylamide gel (Bio-Rad Laboratories, Milan, Italy). The gel was transferred to PVDF membranes Millipore (Merk Life Science, Milan, Italy) and processed for Western blotting by using monoclonal CFTR antibody (dilution 1:500; clone: 24–218 1, MAB25031 R&D Systems, Minneapolis, MN, USA) and anti-mouse HRP-conjugated secondary antibody. Immunocomplexes were detected with Pierce ECL plus reagent (ThermoFisher Scientific, Rodano (Milan), Italy) and image processing was carried out using Adobe Photoshop and the Image software package (version 1.61, National Institutes of Health, Bethesda, MD, USA). As the housekeeping proteins themselves were variably expressed, the total lane density of transferred proteins on the membrane stained with Ponceau red was used for the normalization of proteins. Due to limited amount of MNC, CFTR protein analysis was carried out only in three CF patients.

4.5. Statistical analysis

The initial dataset was composed of four-stage recordings (pre-therapy, 1 month, 6 months, and 12 months) for 14 patients and for each of the 12 parameters detected (WBC, neutrophils, lymphocytes, monocytes, basophils, eosinophils, platelets, CRP, FEV1%, BMI, sweat chloride, and CFTR activity). The missing data (less than 3% of the total) were imputed with the average of the values present for each parameter.
The initial detail values of the 14 patients were then summarized with the averages of the patient records for each of the 4 times and 12 parameters, for a total of 48 final values. A descriptive statistical analysis was performed on this dataset, which showed an almost always normal distribution of values for the parameters. To compute the p-values, analysis of variance with post-hoc Tukey test was used. Then, the Pearson’s correlation coefficient matrix among the 12 parameters was calculated (see the equivalent correlation graph shown in Figure 4A). After establishing a threshold of 0.65, all links (and their nodes) with a coefficient lower than the threshold were removed from the correlation graph. On the remaining subgraph, a clustering analysis was carried out (by means of the method of modularity maximization) identifying three communities of parameters (with a greater number of connections between the vertexes of the same community and relatively few that unite the vertexes of different communities), which are illustrated in Figure 4B.

Supplementary Materials

Supplementary Materials can be found at https://0-www-mdpi-com.brum.beds.ac.uk/1422-0067/21/7/2398/s1.

Author Contributions

Conceptualization, M.F., L.G., P.M., M.A.M., V.C., and M.C.; Data curation, C.G., D.D.V., A.D., A.M.P., and G.L.; Formal analysis, C.G. and M.C.; Investigation, M.F., L.G., D.D.V., A.D., A.M.P., G.L., and A.M.; Methodology, M.F. and C.G.; Writing—original draft, M.C.; and Writing—review and editing, C.G., P.M., M.A.M., V.C., and M.C. All authors have read and agreed to the published version of the manuscript.

Funding

This work was supported by the Italian Ministry of Health (Law 548/93).

Conflicts of Interest

The authors declare no conflict of interest.

Abbreviations

CFTRCystic fibrosis transmembrane conductance regulator
BMIBody mass index
CRPC-reactive protein
FEV1Forced expiratory volume in 1 s

References

  1. Ratjen, F.; Bell, S.C.; Rowe, S.M.; Goss, C.H.; Quittner, A.L.; Bush, A. Cystic fibrosis. Nat. Rev. Dis. Primers 2015, 1, 15010. [Google Scholar] [CrossRef] [PubMed]
  2. Rowe, S.M.; Miller, S.; Sorscher, E.J. Cystic fibrosis. N. Engl. J. Med. 2005, 352, 1992–2001. [Google Scholar] [CrossRef] [PubMed]
  3. Gentzsch, M.; Chang, X.B.; Cui, L.; Wu, Y.; Ozols, V.V.; Choudhury, A.; Pagano, R.E.; Riordan, J.R. Endocytic trafficking routes of wild type and DeltaF508 cystic fibrosis transmembrane conductance regulator. Mol. Biol. Cell 2004, 15, 2684–2696. [Google Scholar] [CrossRef] [PubMed]
  4. Sharma, M.; Pampinella, F.; Nemes, C.; Benharouga, M.; So, J.; Du, K.; Bache, K.G.; Papsin, B.; Zerangue, N.; Stenmark, H.; et al. Misfolding diverts CFTR from recycling to degradation: Quality control at early endosomes. J. Cell Biol. 2004, 164, 923–933. [Google Scholar] [CrossRef] [Green Version]
  5. Lukacs, G.L.; Segal, G.; Kartner, N.; Grinstein, S.; Zhang, F. Constitutive internalization of cystic fibrosis transmembrane conductance regulator occurs via clathrin-dependent endocytosis and is regulated by protein phosphorylation. Biochem. J. 1997, 328 Pt 2, 353–361. [Google Scholar] [CrossRef] [Green Version]
  6. Denning, G.M.; Ostedgaard, L.S.; Welsh, M.J. Abnormal localization of cystic fibrosis transmembrane conductance regulator in prymary cultures of cystic fibrosis airway epithelia. J. Cell Biol. 1992, 118, 551–559. [Google Scholar] [CrossRef] [Green Version]
  7. Du, K.; Sharma, M.; Lukacs, G.L. The DeltaF508 cystic fibrosis mutation impairs domain-domain interactions and arrests post-translational folding of CFTR. Nat. Struct. Mol. Biol. 2005, 12, 17–25. [Google Scholar] [CrossRef]
  8. Turnbull, E.L.; Rosser, M.F.; Cyr, D.M. The role of the UPS in cystic fibrosis. BMC Biochem. 2007, 8 (Suppl. S1), S11. [Google Scholar] [CrossRef] [Green Version]
  9. Knowles, M.R.; Boucher, R.C. Mucus clearance as a primary innate defense mechanism for mammalian airways. J. Clin. Investig. 2002, 109, 571–577. [Google Scholar] [CrossRef]
  10. Boucher, R.C. Cystic fibrosis: A disease of vulnerability to airway surface dehydration. Trends Mol. Med. 2007, 13, 231–240. [Google Scholar] [CrossRef]
  11. Van Goor, F.; Hadida, S.; Grootenhuis, P.D.; Burton, B.; Stack, J.H.; Straley, K.S.; Decker, C.J.; Miller, M.; McCartney, J.; Olson, E.R.; et al. Correction of the F508del-CFTR protein processing defect in vitro by the investigational drug VX-809. Proc. Natl. Acad. Sci. USA 2011, 108, 18843–18848. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  12. Eckford, P.D.; Ramjeesingh, M.; Molinski, S.; Pasyk, S.; Dekkers, J.F.; Li, C.; Ahmadi, S.; Ip, W.; Chung, T.E.; Du, K.; et al. VX-809 and related corrector compounds exhibit secondary activity stabilizing active F508del-CFTR after its partial rescue to the cell surface. Chem. Biol. 2014, 21, 666–678. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  13. Ren, H.Y.; Grove, D.E.; De La Rosa, O.; Houck, S.A.; Sopha, P.; Van Goor, F.; Hoffman, B.J.; Cyr, D.M. VX-809 corrects folding defects in cystic fibrosis transmembrane conductance regulator protein through action on membrane-spanning domain 1. Mol. Biol. Cell 2013, 24, 3016–3024. [Google Scholar] [CrossRef] [PubMed]
  14. Van Goor, F.; Hadida, S.; Grootenhuis, P.D.; Burton, B.; Cao, D.; Neuberger, T.; Turnbull, A.; Singh, A.; Joubran, J.; Hazlewood, A.; et al. Rescue of CF airway epithelial cell function in vitro by a CFTR potentiator, VX-770. Proc. Natl. Acad. Sci. USA 2009, 106, 18825–18830. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  15. Dekkers, J.F.; Berkers, G.; Kruisselbrink, E.; Vonk, A.; de Jonge, H.R.; Janssens, H.M.; Bronsveld, I.; van de Graaf, E.A.; Nieuwenhuis, E.E.; Houwen, R.H.; et al. Characterizing responses to CFTR-modulating drugs using rectal organoids derived from subjects with cystic fibrosis. Sci. Transl. Med. 2016, 8, 344ra384. [Google Scholar] [CrossRef] [PubMed]
  16. Wahlgren, N.; Moreira, T.; Michel, P.; Steiner, T.; Jansen, O.; Cognard, C.; Mattle, H.P.; van Zwam, W.; Holmin, S.; Tatlisumak, T.; et al. Mechanical thrombectomy in acute ischemic stroke: Consensus statement by ESO-Karolinska Stroke Update 2014/2015, supported by ESO, ESMINT, ESNR and EAN. Int. J. Stroke 2016, 11, 134–147. [Google Scholar] [CrossRef] [Green Version]
  17. Milla, C.E.; Ratjen, F.; Marigowda, G.; Liu, F.; Waltz, D.; Rosenfeld, M.; VX13-809-011 Part B Investigator Group. Lumacaftor/ivacaftor in patients aged 6–11 years with cystic fibrosis and homozygous for F508del-CFTR. Am. J. Respir. Crit. Care Med. 2017, 195, 912–920. [Google Scholar] [CrossRef] [Green Version]
  18. Konstan, M.W.; McKone, E.F.; Moss, R.B.; Marigowda, G.; Tian, S.; Waltz, D.; Huang, X.; Lubarsky, B.; Rubin, J.; Millar, S.J.; et al. Assessment of safety and efficacy of long-term treatment with combination lumacaftor and ivacaftor therapy in patients with cystic fibrosis homozygous for the F508del-CFTR mutation (PROGRESS): A phase 3, extension study. Lancet Respir. Med. 2017, 5, 107–118. [Google Scholar] [CrossRef]
  19. Cholon, D.M.; Quinney, N.L.; Fulcher, M.L.; Esther, C.R., Jr.; Das, J.; Dokholyan, N.V.; Randell, S.H.; Boucher, R.C.; Gentzsch, M. Potentiator ivacaftor abrogates pharmacological correction of DeltaF508 CFTR in cystic fibrosis. Sci. Transl. Med. 2014, 6, 246ra296. [Google Scholar] [CrossRef] [Green Version]
  20. Meng, X.; Wang, Y.; Wang, X.; Wrennall, J.A.; Rimington, T.L.; Li, H.; Cai, Z.; Ford, R.C.; Sheppard, D.N. Two small molecules restore stability to a subpopulation of the cystic fibrosis transmembrane conductance regulator with the predominant disease-causing mutation. J. Biol. Chem. 2017, 292, 3706–3719. [Google Scholar] [CrossRef] [Green Version]
  21. Masson, A.; Schneider-Futschik, E.K.; Baatallah, N.; Nguyen-Khoa, T.; Girodon, E.; Hatton, A.; Flament, T.; Le Bourgeois, M.; Chedevergne, F.; Bailly, C.; et al. Predictive factors for lumacaftor/ivacaftor clinical response. J. Cyst. Fibros. 2019, 18, 368–374. [Google Scholar] [CrossRef] [PubMed]
  22. Guerra, L.; D’Oria, S.; Favia, M.; Castellani, S.; Santostasi, T.; Polizzi, A.M.; Mariggio, M.A.; Gallo, C.; Casavola, V.; Montemurro, P.; et al. CFTR-dependent chloride efflux in cystic fibrosis mononuclear cells is increased by ivacaftor therapy. Pediatr. Pulmonol. 2017, 52, 900–908. [Google Scholar] [CrossRef]
  23. Guerra, L.; Favia, M.; Castellani, S.; Barbuti, G.; Montemurro, P.; Diana, A.; Santostasi, T.; Polizzi, A.M.; Mariggio, M.A.; Reshkin, S.J.; et al. Antibiotic therapy affects functional behaviour in cystic fibrosis blood mononuclear cells. Eur. Respir. J. 2015, 46, 558–561. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  24. Sergeev, V.; Chou, F.Y.; Lam, G.Y.; Hamilton, C.M.; Wilcox, P.G.; Quon, B.S. The extrapulmonary effects of cystic fibrosis transmembrane conductance regulator modulators in cystic fibrosis. Ann. Am. Thorac. Soc. 2020, 17, 147–154. [Google Scholar] [CrossRef] [PubMed]
  25. Pohl, K.; Hayes, E.; Keenan, J.; Henry, M.; Meleady, P.; Molloy, K.; Jundi, B.; Bergin, D.A.; McCarthy, C.; McElvaney, O.J.; et al. A neutrophil intrinsic impairment affecting Rab27a and degranulation in cystic fibrosis is corrected by CFTR potentiator therapy. Blood 2014, 124, 999–1009. [Google Scholar] [CrossRef]
  26. Zhang, S.; Shrestha, C.L.; Kopp, B.T. Cystic fibrosis transmembrane conductance regulator (CFTR) modulators have differential effects on cystic fibrosis macrophage function. Sci. Rep. 2018, 8, 17066. [Google Scholar] [CrossRef] [Green Version]
  27. White, M.M.; Geraghty, P.; Hayes, E.; Cox, S.; Leitch, W.; Alfawaz, B.; Lavelle, G.M.; McElvaney, O.J.; Flannery, R.; Keenan, J.; et al. Neutrophil membrane cholesterol content is a key factor in cystic fibrosis lung disease. EBioMedicine 2017, 23, 173–184. [Google Scholar] [CrossRef] [Green Version]
  28. Hisert, K.B.; Schoenfelt, K.Q.; Cooke, G.; Grogan, B.; Launspach, J.L.; Gallagher, C.G.; Donnelly, S.C.; Welsh, M.J.; Singh, P.K.; McKone, E.F.; et al. Ivacaftor-induced proteomic changes suggest monocyte defects may contribute to the pathogenesis of cystic fibrosis. Am. J. Respir. Cell Mol. Biol. 2016, 54, 594–597. [Google Scholar] [CrossRef] [Green Version]
  29. Wainwright, C.E.; Elborn, J.S.; Ramsey, B.W.; Marigowda, G.; Huang, X.; Cipolli, M.; Colombo, C.; Davies, J.C.; De Boeck, K.; Flume, P.A.; et al. Lumacaftor-ivacaftor in patients with cystic fibrosis homozygous for Phe508del CFTR. N. Engl. J. Med. 2015, 373, 220–231. [Google Scholar] [CrossRef] [Green Version]
  30. Kerem, E.; Reisman, J.; Corey, M.; Canny, G.J.; Levison, H. Prediction of mortality in patients with cystic fibrosis. N. Engl. J. Med. 1992, 326, 1187–1191. [Google Scholar] [CrossRef]
  31. Jennings, M.T.; Dezube, R.; Paranjape, S.; West, N.E.; Hong, G.; Braun, A.; Grant, J.; Merlo, C.A.; Lechtzin, N. An observational study of outcomes and tolerances in patients with cystic fibrosis initiated on lumacaftor/ivacaftor. Ann. Am. Thorac. Soc. 2017, 14, 162–1666. [Google Scholar] [CrossRef] [PubMed]
  32. Hubert, D.; Chiron, R.; Camara, B.; Grenet, D.; Prevotat, A.; Bassinet, L.; Dominique, S.; Rault, G.; Macey, J.; Honore, I.; et al. Real-life initiation of lumacaftor/ivacaftor combination in adults with cystic fibrosis homozygous for the Phe508del CFTR mutation and severe lung disease. J. Cyst. Fibros. 2017, 16, 388–391. [Google Scholar] [CrossRef] [PubMed]
  33. Del Porto, P.; Cifani, N.; Guarnieri, S.; Di Domenico, E.G.; Mariggio, M.A.; Spadaro, F.; Guglietta, S.; Anile, M.; Venuta, F.; Quattrucci, S.; et al. Dysfunctional CFTR alters the bactericidal activity of human macrophages against Pseudomonas aeruginosa. PLoS ONE 2011, 6, e19970. [Google Scholar]
  34. Van de Weert-van Leeuwen, P.B.; Van Meegen, M.A.; Speirs, J.J.; Pals, D.J.; Rooijakkers, S.H.; Van der Ent, C.K.; Terheggen-Lagro, S.W.; Arets, H.G.; Beekman, J.M. Optimal complement-mediated phagocytosis of Pseudomonas aeruginosa by monocytes is cystic fibrosis transmembrane conductance regulator-dependent. Am. J. Respir. Cell Mol. Biol. 2013, 49, 463–470. [Google Scholar] [CrossRef] [PubMed]
  35. Bonfield, T.L.; Hodges, C.A.; Cotton, C.U.; Drumm, M.L. Absence of the cystic fibrosis transmembrane regulator (Cftr) from myeloid-derived cells slows resolution of inflammation and infection. J. Leukoc. Biol. 2012, 92, 1111–1122. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  36. Di, A.; Brown, M.E.; Deriy, L.V.; Li, C.; Szeto, F.L.; Chen, Y.; Huang, P.; Tong, J.; Naren, A.P.; Bindokas, V.; et al. CFTR regulates phagosome acidification in macrophages and alters bactericidal activity. Nat. Cell Biol. 2006, 8, 933–944. [Google Scholar] [CrossRef]
Ijms 21 02398 g001 550
Figure 1. Changes in clinical parameters during Orkambi® treatment: (A) sweat chloride levels; (B) FEV1%; (C) BMI; and (D) CRP. Data are shown as mean ± SEM.* p < 0.05.
Figure 1. Changes in clinical parameters during Orkambi® treatment: (A) sweat chloride levels; (B) FEV1%; (C) BMI; and (D) CRP. Data are shown as mean ± SEM.* p < 0.05.
Ijms 21 02398 g001
Ijms 21 02398 g002 550
Figure 2. Changes in marrow-derived peripheral cells during Orkambi® treatment: (A) platelets (n/mm3); (B) total WBC (n/mm3); (C) neutrophils (% of WBC); (D) eosinophils (% of WBC); (E) basophils (% of WBC); (F) monocytes (% of WBC); and (G) lymphocytes (% of WBC). Data are shown as mean ± SEM.
Figure 2. Changes in marrow-derived peripheral cells during Orkambi® treatment: (A) platelets (n/mm3); (B) total WBC (n/mm3); (C) neutrophils (% of WBC); (D) eosinophils (% of WBC); (E) basophils (% of WBC); (F) monocytes (% of WBC); and (G) lymphocytes (% of WBC). Data are shown as mean ± SEM.
Ijms 21 02398 g002
Ijms 21 02398 g003 550
Figure 3. CFTR activity and protein in MNCs: (A) cumulative data of CFTR activity obtained from 14 patients; (B) a representative Western blot of CFTR protein; and (C) densitometric analysis of Western blots represented as the OD ratio of Band C over Bands B and C in three CF subjects and in a pool derived from five non-CF subjects. Data are shown as mean ± SEM. * p < 0.05, ** p < 0.01, *** p < 0.001.
Figure 3. CFTR activity and protein in MNCs: (A) cumulative data of CFTR activity obtained from 14 patients; (B) a representative Western blot of CFTR protein; and (C) densitometric analysis of Western blots represented as the OD ratio of Band C over Bands B and C in three CF subjects and in a pool derived from five non-CF subjects. Data are shown as mean ± SEM. * p < 0.05, ** p < 0.01, *** p < 0.001.
Ijms 21 02398 g003
Ijms 21 02398 g004 550
Figure 4. Correlations and cluster analysis over all time points during Orkambi treatment: (A) correlation graph; and (B) cluster analysis.
Figure 4. Correlations and cluster analysis over all time points during Orkambi treatment: (A) correlation graph; and (B) cluster analysis.
Ijms 21 02398 g004
Table
Table 1. Clinical characteristics of enrolled patients (n = 14) before Orkambi® treatment.
Table 1. Clinical characteristics of enrolled patients (n = 14) before Orkambi® treatment.
Min. ValueMedianMax. Value25th Percentile75th Percentile
Sweat chloride (mEq/L)97.0123.5139.0116.5132.0
FEV1%21.551.4101.639.088.3
BMI (kg/m2)16.720.623.918.521.8
CRP (mg/dL)2.93.918.52.913.5

Share and Cite

MDPI and ACS Style

Favia, M.; Gallo, C.; Guerra, L.; De Venuto, D.; Diana, A.; Polizzi, A.M.; Montemurro, P.; Mariggiò, M.A.; Leonetti, G.; Manca, A.; et al. Treatment of Cystic Fibrosis Patients Homozygous for F508del with Lumacaftor-Ivacaftor (Orkambi®) Restores Defective CFTR Channel Function in Circulating Mononuclear Cells. Int. J. Mol. Sci. 2020, 21, 2398. https://0-doi-org.brum.beds.ac.uk/10.3390/ijms21072398

AMA Style

Favia M, Gallo C, Guerra L, De Venuto D, Diana A, Polizzi AM, Montemurro P, Mariggiò MA, Leonetti G, Manca A, et al. Treatment of Cystic Fibrosis Patients Homozygous for F508del with Lumacaftor-Ivacaftor (Orkambi®) Restores Defective CFTR Channel Function in Circulating Mononuclear Cells. International Journal of Molecular Sciences. 2020; 21(7):2398. https://0-doi-org.brum.beds.ac.uk/10.3390/ijms21072398

Chicago/Turabian Style

Favia, Maria, Crescenzio Gallo, Lorenzo Guerra, Domenica De Venuto, Anna Diana, Angela Maria Polizzi, Pasqualina Montemurro, Maria Addolorata Mariggiò, Giuseppina Leonetti, Antonio Manca, and et al. 2020. "Treatment of Cystic Fibrosis Patients Homozygous for F508del with Lumacaftor-Ivacaftor (Orkambi®) Restores Defective CFTR Channel Function in Circulating Mononuclear Cells" International Journal of Molecular Sciences 21, no. 7: 2398. https://0-doi-org.brum.beds.ac.uk/10.3390/ijms21072398

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop