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Clinical studies with modulators of the Cystic Fibrosis Transmembrane conductance Regulator (CFTR) protein have demonstrated that functional restoration of the mutated CFTR can lead to substantial clinical benefit. However, studies have shown highly variable patient responses. The objective of this study was to determine a biomarker predictive of the clinical response. CFTR function was assessed in vivo via nasal potential difference (NPD) and in human nasal epithelial (HNE) cultures by the response to Forskolin/IBMX and the CFTR potentiator VX-770 in short-circuit-current (IscF/I+V) experiments. CFTR expression was evaluated by apical membrane fluorescence semi-quantification. Isc measurements discriminated CFTR function between controls, healthy heterozygotes, patients homozygous for the severe F508del mutation and patients with genotypes leading to absent or residual function. IscF/I+V correlated with CFTR cellular apical expression and NPD measurements. The CFTR correctors lumacaftor and tezacaftor significantly increased the IscF/I+V response to about 25% (SEM=4.4) of the WT-CFTR level and the CFTR apical expression to about 22% (SEM=4.6) of the WT-CFTR level in F508del/F508del HNE cells. The level of CFTR correction in HNE cultures significantly correlated with the FEV1 change at 6 months in 8 patients treated with CFTR modulators. We provide the first evidence that correction of CFTR function in HNE cell cultures can predict respiratory improvement by CFTR modulators.
Cystic Fibrosis (CF) is the most frequent lethal autosomic disease in the Caucasian population. In its typical form it induces the production of a highly salted sweat, pancreatic insufficiency and a progressive destructive infected bronchopathy which leads to respiratory failure1. CF is caused by mutations in the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) gene coding for the CFTR protein, a member of the ATP-binding cassette transporter family of membrane proteins. It forms a small-conductance, chloride (Cl−) channel that is gated by protein kinase A-mediated phosphorylation, and ATP binding/ hydrolysis2.
The most frequent mutation, the deletion of one amino-acid phenylalanine at position 508, is associated with misfolding of the protein leading to its degradation by the proteasomal pathway. Corrector therapy aims to stabilize the folding of the protein and limit its degradation. As a result, little to no F508del-CFTR is delivered to the cell surface, and CFTR Cl− transport activity is abolished2. Other mutations limit the gating of the channel, such as the G551D mutation, and their function is restored by therapies potentiating the opening of the channel.
A recent proof-of-concept study on the CFTR potentiator ivacaftor (VX-770)3 has demonstrated that pharmacological manipulation of the G551D-CFTR protein can translate into clinical benefit for CF patients and potentially profoundly modify the disease prognosis4, 5. This has also been demonstrated for other malfunctioning proteins affecting the gating of the channel6. Improvement of the in vitro activity of F508del-CFTR requires the combination of lumacaftor (VX-809)-CFTR corrector7 and ivacaftor CFTR potentiator3. However, such therapy is associated with variable clinical responsiveness. This was illustrated in a therapeutic trial testing the lumacaftor and ivacaftor combination (Orkambi) in F508del homozygous patients8. Indeed, only 25% of the subjects showed respiratory function improvement greater than 10% after 6 months of treatment, suggesting that the efficacy of CFTR modulators may differ according to the patient8. Different hypothesis have been proposed to explain the variable efficacy of Orkambi therapy, including destabilization of lumacaftor rescued F508del-CFTR by chronic ivacaftor treatment9, 10, the rescue of a subpopulation of F508del-CFTR Cl− channels11, and action of Orkambi on other factors than transepithelial ion transport such as mucociliary clearance12. These observations highlight the importance of finding biomarkers that can predict the individual patients’ responses.
As the main goal of CFTR modulator therapy is to retard the disease progression in patients’ lungs, scientists have focused on respiratory epithelial cells. Human bronchial epithelial (HBE) cells have been used to assess the efficacy of CFTR modulators in vitro 3, 7, 9, 10, 13–16. However, these cells cannot be used routinely, as they are derived from explanted lungs. To overcome this problem, human nasal epithelial (HNE) cell cultures have been developed. These are easy to collect by simple nasal brushing and allow quantification of cyclic AMP (cAMP)-mediated Cl− transport as a surrogate marker of CFTR function.
Although pioneering studies have shown that primary HNE cells recapitulate properties of lower airway epithelial cells17–19, there are no data showing their ability to distinguish levels of CFTR function according to CF genotype. Moreover, the correlation between CFTR bioactivity assessed in vitro in this model and in vivo in the nasal mucosa of the same patients has never been investigated. Furthermore, no systematic study has assessed the variability of HNE cell responses to CFTR correctors. Finally, and most importantly, whether the rescue of CFTR activity with CFTR modulators in this model is predictive of the clinical efficacy in patients, needs to be determined.
In this study, we first characterized CFTR expression and function in HNE cells isolated from CF patients, healthy controls, and heterozygotes to correlate in vitro functional data with in vivo nasal potential difference measurement elicited by cAMP agonists. We then undertook a systematic study to evaluate the correction of CFTR function by two CFTR correctors, lumacaftor and tezacaftor (VX-661), in HNE cultures issued from patients homozygous for the F508del mutation or carrying CFTR genotypes displaying a wide spectrum of CFTR activity. Finally, we assessed the predictive value of the primary HNE cell cultures by comparing the pharmacological rescue of CF mutations by CFTR modulators in vitro with the clinical efficacy of these agents in CF patients.
We characterized the properties of non-expanded cultures at passage 0 to remain as close as possible to the in vivo physiology. Both primary HNE and HBE cells displayed typical features of polarized and differentiated respiratory epithelium (Supplementary Fig. S1a,b). The ciliated cells were the predominant type of cells, accounting for 47–91% of all types of cells in HNE cultures, as assessed by the percentage of cells with alpha-tubulin staining (Supplementary Fig. S1a,b).
Short-circuit-current (Isc) experiments showed statistically significant differences between wt/wt and F508del/F508del HNE cultures for Isc changes induced by Forskolin/IBMX+VX-770 and CFTRinh172, similarly to HBE cell cultures (Fig. 1a,b; Supplementary Fig. S1c; Table 1). The only difference between HNE and HBE cell cultures, although not statistically significant, was the mean basal current, which was associated with an increased response to Amiloride (IscAmiloride) in wt/wt HBE versus HNE cells (Fig. 1a,b; Table 1). The wt/F508del HNE cells presented basal currents (19.4±6.2µA/cm2) and IscAmiloride (−8.8±4.7µA/cm2) that were not statistically different from the responses observed in wt/wt cells. In contrast, the responses to Forskolin/IBMX+VX-770 (IscF/I+V 5.1±1.4µA/cm2) and CFTRinh172 (IscCFTRinh172−9.2 ±2.4µA/cm2) were significantly different from both the wt/wt and F508del homozygous HNE cells (Fig. 1b). The variation of Isc after Forskolin/IBMX+VX-770, which is the main endpoint for corrector efficacy assessment, was analyzed to gain further insight into inter- and intra-subject variability. Both in wt/wt and F508del homozygous cell cultures, the inter-subject variability accounted for around 2/3 of the total variability with 67% of total variance for wt/wt cells (inter-subject variability 0.47 and intra-subject variability 0.23; Intra-Class Correlation ICC=0.47/(0.47+0.23)=0.67), and 70% for F508del/F508del cells (inter-subject variability 0.6 and intra-subject variability 0.23; ICC=0.6/(0.6+0.23)=0.7), as estimated with linear random effect model, with no significant difference between HNE and HBE cells.
There was no significant difference for the CFTR staining patterns between HNE and HBE cells (Fig. 1c,d). Apical CFTR staining was observed in 86% (83–91%) of wt/wt HNE and HBE cells, whereas it was present in only 8% (3–18%) of F508del cells. The average corrected apical fluorescence was around 5-fold weaker in F508del homozygous cells than in wt/wt cells (Table 1). The CFTR staining was intermediate in wt/CF HNE cells with 57% (49–67%) of positive cells, but the average corrected apical fluorescence was close to normal (Fig. 1d). The proportion of cells with apical immunostaining was significantly correlated with the average corrected apical fluorescence (Supplementary Fig. S2 ).
To gain further insight into the characterization of the HNE model, we compared the IscF/I+V changes in cell cultures from patients with genotypes associated with a wide range of functional defects to the mean IscF/I+V value in wt/wt cells.
As expected, the genotypes including premature termination codon (PTC) (Y122X, G542X), deletion generating PTC (394delTT), severe splicing mutations (711+1G>T, 1717 1G>A), and the misfolding N1303K mutation, did not display CFTR-dependent Cl− transport, whereas the terminally truncated mutation (E1418X), the mild splicing mutation (2789+5G>A), and mutations associated with atypical CF such as D1152H, displayed residual function (Fig. 2, x-axis). Finally, two genotypes involving mutations of uncertain liability L997F/R258G20 and G1244E/R352Q21 (Supplementary Fig. S7) displayed WT level activity. This gradient in residual Cl− transport was significantly correlated to apical CFTR staining (Fig. 2, y-axis; Supplementary Fig. S2).
To elucidate the physiological relevance of the HNE cell culture model, we compared IscF/I+V to the response to low-Cl− solution and Isoproterenol, as assessed by nasal potential difference (NPD) in the same patient (Fig. 3, Supplementary Figs S5, S6 and S7). The correlation was high (R 2=0.82, p<0.0001), indicating that the primary HNE reproduce the in vivo detected differences in the mutant CFTR activity.
In contrast to Cl−, the Na+ transport, evaluated by the response to Amiloride during NPD and Isc, did not display such variation (R 2=0.04, NS; simple regression analysis), and it was not correlated to IscF/I+V values (R 2=0.0004, NS; simple regression analysis).
The effect of lumacaftor was evaluated in conditionally reprogrammed HNE (CR-HNE) cultures from 11 F508del homozygous patients and in HBE cultures from 11 F508del homozygous patients. To increase the number of filters available, we used conditionally reprogrammed and re-differentiated HNE cells but remained at passage 1 to maintain comparable CFTR expression to that observed in non-amplified cells. Both in patients homozygous for F508del and wt/wt subjects, the magnitude of Isc changes to Amiloride, Forskolin/IBMX+VX-770 and CFTRinh172 in CR-HNE were not significantly different from those obtained in primary non-expanded HNE cells (e.g. IscF/I+V=0.8µA/cm2 (range min-max 1.46) in non-treated F508del/F508del CR-HNE n=15; and 0.2µA/cm2 (range min-max 0.58) in non-treated non-reprogrammed HNE n=12).
Lumacaftor treatment significantly increased the average IscF/I+V in HNE and HBE cells as compared to DMSO by a mean of 1.8µA/cm2 (SEM=0.5). This was evaluated in 22 different patients (in 44 DMSO treated and 44 lumacaftor treated inserts). This correction allowed to reach an average of 25% (SEM=4.4) of the WT-CFTR level (p<10−6) (Fig. 4a). Lumacaftor was able to correct CFTR activity above 10% of the WT-CFTR, a level observed in patients with mild disease22–24, for 16 patients out of the 22 tested, and above the mean level obtained in healthy heterozygotes for 4 patients.
The variability of the treatment effect was mainly due to inter-patient variability (0.87) rather than intra-patient variability (0.25), which accounted for 77% of the total variability (intra-class correlation coefficient ratio of inter-patient variability over inter+intra-patient variability), as estimated with linear random effect model. However, the lumacaftor-induced change was not significantly different in HBE versus HNE cultures. The inter-patient variability was not associated with increased local nasal inflammation, as assessed by local visualization before nasal cell sampling, nor patients’ sputum colonization. The quantification of the VX-809 correction variability enabled us to calculate the number of filters necessary to assess the effect of CFTR corrector in F508del/F508del patients with a reliable power (Supplementary Table 1).
Tezacaftor was evaluated in HNE and HBE cultures of 14 F508del homozygous patients. It induced a significant increase of IscF/I+V by a mean of 2.5µA/cm2 up to 27.4% of the WT-CFTR (SEM=3.8; p=0.001) (Supplementary Fig. S3a). A correction of the Cl− secretion above 10% of the WT average, was obtained in 13 out of 14 patients, and over the healthy heterozygote range in 2 patients.
The Forskolin/IBMX+VX-770-mediated response was not modified in genotypes with absent basal CFTR function associating F508del-CFTR with PTC mutations, 711+1G>T or N1303K (Fig. 4b). In contrast, the F508del/1717-1G>A and F508del/394delTT genotypes were strongly corrected, respectively by 11.2% and 29.6% of the average WT-CFTR level. Interestingly, the genotypes with strong initial residual Cl− secretion, such as F508del/D1152H and L997F/R258G, displayed considerable correction, (respectively 40% and 74.6% from the basal value) reaching the WT value. This is significantly different from that observed in the F508del homozygote HNEs (18%).
Pooling the Isc data from all the genotypes showed that the level of correction by lumacaftor was significantly correlated with the presence of residual basal CFTR-dependent Cl− secretion (Fig. 5a). This was significantly correlated with the increase of CFTR expression at the apical face of the epithelium, as illustrated in Fig. 5b (and Supplementary Fig. S2). To investigate whether this could be related to culture dependent variation, we assessed the proportion of ciliated cells, the transepithelial resistance (RT) and the height of the epithelial layer. We did not find any difference for those parameters between the DMSO and the lumacaftor treated filters, nor between the “responder” (i.e. above 10% of the WT average Cl− secretion) and the “non-responder” samples. This was further assessed by the absence of significant correlation between ΔIscF/I+V and either RT (R 2=0.0005, NS) or proportion of ciliated cells (R 2=0.38, NS). This suggests that the correction effect was not due to differences in cell differentiation.
The average correction of IscF/I+V was not significantly different between lumacaftor and tezacaftor, both for F508del homozygous genotypes, however, on an individual basis, the effect of the two molecules may be different (NS, paired signed rank comparison) (Supplementary Fig. S3b).
We finally evaluated lumacaftor on healthy wt/F508del heterozygous HNE cells from 5 donors. The average increase of ΔIscF/I+V upon lumacaftor treatment was 23% (SEM=16) of the average WT-CFTR level. Moreover, like in CF F508del/N1303K cells, the HNE with wt/N1303K genotype did not respond to lumacaftor treatment (Fig. 4b).
CFTR function correction in HNE cultures was compared to its clinical efficacy, as assessed by the drug induced change of FEV1 at 6 months in 7 F508del homozygous patients treated with Orkambi and F508del/S549N patient treated with ivacaftor (Kalydeco) (Fig. 6).
Patients 1, 2 and 3 were considered non-responders due to decreased FEV1 by 7% or no change of FEV1, respectively, after 6 months of treatment (Fig. 6). Patient 4 showed moderate 5% improvement of FEV1 at 6 months of Orkambi treatment. Patients 5, 6 and 7 were considered responders because their respiratory function increased by more than 10% (Fig. 6).
CFTR activity correction upon Orkambi treatment in HNE cell cultures, as assessed by the drug induced change of the response to Forskolin/IBMX+VX-770, correlated significantly with the FEV1 change induced by drug (R 2=0.95, p<0.0001) (Fig. 6 ). IscF/I+V did not vary in HNE cells from Patients 1, 2, and 3 who did not improve clinically. The highest improvement in Cl− secretion was measured in Patients 6 and 7, with IscF/I+V values reaching 33% and 61%, respectively, of the average WT-CFTR function. This was correlated with the increase in apical CFTR expression (Fig. 5b). All patients who exhibited correction of their respiratory function above 5% displayed a mean change of IscF/I+V, expressed as the percentage of the average WT level, above 10%.
The case report of Patient 8, carrying the F508del/S549N genotype (Fig. 6), illustrates these observations. The patient underwent a life-threatening exacerbation after hemoptysis, justifying lung transplant indication. Treatment with ivacaftor resulted in acute, impressive improvement in respiratory function, which avoided lung transplantation and greatly increased quality of life (Supplementary Fig. S4a,b). In vitro evaluation demonstrated no significant increase in the immunostaining of apical CFTR upon ivacaftor (Fig. 5b) but a strong effect of ivacaftor on IscF/I+V, reaching 60% (correction by 38%) of average WT-CFTR function (Supplementary Fig. S4c).
Our study demonstrates that primary HNE cell cultures recapitulate the properties of primary HBE cultures from both CF and non-CF individuals.
To obtain the target level of correction, we first focused on HNE cells from healthy controls and on F508del homozygous patients, as this is the most frequent mutation. We did not find any marked differences between HBE and HNE cells in terms of cell differentiation, electrical resistance, and CFTR function/expression, as already reported by McDougall et al.19 and Devalia et al.25. The increased Na+ transport of wt/wt HBE versus HNE cells, probably reflects the increase in the ENaC relative expression changes from the proximal to distal regions of the human respiratory tracts26. We also verified that there was no significant change in CFTR bioactivity after expansion of HNE at the first passage, as also recently reported by Gentzsch et al.27, and supported by transcriptomic data that did not evidence any changes in CFTR expression28.
Our study is the first to focus on the range of CFTR function and expression in F508del homozygous HNE cells. We demonstrated that the variability in the cAMP-dependent Cl− transport was mainly due to inter-subject variability. We aimed to limit the intrinsic variability of experimentation from human sampling. To avoid this we standardized as much as possible the experiments by evaluating cells at the same passage 1, eliciting cultures with the same level of trans-epithelial resistance. This was also the reason why we decided to use first the non-reprogrammed cells. Indeed this strategy might have displayed an additional level of variability, linked to differences in the seeding composition of progenitors, as recently speculated28.
Resampling different subjects (1 healthy control, 1 F508del homozygous subject, and 1 F508del/E1418X subject) confirmed that the Forskolin/IBMX+VX-770 responses variability was limited. Moreover, values for RT, inhibition of Amiloride-sensitive Na+ currents, and activation of cAMP-dependent Cl− currents were in the range of already published values for primary HNE cultures17, 29–33 sampled from healthy donors (RT ranging from 427±31 to 964±545 Ωcm2 17, 29, 33; IscAmiloride ranging from 23.9±8.5 to 28±3µA/cm2 17, 33; IscF/I+V ranging from 7±2 to 16.1±3.8µA/cm2 17, 31, 33) and F508del homozygous patients (RT ranging from 542±65 to 633±256 Ωcm2 17, 33; IscAmiloride ranging from 35 to 61±8µA/cm2 31, 33; IscF/I+V ranging from 0.1±0.1 to 0.7±0.2µA/cm2 17, 31, 33. Furthermore, the response to Forskolin/IBMX+VX-770, display a relatively low variability both in healthy subjects (mean: 11.6µA/cm2; SEM: 1.7) and F508del homozygotes (mean: 0.2µA/cm2; SEM: 0.09). The fact that this response was able to differentiate genotypes with residual CFTR function supports the conclusion that the experimental variability is indeed mainly due to inter-individual and not inter-experimental variation.
The Isc response to Forskolin/IBMX+VX-770, which allowed quantification of the CFTR-mediated Cl− secretion measurements, was accurate enough to detect different levels of CFTR between controls, healthy heterozygotes, and patients with genotypes displaying from absent to residual CFTR function. We showed for the first time that the level of CFTR activity in vitro correlated with in vivo CFTR activity, as measured by NPD. Finally, and most importantly, this CFTR functional spectrum was related to a gradient in CFTR expression at the apical membrane. Altogether, these findings represent strong support for the physiological relevance of the evaluation of CFTR-mediated Cl− transport in HNE cell cultures.
We assessed CFTR correction by lumacaftor and tezacaftor in a large set of F508del homozygous HNE cell cultures and evidenced a substantial variability. This observation cannot be related to the number of passages – all the HNE were assessed at passage 1- nor to the differentiation pattern as the transepithelial resistance, the height of the epithelial layer and the proportion of ciliated cells were similar among the “responder” and the “non-responder” samples. Interestingly, the level of correction correlated to the basal level of CFTR activity suggesting that other causes may be considered, such as associations of F508del with other mutations or CFTR polymorphisms which may affect CFTR folding or post-transcriptional modification modulating CFTR biogenesis34.
Interestingly, compound F508del heterozygotes genotypes displayed a significant correction after lumacaftor or tezacaftor treatment. This was unexpectedly the case for deletion and severe splicing mutations35, but also observed for mutation associated with atypical CF (D1152H)36. This broadens the population of patients that could benefit from lumacaftor or tezacaftor.
Most importantly, our study is the first to provide evidence that quantification of the CFTR-mediated Cl− secretion in patient-derived HNE cells may be a valuable surrogate biomarker to predict the clinical response. Indeed, we found that only patients whose HNE cells displayed an increase in IscF/I+V above 10% of the WT level, exhibited significant clinical improvement at 6 months. The threshold of 10% was considered clinically relevant, as it is associated with a mild disease correlated to higher rates of pancreatic sufficiency, less elevated sweat chloride levels and milder respiratory manifestations22, 24. Conversely, the patients whose cells did not display any significant correction did not improve clinically.
Such data are particularly relevant in the context of emergent therapies that rescue CFTR to identify subjects with CF who may benefit from CFTR-modulating drugs. This has been already shown in organoid cultures derived from the rectal epithelia. Indeed, Dekkers et al., showed that the Forskolin induced swelling response correlated to some extent to the expected level of CFTR activity37. CFTR function and responses to ivacaftor and lumacaftor was studied in subjects with CF, who expressed a broad range of CFTR mutations. In vitro drug responses in rectal organoids positively correlated with published outcome data from clinical trials with lumacaftor and ivacaftor. Importantly, selecting two subjects expressing an uncharacterized rare CFTR genotype the authors showed a correlation between the clinical responses to treatment with ivacaftor and in vitro measurements of CFTR function in patient-derived rectal organoids. However, it must be pointed out that the proteomic and transcriptomic background in intestine is different from that of the respiratory epithelium. As the target tissue of the therapy is the lung, it is mandatory to derive also a surrogate marker for clinical efficacy from the respiratory epithelium.
Indeed, implementation of a preclinical biomarker, such as the quantification of CFTR-mediated Cl− secretion in patient-derived HNE cells might allow the right drug to be targeted for the right patient. This will also allow detection of patients with other genotypes than F508del that are responsive to corrector therapies. This new classification, based on “theratype” and not only genotype34, is driven by patient-specific responses, thereby providing a rationale for a personalized medicine strategy tailored for every CF patient.
Our study provides evidence that the functional restoration of CFTR in HNE cell cultures is appropriate to predict the clinical benefit from a CFTR modulator. This individualized medicine strategy would allow “good” responders for a specific drug to be targeted and treated, thereby providing the drug only to patients predicted to benefit from and repurpose the non-responders to clinical trials with other compounds. This constitutes the basis for a future personalized therapy strategy for CF, which will have a huge influence in bringing medicines to all patients. This heralds a new era in CF care where therapy will address the basic defect of the disease.
CF patients, healthy heterozygous subjects, and healthy non-CF carriers were recruited for HNE sampling (Clinical Trials: NCT02965326). The exclusion criteria were smoking, local nasal treatment and rhinitis at the time of sampling. The study was approved by the Ile de France 2 Ethics Committee, and written, informed consent was obtained from each adult and parent. (AFSSAPS (ANSM) B1005423-40, n° Eudract 2010-A00392-37; CPP IDF2: 2010-05-03-3). All experiments were performed in accordance with the guidelines and regulations described by the Declaration of Helsinki and the low Huriet-Serusclat on human research ethics. HBE cells were derived from lung explants after written informed consent from CF and non-CF subjects. In a second part of study, patients treated with Orkambi or Kalydeco were evaluated for respiratory improvement after at least 6 months of treatment. In this subgroup, nasal cells were always sampled before starting the modulator treatment.
HNE cells were sampled by nasal brushing of both nostrils after local visualization of the nasal mucosa. HBE cells were isolated from bronchial explants as previously described38. Freshly isolated HBE or HNE cells were then seeded on porous filters (0.33cm2, Transwell, Corning) and supplemented with culture medium. After 2 days, cells were cultured in an air-liquid interface for 3–4 weeks. At least 2 filters were analyzed per patient to assess reliable results.
To increase the number of filters available to test the corrector efficacy, we used conditionally reprogrammed and re-differentiated HNE cells39. CFTR modulators, VX-809 lumacaftor (3µM) and VX-661 tezacaftor (3µM) dissolved in DMSO, were added to the basal side of polarized HNE or HBE cells grown at an air-liquid interface and incubated during 2 days in 5% CO2 at 37°C, before experimentation. To evaluate the HNE cells of patients treated with Orkambi we also tested the association of lumacaftor with ivacaftor (100nM) for 48h. Patient’s cells treated with DMSO constituted their own control. The supplementary information provides further details about this method.
The short-circuit-current (Isc) was measured under voltage clamp conditions with an EVC4000 Precision V/I Clamp (World Precision Instruments). For all measurements chloride concentration gradient across the epithelium was applied by differential composition of basal and apical Ringer solutions. The basal Ringer solution contained: 145mM NaCl, 3.3mM K2HPO4, 10mM HEPES, 10mM D-Glucose, 1.2mM MgCl2, and 1.2mM CaCl2 and apical solution contained: 145mM Na-Gluconate, 3.3mM K2HPO4, 10mM HEPES, 10mM D-Glucose, 1.2mM MgCl2, 1.2mM CaCl2. Inhibitors and activators were added after stabilization of baseline Isc:sodium (Na+)-channel blocker Amiloride (100µM) to inhibit apical epithelial Na+ channel (ENaC); cAMP agonists Forskolin (10µM) and 3-isobutyl-1-methylxanthine (IBMX 100µM) to activate the transepithelial cAMP-dependent current (including Cl− transport through CFTR channels); VX-770 (10µM) to potentiate CFTR activity; CFTR inhibitor CFTRinh172 (5µM) to specifically inhibit CFTR; and ATP (100µM) to challenge the purinergic calcium-dependent Cl− secretion. The sum of the change after Forskolin/IBMX and VX-770 (IscF/I+V) served as an index of CFTR function. The supplementary information provides further details about this method.
CFTR immuno-detection was performed as previously described40. Apical CFTR staining was assessed semi quantitatively as the percentage of cells displaying apical staining multiplied by the average corrected apical fluorescence41. The supplementary information provides further details about these methods.
NPD measurement was performed as described previously42. The sum of low chloride and Isoproterenol (LowCl–Iso) served as an index of CFTR function. The supplementary information provides further details about this method.
Statistical analysis was performed using S.A.S software. As several HNE/HBE filters were obtained from a single patient, quantitative parameters were expressed as median values per patient. Means (±SEM) were calculated from the median values per patient. Comparisons between groups were carried out using the Mann-Whitney U test. Correlation coefficients were calculated by Spearman’s rank correlation. R 2 coefficients were calculated to assess how the data fitted to the regression model.
As the number of cultures tested for each patient varied, a linear random-effects model was used to decompose inter- and intra-patient variability. The part of inter-patient variability was expressed by the intra-class correlation coefficient defined as the ratio of inter over inter+intra variability estimates. Lumacaftor efficacy in the F508del/F508del patients was evaluated with the mixed effect linear model, using treatment as the fixed effect and the patient as the random effect to consider the inter-patient and inter-filter variability. All statistical tests were two-sided and a p-value<0.05 was considered statistically significant.
We acknowledge Prof. Gergely L. Lukacs for advices on the manuscript, Christelle Moquereau for participation in the experimental part of the study, André Coste for demonstrating the nasal brushing procedure and Estelle Escudier for demonstrating the primary cell culture protocol. Microscopy images were acquired at the Cell Imaging Platform of the Necker Institute. We are very grateful to Dr F. Chedeverne, Dr M Le Bourgeois, Dr C Bailly, Dr Flament and D Achimostos for referring patients. We thank very warmly all patients and their families for participation in the study. Supported by Vaincre La Mucoviscidose, Grant RC20160501612; and ABCF Association, Grant ABCF-1-2016.
I.M.P.: acquisition, analysis and interpretation of the data, manuscript preparation; A.H.: acquisition and analysis of the data; J.S.: acquisition and analysis of the data; J.P.J.: analysis and interpretation of the data; F.P.B.: provision of bronchial explants; A.C.: provision of bronchial explants, interpretation of the data; P.B.: provision of bronchial explants; M.F.: provision of bronchial explants; N.S.B.: provision of bronchial explants, interpretation of the data; D.G.: provision of bronchial explants; M.T.: provision of bronchial explants; J.M.: provision of bronchial explants; V.U.: interpretation of the data, revision of the manuscript; M.M.: acquisition, analysis and interpretation of the data; E.G.B.: interpretation of the data, manuscript revision; A.H.: interpretation of the data, revision of the manuscript; A.E.: interpretation of the data, revision of the work and the manuscript; I.S.G.: conception and design of the work, interpretation of the data, manuscript preparation, revision of the work, final approval.
The authors declare that they have no competing interests.
Electronic supplementary material
Supplementary information accompanies this paper at doi:10.1038/s41598-017-07504-1