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01.12.2015 | Research article | Ausgabe 1/2015 Open Access

BMC Pulmonary Medicine 1/2015

Safety and performance analysis of acriflavine and methylene blue for in vivo imaging of precancerous lesions using fibered confocal fluorescence microscopy (FCFM): an experimental study

BMC Pulmonary Medicine > Ausgabe 1/2015
Bérengère Obstoy, Mathieu Salaun, Liana Veresezan, Richard Sesboüé, Pierre Bohn, François-Xavier Boland, Luc Thiberville
Wichtige Hinweise

Competing interests

LT received a grant research from Mauna Kea Technologies (€1000); was invited as speaker at the International Conference on Cellvzio® Users in 2010 and 2011 (no fee) by Mauna Kea Technologies; and travel to the ACCP congress was funded by Mauna Kea Technologies in 2007. LT is listed as co-author on a patent related to pCLE, shared between Rouen University and Mauna Kea Technologies.
MS was invited to attend the International Conference on Cellvizio® Users by Mauna Kea Technologies in 2011; has been member of a Medical Advisory Board for Mauna Kea Tech. (€750). None of the authors has a financial relationship with a commercial entity that has an interest with the subject of this manuscript.

Authors’ contributions

The authors contributed to this work as follows: BO, LT, and MS carried out the conception and design of the study, the acquisition, analysis and interpretation of the microimaging data as well as drafted the manuscript. BO and RS carried out the genotoxicity assessment. BO and LV participated in the histological process and assessment of the cheek pouch lesions. BO and PB participated in the animal and cellular experiments, and in drafting the manuscript. F-XB participated in setting up the animal model. All authors read and approved the final manuscript.
Fibered Confocal Fluorescence Microscopy
Laser Scanning Unit
Methylene blue
probe-based Confocal Laser Endomicroscopy


Fibered confocal fluorescence microscopy (FCFM) or probe-based Confocal Endomicroscopy (pCLE) is a recent in vivo optical imaging technique that is based on the principle of confocal microscopy. In this technique, the microscope’s objective is replaced by a flexible miniprobe containing 30 000 optical fibers. The probe can be inserted into the working channel of an endoscope and pushed beyond the endoscopic view so as to analyze the distal lung microstructures that come in contact with the tip of the probe. When used in the respiratory tract, this minimally invasive endoscopic technique enables the fluorescence imaging of both proximal bronchi and distal pulmonary interstitial microstructures in humans [ 1, 2].
In humans, elastin is the main constituent of interstitial lung tissue. Elastin excitation at 488 nm wave-length light produces autofluorescence that can be captured by FCFM, and allows the sub-epithelial layer of the bronchial mucosa to be visualized [ 3]. In a previous study, we demonstrated that the technique makes it possible to analyze the microstructure of the bronchial basement membrane but not the bronchial epithelial cell layer [ 3]. Consequently, exogenous cellular fluorophores must be employed to observe simultaneously both the epithelial and sub-epithelial layers of the bronchial mucosa using FCFM [ 4, 5].
FCFM studies of the bronchial mucosa have recently been carried out at 488 nm excitation, using either acriflavine, an intercalating DNA element that allows cell nuclei to be imaged [ 1], or fluorescein, a fluorophore that does not penetrate cells but allows cell interfaces to be visualized [ 6]. When using a FCFM system at 660 nm, as there is no autofluorescence at 660 nm in the respiratory tract, methylene blue, a fluorophore that temporarily binds to nuclear and mitochondrial DNA, can be used, thus allowing for nuclear and cytoplasmic imaging [ 4, 7].
The majority of epithelial cancers involving the proximal respiratory system, such as squamous cell carcinomas, are believed to be preceded by precancerous lesions [ 8]. This multi-step carcinogenesis involves different stages, such as hyperplastic lesions, mild/moderate/severe dysplastic lesions, and in situ carcinomas. Previous studies have shown that preneoplastic bronchial lesions exhibit a 2-year progression rate of 5% for low-grade dysplasias, 30% for high-grade dysplasias, and 80% for in situ carcinomas [ 9].
The in vivo diagnosis of these small-size lesions is currently based on autofluorescence bronchoscopy with targeted biopsies of the areas that display less fluorescence. The main drawback of this endoscopic technique, which is now well-documented, is its low specificity, which is caused by bronchial fluorescence alterations that occur during mucosal inflammation or non-neoplastic hyper-vascularization [ 10].
We hypothesized that FCFM along with the topical use of fluorophores such as methylene blue or acriflavine would allow the microscopic imaging and diagnosis of the different preneoplastic stages of the respiratory tract lesions, in vivo, in situ.
The objectives of this study were:
first, to test whether FCFM with methylene blue or acriflavine allows for diagnosing in vivo the different stages of squamous carcinoma development in the experimental cheek pouch model; second, to test the genotoxicity of methylene blue and acriflavine during FCFM.”



Six weeks-old, 100 g, Syrian golden hamsters (Janvier®, France), were housed in groups of three in pre-sterilized cages placed in a positive/negative ventilation housing system (PNCT3HR30EZ model, Allentown Inc., Allentown, New Jersey, USA). The ambient temperature was 22°C. The circadian rhythm was maintained. The animals had unlimited access to food and water. The study started following 5 days of acclimatization. The animal experiment complied with ethics rules of the Rouen University, and the study protocol was approved by the regional committee for animal ethics (the Normandy ethic committee for experimentation on animals, CENOMEXA; N/03-12-10/25/12).
Malignant transformation of the hamster’s right cheek pouch was obtained by suturing an implant impregnated with dimethylbenzanthracene (DMBA) (Sigma Aldrich, St. Louis, USA) according to the technique described by Heller et al. [ 11]. Figure  1A shows the implant sutured into the jugal mucosa.
The DMBA implant was sutured under general anesthesia using an intra-peritoneal injection of a mixture of ketamine 30 mg/kg (Merial, Lyon, France) and xylazine 10 mg/kg (Bayer, Leverkusen, Germany) following gaseous induction with isoflurane (Abbott, Chicago, USA).
In accordance with the Wani method [ 12], 4 weeks after the suture of the first DMBA implant, the right cheek pouches were everted and then stained with a solution of arecaidine (Sigma Aldrich, St. Louis, USA) at 1 g/L of mineral oil (Aguettant, Lyon, France) with three applications/week.


The in vitro cells
Human lymphocytes and NCI-H460 cells (reference HTB-177 American Tissue Cell Collection) were used for the comet assay. The lymphocytes originated from a lymphoblastoid cell line generated from human blood at the INSERM 614 laboratory (Rouen University, France). The cells were cultured in a RPMI 1640 medium containing 10% fetal bovine serum. The cells were protected from light for the entire duration of the experiment.
The in vivo cells
The cells were collected by swabbing the cheek pouch, suspended in PBS (1 ml), and centrifuged (700 g, 2 minutes, 4°C). The supernatant was withdrawn, and the cells were then re-suspended in PBS (10 5/ml, 4°C). At all time, cells were protected from light exposure.

Fibered confocal fluorescence microscopy

FCFM imaging was carried out with the CellVizio® system (Mauna Kea Technologies, Paris, France). Briefly, the system is made of a laser source, a probe, and a processor. The light bundle was transmitted by the probe, connected to the Laser Scanning Unit (LSU). The probe’s tip was placed in contact with the tissue that was being explored and enabled this tissue to be excited at the LSU's specific wavelength (488 nm or 660 nm). The fluorescent signal emitted by the excited tissue was then collected by the probe, and transmitted to the detector. The system allows to acquire and visualize data as 8–12 images/sec. videos, in real-time.
Two CellVizio® systems were used: one with a LSU emitting at 488 nm, and the other at 660 nm. The power output of the probe when connected to the CellVizio® was 7 mW at 488 nm and 5 mW at 660 nm. The 488 nm source was used for bronchial mucosa imaging with acriflavine, and the 660 nm one was employed for the imaging following local methylene blue application.
Image analysis was performed with the dedicated software MedViewer® 1.1.0. (Mauna Kea Technologies). It allows determining one or two regions of interest (ROI) per lesion, in which cellular density (number of cells/mm 2) and median cellular diameter were assessed. For each ROI, around 100 cells were analyzed.

Hamsters’ cheek pouch imaging

Imaging was carried out under general anesthesia (intra-peritoneal injection of ketamine 30 mg/kg and xylazine 10 mg/kg following gaseous induction with isoflurane), directly on the cheek pouch, which was everted, rinsed with sterile water, and spread on a support (Figure  1B).
Imaging of malignant cheek pouches was conducted after 3, 6, 9, 12, 15 and 18 weeks of exposure to DMBA and performed on areas with macroscopic abnormalities.
For each macroscopic lesion identified, at least one microscopic imaging with CellVizio®, one macroscopic photograph, and one histological examination were carried out.
The fluorophores (500 μl), acriflavine (2.5% mass/volume (w/v)) (Sigma Aldrich, St. Louis, USA) or methylene blue (0.1% or 0.01% w/v) (Aguettant, Lyon, France), were directly pipetted onto the cheek pouch and then rinsed with physiological serum (10 ml). The ProFlex CellVizio® probe was placed on the part of the pouch where the fluorophore had been applied. The cheek pouch was imaged in real time. Between four and five recordings of 5 seconds (40 images per recording) were taken of each cheek pouch.
During imaging, biopsies were taken on the exact areas that were imaged with CellVizio®. The animal was then euthanized using an intra-cardiac injection of 1 ml of thiopental (Hospira, Lyon, France), and the entire pouch was removed. The samples were preserved in buffered formalin (4%, Labonord, Templemars, France).
Histological analysis was performed following staining with hematoxylin–eosin–safran (HES). Histological examination of biopsy samples was considered the gold standard.

The comet assay

The comet laboratory assay protocol was followed (OxiSelect Comet Assay Kit®, Cell Biolabs Inc., San Diego, USA).
The cells (10 5/ml) were exposed to different experimental conditions and then submitted to an electrophoretic field (300 mA, 1 mV/cm) for 30 minutes at 4°C while being protected from light.
The experimental conditions were:
  • application of methylene blue and illumination at 660 nm;
  • application of acriflavine and illumination at 488 nm;
  • application of fluorophore (methylene blue or acriflavine) without illumination;
  • illumination (488 nm or 660 nm) without fluorophore application;
  • neither fluorophore application nor illumination (control).
For each experimental condition, different fluorophore contact (2 or 15 minutes) and illumination durations (1 or 2 minutes) were tested. After 2 or 15 minutes, the cells were centrifuged (700 g, 2 minutes, 4°C) and re-suspended in PBS (10 5 cells/ml, 4°C) twice in order to control the duration of contact between the fluorophore and the cells.
Acriflavine was diluted at 0.025%. Methylene blue was tested at two concentrations: 0.01% and 0.001%.
Following electrophoresis, the cell slides were stained with Vista Green DNA Dye according to the supplier's instructions. The slides were examined using a fluorescence microscope with a FITC filter, and photographs were taken.
The analysis of the images obtained using the microscope was conducted with Image J software (open source, available at http://​imagej.​nih.​gov/​ij/​). For each cell, the Olive Tail Moment, which reflects the degree of DNA fragmentation, and Tail DNA%, which reflects the percentage of DNA damaged, were determined [ 13, 14].

Statistical analysis

Statistical analyses were performed using the NCSS 2007 software (NCSS, LLC, Kaysville, USA).
Tail DNA% and Tail Moment were compared using the Mann–Whitney test.
The cell densities and diameters of each histological grade (obtained with CellVizio®) were analyzed using the Kruskal-Wallis test. Cell diameter threshold values for each histological grade were established by Receiver-Operating curves (ROC), when using either acriflavine or methylene blue. A p value <0.05 was considered significant.


Genotoxicity assessment
Genotoxicity analysis in in vitro cells
  • Genotoxicity of illumination without fluorophore
    Figure  2 (A-B) shows that a 2-min illumination alone on NCI-H460 cells, at 488 nm (A) and at 660 nm (B), did not induce DNA damage.
  • Genotoxicity of acriflavine
    Figure  2C shows that lymphocytes incubated with acriflavine (0.025%) for 2 minutes, in darkness and not illuminated, did not display any DNA damage (absence of comets).
    Figure  2D shows that lymphocytes incubated with acriflavine (0.025%) for 2 minutes and then illuminated at 488 nm for 2 minutes did display DNA damage. Tail DNA% significantly increased when the contact duration with acriflavine was longer, from 83.4% to 88%, at 2 and 15 minutes, respectively (p = 0.021).
    Regarding the H460 cells, the Figure  3 shows that the Olive Tail Moment parameter significantly increased when the contact duration with acriflavine was extended from 2 to 15 minutes, from 5672.9 ± 1376.6 μm to 7496.9 ± 1959.8 μm (p < 0.001). Similarly, Tail DNA% increased from 79.9% to 84.6% (p = 0.045) when the contact duration with acriflavine was extended from 2 to 15 minutes (data not shown).
  • Genotoxicity of methylene blue
    Figure  2 (E,F,G,H) shows that the lymphocytes incubated with methylene blue concentrations of 0.001% (E) and 0.01% (F), without illumination, or after illumination at 660 nm for 2 minutes (G) or 15 minutes (H), did not display any DNA damage.
Genotoxicity analysis in in vivo cells
  • This experiment was carried out on 5 animals.
    Figure  2I shows that the healthy cheek pouch cells collected by swabbing displayed DNA alterations at baseline, prior to fluorophore application and before illumination, which were linked to epithelial keratinization. These cells were thus not used for the in vivo acriflavine and methylene blue genotoxicity testing.
Malignant transformation of the hamster’s cheek pouch
Overall, 53 animals received an implant impregnated with DMBA. One control animal received a silicone implant without DMBA.
The implants were well-tolerated, and the animals did not display any local infection. Twenty-eight animals lost their implant early, and new implants were inserted.
The hamsters did not suffer any weight loss between first implant implementation and the imaging procedure.
Figure  4 shows the histological lesions obtained.
Table  1 shows the histological lesions that were obtained and imaged with CellVizio® according to the duration of carcinogen exposure (number of weeks after first implant insertion).
Table 1
Histological lesions obtained and imaged with CellVizio ® according to carcinogen exposure duration (number of weeks after first implant implementation)
>3 weeks
>6 weeks
>9 weeks
>12 weeks
>15 weeks
>18 weeks
Reserve cell hyperplasia
Mild dysplasia
Moderate dysplasia
Severe dysplasia
This table shows that the number of lesion increases over time exposure (1 lesion at 3 weeks and 19 lesions after 18 weeks), and that the number of severe lesions also increases over time exposure (none at 3 weeks and 4 severe dysplasia and 5 carcinomas after 18 weeks).
In total, 11 carcinoma lesions (7 invasive cancers and 4 in situ cancers), 5 severe dysplastic lesions, 6 moderate dysplastic lesions, 6 mild dysplastic lesions, 24 hyperplastic lesions, 3 granulomatous lesions, and 3 papillomas were observed.
The control animal that received a silicone implant without DMBA did not present any macroscopic modification, and histological examination showed no abnormalities.
Fibered confocal fluorescence microimaging of cheek pouches during carcinogenesis
Cell density
Examples of FCFM imaging of the cheek pouch at different stage of carcinogenesis are displayed in Figure  5, and cellular features according to histological stage and staining are displayed in Figure  6.
FCFM with acriflavine (Figure  6A): cell density increased significantly, from 423 to 1093cells/mm 2 between the stages of hyperplasia and mild dysplasia (p < 0.001), and from 1093 to 2574 cells/mm 2 between the stages of mild dysplasia and moderate dysplasia (p < 0.001).
FCFM with MB (Figure  6A): cell density significantly increased at each stage during progression from hyperplasia to severe dysplasia (p <0.05). Cell density did not differ significantly between severe dysplasia and carcinoma (2055 vs. 2989 cells/mm 2, p = 0.26).
The cell density was significantly higher with acriflavine compared with MB at the stages of hyperplasia as well as mild, moderate, and severe dysplasia (Figure  6A). In carcinomas, there was no difference in cell density using acriflavine or MB aided -FCFM (3240cells/mm 2 vs. 2989cells/mm 2, p = 0.638).
Cell diameter
The diameters measured with acriflavine aided-FCFM were significantly smaller than those imaged with MB in moderate dysplasia (13 μm vs. 36 μm, p < 0.001) and carcinomas (11 μm vs. 14 μm, p < 0.001; Figure  6B), as expected because acriflavine mainly binds to nuclei whereas MB diffuses in the cytoplasm. No significant difference was noted for the other stages.
In acriflavine-FCFM procedures, cell diameters decreased from hyperplasia to severe dysplasia and carcinoma (Figure  6B). However, there was no significant change in diameter between severe dysplasia and carcinoma (10 μm vs. 11 μm, p = 0.366).
Using ROC curve analysis, a diameter threshold <13 μm provided a 88.9% sensitivity and 88.9% specificity for the diagnosis of severe dysplasia and carcinoma using acriflavine-FCFM (Figure  7A).
In MB-FCFM procedures, cell diameters significantly decreased, from 45 μm to 36 μm between mild and moderate dysplasia (p = 0.02); from 36 μm to 11 μm between moderate and severe dysplasia (p = 0.002) ; and from 36 μm to 13 μm between moderate dysplasia and severe dysplasia/carcinoma (p < 0.001). However, the cell diameter appeared significantly larger in carcinomas compared to severe dysplasia (14 μm vs.11 μm, p = 0.001) (Figure  6B).
Figure  7B shows the ROC curve for MB-FCFM diagnosis of “severe dysplasia and carcinoma” lesions. With a cell diameter threshold <30 μm, sensitivity was 94.7%, and specificity was 97%.


In vivo FCFM is a new tool for respiratory epithelium imaging, which is hampered by the need of an exogenous fluorophore in order to observe the epithelial cell layer [ 1- 5, 7]. The development of fluorophores that can be used in humans is therefore a significant advancement. These fluorophores must be both non-irritating and devoid of any short- and long-term toxicity to be used in humans. They should also permit reproducible nuclear and cytoplasmic imaging.
In this experimental study, we have shown that diluted MB did not induce DNA damage when using the illumination conditions of in vivo confocal endomicroscopy (illumination at 660 nm [5 mW] for 1 to 2 minutes). Methylene blue (Methylthioninium chlorure) is available for the treatment of methemoglobinemia. It is provided in ready to use diluted vials, and no effect on health workers is expected if used under standard conditions. MB is widely used in medical studies, intravenously for treatment of methemoglobinemia [ 15], and topically, especially for the harvesting of lymph in cancer surgery [ 16].
In contrast, acriflavine (0.025%) induced considerable cellular DNA damage with illumination at 488 nm for 2 minutes. The percentage of DNA damaged (Tail DNA%) was close to 90% after 15 minutes of acriflavine exposure. This result, which had not yet been published, is directly linked to acriflavine’s DNA intercalating properties.
In humans, confocal endomicroscopy imaging using acriflavine has been performed in the digestive [ 17] and respiratory [ 1] tract. Fuchs has recently used acriflavine for in vivo confocal imaging of normal and diseased respiratory mucosae in humans [ 1]. The concentration of acriflavine used in this study was 0.05%, and imaging was conducted after 2 minutes of fluorophore exposure. Fuchs’s study showed that acriflavine is useful for differentiating normal and cancerous mucosa tissues. However our study shows that, with a lower concentration compared to Fuchs’ study and with identical illumination exposure duration, a significant genotoxic risk exists with acriflavine use. Furthermore the GHS (Globally Harmonized System) has classified the product H340 – “may cause genetic defects” and H350 – “may cause cancer”. Our comet assay results support this, and acriflavine should not be used in humans, particularly in patients already exposed to respiratory carcinogens.
The absence of genotoxicity with MB is reproducible at a concentration of 0.01%, which enables good-quality epithelial imaging of the cheek mucosa. However, it cannot be ruled out that higher MB concentrations and more intense illumination may cause DNA damage [ 18- 20]. Davies tested the genotoxicity of MB at 0.1% in cultured mammalian cells [ 18] illuminated with white light for 2 minutes, revealing significant DNA damage. Certain points need to be clarified: first, in the Davies experiment, the cells in contact with MB were not rinsed, meaning that the duration of contact with the fluorophore was not controlled. By contrast, in our study, the duration of contact between cells and MB was controlled by rinsing the cells. Fluorophore concentrations were also different, as the fluorophore was diluted in PBS. When confocal bronchial imaging with MB is used in humans, the bronchial tree is rinsed immediately after the fluorophore has been applied in situ [ 4, 7]. This precaution appears to be sufficient for the safe conducting of in vivo microconfocal cellular imaging with the CellVizio®.
Second, the illumination intensity used by Davies differed from that used in our experimental protocol. Davies illuminated his cells with “white light” for 2 minutes with an unknown amount of energy. A reduced illumination wavelength of 660 nm was used in our study, delivering 5 mW at the tip of the fibers for 2 minutes. This duration is longer than the illumination produced by CellVizio® during in vivo bronchial endomicroscopic exploration, in which imaging can be performed in a few seconds. Therefore, our results allow us to put forward a safe method for endomicroscopic exploration in humans. Using this method, the mucosa where the fluorophore has been applied is immediately rinsed, and the same area is not illuminated for more than 2 minutes during imaging.
One limitation of our study was the impossibility to test the fluorophore genotoxicity in the in vivo cheek pouch cells, as the keratinization process in itself induced DNA degradation [ 21].
In this study, the use of MB provided reproducible FCFM imaging of the precancerous lesions, comparable to acriflavine. However, unlike acriflavine, MB enabled the imaging of both the cellular nucleus and cytoplasm. In addition, in vivo FCFM data allowed to differentiate low-grade precancerous lesions from high-grade lesions using two distinct parameters, namely cell “diameter” and cell “density”. FCFM imaging with MB was of great value for the diagnosis of high-grade lesions, severe dysplasia and cancer. Se was 95% and Sp 97%, which at least equals acriflavine FCFM imaging results.
This study was carried out on a significant number of lesions. In line with Heller’s data [ 11], after 6 to 20 weeks of carcinogen exposure, 11 carcinoma lesions (7 microinvasive and 4 in situ carcinomas), 5 severe dysplasia lesions, 6 moderate dysplasia lesions, 6 mild dysplasia lesions, and 24 hyperplasia lesions were obtained.
One point worth mentioning is that apparent cell density was greater with acriflavine than with MB. This difference was significant as regards the precancerous stages of hyperplasia as well as mild, moderate, and severe dysplasia (p <0.05), but was no longer so in carcinomas (p = 0.6).
These variations may be explained by the keratin layer covering the cheek mucosa. This layer may hinder fluorophore penetration into the epithelial cells of the underlying strata and therefore hamper imaging with CellVizio®. From the stage of moderate dysplasia onwards, the keratin layer became thinner, and so the dysplastic epithelial cells could be observed more distinctly. It is possible that MB cannot penetrate this keratin layer as well as acriflavine. In “en face” imaging, MB only permitted superficial imaging. Imaging with acriflavine, on the other hand, allowed the cells of several cellular layers to be counted, which may account for the observed variations in cell density.
Cell “density” significantly increased between the low- and high-grade preneoplastic stages during imaging, whether conducted with acriflavine or MB. Skala made similar findings with the cheek pouch model using a confocal multiphoton table microscope, demonstrating a significant increase in nuclear density from healthy to precancerous cheek pouches [ 22]. We went further in our in vivo study, showing an increase in cell density between the successive carcinogenesis stages using FCFM.
In this study, a threshold diameter for diagnosing high-grade lesions such as severe dysplasia and carcinoma was established: 13 μm for cells imaged with acriflavine, and 30 μm for cells imaged with MB. Particularly, MB-FCFM imaging had a sensitivity of 94.7% and a specificity of 97%, for the in vivo diagnosis of “severe dysplasia and carcinoma” lesions using FCFM. These results confirm that nuclear (acriflavine) and cellular (MB) in vivo microimaging was useful for the diagnosis of precancerous lesions and early-stage cancers.
Fuchs has recently demonstrated in humans that applying acriflavine to the bronchial mucosa permitted the differentiation of healthy, inflammatory, and neoplastic bronchial mucosae using confocal endomicroscopy [ 1]. A preliminary study in humans [ 4] has demonstrated that, when combined with autofluorescence endoscopy, confocal endomicroscopic imaging of the bronchial mucosa was also practicable in vivo using MB. These data, as well as the results obtained in this experimental animal study, indicate that it may be possible to use confocal imaging with MB in humans for precancerous and invasive cancer diagnosis without inducing any genotoxic effects. However, since this study was carried in an animal model, the data may not reflect the situation in humans, especially the threshold values.


Fibered confocal fluorescence microscopy is an effective tool that requires local fluorophore application to image the epithelial layer. The experiment demonstrates at least equal diagnostic power for methylene blue as compared to acriflavine, without being genotoxic in the tested conditions. For that reason, MB should be used rather than acriflavin as a fluorophore for pCLE imaging in future studies. Further investigations are warranted in order to assess the role of this new imaging modality in the early detection and treatment of superficial precancerous and cancerous lesions of the respiratory tract.


The authors thank ADIR Association for funding support.
Supported by: ADIR Association (Bois-Guillaume, France).

Competing interests

LT received a grant research from Mauna Kea Technologies (€1000); was invited as speaker at the International Conference on Cellvzio® Users in 2010 and 2011 (no fee) by Mauna Kea Technologies; and travel to the ACCP congress was funded by Mauna Kea Technologies in 2007. LT is listed as co-author on a patent related to pCLE, shared between Rouen University and Mauna Kea Technologies.
MS was invited to attend the International Conference on Cellvizio® Users by Mauna Kea Technologies in 2011; has been member of a Medical Advisory Board for Mauna Kea Tech. (€750). None of the authors has a financial relationship with a commercial entity that has an interest with the subject of this manuscript.

Authors’ contributions

The authors contributed to this work as follows: BO, LT, and MS carried out the conception and design of the study, the acquisition, analysis and interpretation of the microimaging data as well as drafted the manuscript. BO and RS carried out the genotoxicity assessment. BO and LV participated in the histological process and assessment of the cheek pouch lesions. BO and PB participated in the animal and cellular experiments, and in drafting the manuscript. F-XB participated in setting up the animal model. All authors read and approved the final manuscript.
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