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Journal of Clinical Medicine Research

Review

Volume 7, Number 6, June 2015, pages 393-399

Photodynamic Therapy in Treatment of Oral Lichen Planus

OLP is a relatively common chronic, immunologic, inflammatory, mucocutaneous disorder. It affects 0.5-2% of general population. It has higher incidence in females with no racial predisposition. It affects middle-aged patients (over 35 years) while children and teenagers are rarely affected. Oral form of lichen planus occurs more frequently and tends to be more resistant to treatment than cutaneous form. Approximately one-third of the patients who have oral lesions also have skin lesions [1-8].

There are several hypotheses involving genetic, infectious, psychogenic and autoimmune factors [9]. Recently, it was accepted that OLP involves chronic cell-mediated immune reaction of unknown etiology that induces damage to basal cell layer of the epithelium, in which T lymphocytes accumulate in the superficial lamina propria, basement membrane (BM) disruption, intra-epithelial T-cell migration and keratinocyte apoptosis in OLP [10, 11]. It was reported that patients with OLP have higher levels of stress, anxiety, and depression. Elevations of salivary cortisol (stress hormone) and psychological factors have been found in OLP patients. It was also found that local conditions such as poor oral hygiene and smoking may exacerbate OLP [9, 12-15]. Also, there are many reports of association between erosive OLP and infectious agents: herpes simplex virus (HSV), Epstein-Barr virus (EBV), human papilloma virus (HPV), cytomegalovirus (CMV) and human immunodeficiency virus (HIV). It could be due to the persistence of infection in the epithelial cells affected with viruses [13, 16, 17].

A number of previous reports have suggested that patients with OLP have associated diabetes, hypertension and liver diseases more often than patients without OLP [18, 19]. Conversely, some reports have not supported these presumptions [20]. Also, more than 90 controlled studies had reported association between OLP and hepatitis C virus [13, 16, 21]. The probable reason is the ability of HCV-RNA for cytopathic replication outside the liver cells, persistent infection and triggering of immunological processes (the activated CD8 T cells, cytokines and expansion of certain B-cell clones), leading to OLP manifestations [22]. The CD8⁺ T cell proportion of OLP-HCV patients in lamina propria was significantly higher and deeper than in OLP which gives the more aggressive erosive manifestation of OLP-HCV patients [23]. On the other hand, this association was not confirmed by Dupin et al [24], who stated that there was no association between OLP and HIV.

OLP has characteristic clinical features and distribution in the oral mucosa. It is commonly presented bilaterally on posterior buccal mucosa but not always symmetrical. OLP lesions are characterized by periods of exacerbation and remission [25, 26]. The OLP lesion is based on six clinical forms that were described by Andreason [27] as reticular, papular, plaque, atrophic, erosive, and bullous. The same patient may have OLP with multiple forms [28]. Reticular OLP is the most common form that is characterized by asymptomatic interlacing white keratotic lines called Wickham’s striae where it does not disappear by stretching or rubbing its surface [29]. Erosive OLP is a mix of erythematous and ulcerated areas. Atrophic OLP is diffuse erythematous patches of mucosal thinning and combined with striae. Bullous OLP has intraoral bullae that rupture soon after their appearance, causing painful ulcerated surface. Plaque OLP is described as homogenous white patches looking like oral keratosis. Papular OLP contains small white papules with fine striae [27]. The cutaneous lesions can be described as shiny, well-defined, purplish, polygonal, planar, pruritic papules and plaques that may reveal white striations (Wickham’s striae). The flexor surfaces of the legs and arms, especially the wrists are the most common sites [30, 31]. Malignant potential of OLP is estimated 0.4-6.25%. Only lesions that have dysplasia are potentially at risk of developing into cancer. Smoking and alcohol may increase the risk of oral cancer [32-34]. The incidence of squamous cell carcinoma is higher for females. The malignant transformation occurs most frequently in the erosive form of OLP 35%, followed by the plaque type 24% and the reticular type 11% [35-37].

Due to the partially understood pathogenic mechanism and potential malignant nature of OLP [32], various modalities are done for treatment of the symptomatic OLP. The aim of these modalities is to reduce the length and severity of symptomatic outbreaks [30]. Follow-ups and periodic examinations are needed to avoid any possible malignant transformation [35, 38].

Lasers have been suggested as non-pharmacological modality to patients resistant to conventional treatment but their effectiveness is under study [39]. Lasers are used in high- or low-level laser irradiation manners for treatment of OLP. Some studies have conducted that high-level lasers are used for successful OLP tissue ablation such as CO₂ lasers which have been proven to be very effective treatment for OLP with decreasing recurrence rate 20% in which the thermal laser energy carbonizes superficial layers of epithelium [40, 41].

However, low dose 308-nm excimer laser is a palliative treatment when the mucosa lacks the overlying epithelial layer, and a higher and more effective UV dose is allowed to reach the infiltrating lymphocytes [42]. Diode laser 980 nm was also reported as an easy, effective, fast and safe treatment of OLP [39].

Photodynamic therapy (PDT) has been reported as a very promising treatment method as it does not cause scarring because of the eradication of microfoci after PDT, which cannot be seen upon macroscopical examination. It also decreases risk of recurrence [43, 44].

PDT is a recent therapy that began to be explored in treatment of OLP. It is a special type of treatment that combines two components: a photosensitive agent or photosensitizer (PS) and a harmless light source of a specific wavelength [45]. The visible light irradiation forms biochemical interactions in the presence of the PS which undergoes excitation and produces toxic oxygen species such as singlet oxygen and free radical that cause specific cellular destruction, membrane lysis and protein inactivation [46-48]. Nowadays, PDT is used for the treatment of various types of oral diseases such as cancers, leukoplakia, erythroleukoplakia, dysplasia, and mucosal hypertrophy. Its efficacy varies, from complete regression of lesions to the lack of response to treatment [49].

PDT PSs are chemical compounds that can be promoted to an excited state upon absorption of the light. When they capture light energy, they transfer it into chemical reaction in the presence of molecular oxygen produces singlet oxygen (¹O₂) or superoxide (O₂^-), which gives them the ability to induce cell damage through direct and indirect cytotoxicity [50, 51].

PSs can be classified by their chemical structures and origins into three broad families: 1) porphyrin-based PS (e.g. photofrin, 5-aminolevulinic acid (ALA/PpIX), BPD-MA), 2) chlorophyll-based PS (e.g. chlorins, purpurins, bacteriochlorins), and 3) dye (e.g. phtalocyanine, napthalocyanine). Most of the currently approved clinical PSs belong to the porphyrin family [51].

The first PSs used in PDT were compounds belonging to the group of hematoporphyrin, photofrin, and meta-tetra (hydroxyphenyl) chlorin. After extended period of time, the PSs of choice included ALA and dyes - toluidine blue and methylene blue (MB) [52].

Methyl 5-aminolevulinate (MAL) is an esterified derivative of ALA. It is lipophilic and its selectivity for specific cells is greater than that of ALA which increases its phototoxicity effect [53].

The phenothiazine dye MB has excellent photochemical properties and is recognized as non-toxic dye. Unlike other PSs, it can be administrated topically and orally, which make it the preferred choice for superficial lesions in skin and oral cavity [54-56]. It also has high absorption of wavelengths at 665 nm, where light penetration into the tissue is optimal [54, 57, 58]. It has a natural antifungal and antibacterial activity, of which toxic potential can be increased by light activation [54, 55, 59].

Photolon^®, a novel chlorine 6-derived PS, is a pigment that has been successfully substantiated with evidence in the treatment of precancerous, cancerous lesions [49, 60, 61], and it had produced advantageous outcomes in OLP treatment, reducing the main signs and symptoms even without the need for analgesics or anesthetics during PDT which make it suitable choice of treatment for the old patients [49].

However, until this moment, there is no PS that would have all clinical demands. Most of them have disadvantages like: prolonged skin photosensitivity, limited ability of cell selectivity, and unpredictable efficacy [57].

Various light sources are used in topical PDT. 1) Lasers are considered as an ideal light source for PDT due to its coherence and monochromaticity. The therapy of soft tissue performed with such lasers is called “low level laser therapy” (LLLT) [62]. Nowadays, diode lasers are commonly used in clinics. They are compact and portable. They have a high conversion efficiency from electrical energy to laser energy [62-64]. 2) Lamps have been useful in PDT especially in the cure of skin diseases such as metal halogen lamp and short arc xenon lamp. Although the light is filtered, the wavelength bands are wide compared with the absorption bands of the photosensitizing substances which lead to heat release that causes the cytotoxic effect [63]. 3) Lasers emitted diodes (LEDs) generate wavelength bands wider than those from lasers [63].

This treatment is done in two stages. In the first stage, the photosensitizing agent is accumulated in the target cells (rapidly dividing cells) that need to be treated, following topical administration. This was explained by disproportionately of high numbers of low density lipoproteins receptors of their cell membranes and abnormal microvasculature [65]. However, not only this type of tissues exhibit accumulation of PS but also there are microorganisms like bacteria, fungi and viruses exhibiting selective accumulation of PSs due to differences in permeability of their outer structures. In addition, several normal body tissues exhibit the same phenomenon which is not well understood [65, 66].

While in the second stage, the photosensitized cells are exposed to light source of specific wavelength that coincides with the absorption spectrum of the PS. The second step is: a measured light dose of appropriate wavelength is then used to irradiate the target tissue [67, 68]. This light activates the dye and elicits a series of cytotoxic reactions. It causes the generation of reactive oxygen species (ROS) that has toxic effect on target cells [69-71].

PDT produces cytotoxic effects by three mechanisms: cellular, vascular and immunological responses. Combination of these responses depends on the tissue oxygen availability, the PS and the illumination scheme used [72, 73].

When PS localizes in cell membranes, it causes interruption and damage to plasma membrane that may release harmful proteins and chemicals. Then, it causes damage to adjacent cells [74]. PSs which are localized in mitochondria produce cell death via apoptosis, while those localized in lysosomes and plasma membranes induce cell death predominantly by necrosis [75]. They do not accumulate in the nucleus which makes them have low potential to generate DNA mutations or carcinogenic effect [75]. Changes in vessel diameter, platelet aggregation and leakage of vessels during PDT cause the formation of edema [76, 77]. This causes indirect damage by the deprivation of oxygen and nutrients which affects the effectiveness of PDT. Without the availability of oxygen and singlet oxygen, PDT cannot be induced [72, 76, 77]. Also PDT affects the immune system and cytokines, chemokines and other biological response modifiers are released. The inflammatory cytokines interleukin IL-6 and IL-10 but not TNF-α have been discovered to be regulated after PDT. Also, neutrophils were increased in number after PDT [76, 78-80].

The treatment of symptomatic OLP represents a therapeutic challenge. Despite numerous existing remedies, some of these treatments are failures. Recently, the use of PDT has been expanding due to its numerous advantages, as it is safe, convenient and non-invasive as it has selective toxicity towards target tissues. It has also excellent cosmetic results, where healing produced with little or no scarring. It can be repeated without producing any harm to normal tissues and can be used alone or in conjunction with other treatment [81].

Aghahosseini et al [52] in 2006 estimated that PDT is an alternative method for the treatment of OLP in 13 patients with 26 mucosa lesions. The patients rinsed with 5% aqueous solution of MB dye for 5 min. After 10 min, the lesions were exposed to a low-energy laser of 632 nm wavelength and exposure dose of 120 J/cm² (Table 1). Sixteen lesions were improved and four lesions had complete remission. The mean reduction in the size of lesions was 44.3%. The same author published in another research of case report, the application of PDT mediated by MB in two patients had five lichen planus lesions (Table 1). Two lesions completely disappeared, two lesions were improved 50% clinically and one lesion had no response [82].

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Table 1. The Published Clinical Researches of Photodynamic Therapy in Treatment of Oral Lichen Planus From 2000 to 2014

Sadaksharam et al [48] in 2012 (Table 1) conducted a research on 20 patients with systemic OLP. The patients were treated by PDT using xenon arc lamp of 630 ± 5 nm wavelength and total dose of 120 J/cm² per sitting in four sessions mediated by MB. They achieved a significant reduction in lesions over prolonged period without any side effects. This was also supported by Sobaniec et al [49] who concluded that there were no adverse effects during PDT or during the follow-up periods.

Sobaniec et al [49] (Table 1) obtained a clinical study on 23 patients with 48 lesions treated with PDT using gel containing 20% chlorine-e-6 Photolon^® and 10% dimethyl sulfoxide which was applied directly onto the lesion and the surrounding healthy mucosa 1 h before exposure to a semiconductor laser with wavelength 660 nm. A series of illuminations were performed using light energy density of 90 J/cm². The appointments were scheduled at 2-week intervals, but no longer than for 10 sessions. They concluded that PDT could be useful in treatment of OLP where the size of clinical lesions in patients decreased significantly in 55%, and the best effects were observed on lining mucosa more than masticatory mucosa.

Sobaniec et al [49] and Aghahosseini et al [52] (Table 1) had used the diode laser with the same wavelength and energy density but different PSs but Aghahosseini et al [52] estimated that the significant improvement of signs and symptoms was after 1 week of a single session of PDT and during the follow-up period (up to 12 weeks). This was confirmed by Kvaal et al [83] who conducted a clinical study on 14 patients treated by PDT mediated by a porphyrin, MAL (Table 1). The OLP lesions were illuminated by diode laser with wavelength of 600 - 660 nm and energy density of 75 J/cm² to treat OLP patients for 6 months. They reported remarkable lasting improvement after a single treatment, and even during 4 years of follow-up, without any side effects [83, 84].

In conclusion, the main outcome of comparing the clinical studies is that the PDT is considered as a safe and effective advanced treatment modality for OLP. PDT is giving a remarkable effectiveness and improvement evidences in treatment of OLP where the selected articles demonstrated a significant reduction in the signs and symptoms of OLP and an increase in the symptom-free periods.

Due to the confined number of relevant published data of PDT, limited sample size and short follow-up periods, we could not give definite evidence for the advantage of PDT in treatment of OLP. More clinical studies and verifications with randomized clinical trials, larger numbers of patients and long follow-up periods are needed to evaluate the effectiveness of PDT in treatment of OLP.

Conflict of Interest

There is no conflict of interest.

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