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Central European Journal of Immunology
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vol. 39

Clinical immunology
Expression of interleukin-17 in lesions of erythema multiforme may indicate a role for T helper 17 cells

Zeynep Meltem Akkurt, Derya Uçmak, Gül Türkcü, Hatice Yüksel, Kenan Yildiz, Mustafa Arica

(Centr Eur J Immunol 2014; 39 (3): 370-376)
Online publish date: 2014/10/14
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Erythema multiforme (EM) is an acute self-limiting mucocutaneous disorder thought to be a reaction to an infection or drug. It is characterized by a polymorphous eruption [1]. The classic presentation is named EM minor and is often preceded by herpes infections [2]. Histopathological findings of EM include liquefactive degeneration of the basal epidermal cells, necrotic keratinocytes, and lymphocyte exocytosis. Subepidermal clefts and vesiculation may develop secondary to extensive basal cell vacuolar degeneration in some cases. A lichenoid pattern consisting of a mild to moderate lymphohistiocytic infiltrate may be seen at the dermo-epidermal junction. A dermal infiltrate typically shows lymphohistiocytic infiltrate surrounding the superficial and mid-dermal vessels. Numerous apoptotic keratinocytes are seen scattered at various levels throughout the epidermis. Erythema multiforme is considered a prototype of interface dermatitis and a model lesion for acute inflammation with mononuclear cells [3-5].
Erythema multiforme has been established as a disease caused by lymphocytes as the predominant effector cells. The number of CD8+ cells have been described to be more numerous in the epidermis, whereas the number of CD4+ cells have been described to be more numerous in the dermis. An increase in the number of Langerhans cells has also been reported [6]. The generation of auto-reactive T cells that target the epidermis plays an important role in the pathogenesis of EM. The stimulus in this process is thought to be the expression of HSV DNA fragments in the skin [7]. Presumably, viral DNA and proteins ingested by macrophages at HSV lesion sites undergo fragmentation and processing for presentation to T cells with HSV memory. HSV DNA encoding the viral DNA polymerase (Pol) is deposited on the skin by circulating CD34+ hematopoietic progenitor cells [8], which transport it from the site of the original HSV lesion, and then it is expressed. Activated T cells are recruited to the skin at sites of Pol expression, directly or indirectly resulting in the generation of an inflammatory cascade [9]. These are mainly CD4+ T cells characterized by a T helper type 1 (Th1) response, which promotes the expression of IFN-γ and transforming growth factor  (TGF-) [10, 11]. Erythema multiforme, to a lesser extent, may be drug-induced. Although clinically similar, histopathologically, the inflammatory response in this scenario consists primarily of non-T and CD8+ T cells [6] and the expression of tumor necrosis factor  (TNF-) [10].
Since the description of a distinct subset of T cells, T helper type 17 lymphocytes (Th17), substantial evidence has emerged on their involvement in various autoimmune diseases.
In this study, we aimed to determine the serum cytokine profile of patients with EM. We assumed the presence of a Th1 cytokine profile but in addition we aimed to determine serum IL-17A levels and search for the presence of IL-17A-secreting cells in lesional samples.

Material and methods


This study was conducted at the Dicle University Faculty of Medicine and Diyarbakir Training and Research Hospital Dermatology clinics on patients diagnosed with erythema multiforme, either of the minor or the major subtype, from March 2012 to January 2013. The patients’ lesions were biopsied and blood samples were obtained from the patients and from healthy control subjects. Informed consent was obtained from the subjects participating in the study. Approval of the Ethics Committee of Dicle University was obtained and the study was performed in accordance with the ethical standards laid down in the 1964 Declaration of Helsinki and its later amendments. Erythema multiforme with mucosal involvement was classified as erythema multiforme major and in the absence of mucosal disease, the disease was classified as EM minor [3]. All patients had active disease at the time of sample collection.

Blood samples

Venous blood samples were obtained and immediately centrifuged. Serums were kept at 80°C until laboratory testing. The serum interleukin (IL)-2, IL-6, IL-8, interferon γ(IFN-γ) (Invitrogen, Camarillo, CA), IL-10 (Invitrogen, Frederick, MD, CA) and IL-17A (Biosource Europe S. A. Belgium) levels were determined using the enzyme-linked immunosorbent assay method according to the manufacturer’s protocols. Serum samples from 29 age- and sex-matched healthy controls were obtained and used for comparison.


Biopsy samples were obtained using 4 mm punch biopsy blades. The non-necrotic peripheral areas of the lesions were sampled, avoiding the central necrotic or bullous parts of the lesions.
The punch biopsy materials were fixed in 10% formalin solution for 24 hours. After biopsy material from each patient was processed by routine histological tissue preparation, all specimens were embedded in wax. 4 µm sections of tissue were transferred from paraffin-embedded blocks to four positively charged slides one of which was stained with HE. The other three were stained with CD4 (sc-7219, Santa Cruz Biotechnology), CD8 (C8/144B, Cell Marque) and IL-17 (sc-7927, Santa Cruz Biotechnology) antibodies using an automated immunohistochemical staining device (Ventana Benchmark XT). Samples of human tonsillar tissue and normal skin were used as positive and negative controls, respectively. All samples were reviewed by the same pathologist using a light microscope (Nicon Eclipse 80i) and the results were reported as the percentage of stained cells among the inflammatory infiltrate.

Statistical methods

Statistical analyses were performed using SPSS 15.0. Mann Whitney U test was used for the analysis of the data. Correlation analyses were done using Spearman’s correlation analysis. A p value < 0.05 was considered to be significant.



A total of 32 patients (22 females and 10 males) diagnosed with EM of the minor or major type were included in the study. 29 patients had EM minor and three patients had EM major. The patients’ mean age was 30.56 ±2.59 (range 14-72). Blood samples were obtained from 23 patients and biopsy samples were obtained from 30 patients.
The mean duration of the lesions was 5.73 days. Eleven patients reported that this was their first attack. The rest had had previous attacks. Twenty-two patients had a preceding attack of herpes infection of mean 12.91 days ago. A mean duration of 7.95 days had passed from the onset of herpes to the onset of EM. Five patients reported sun exposure before the attack of EM. Two patients linked their lesions to the preceding upper respiratory tract infection and use of medicine. The three patients with EM major and two patients with EM minor were treated with systemic steroids. The rest were treated with topical steroids.

Blood samples

The mean age of the patients who donated blood samples was 30.59 ±12.40 (range 14-62).
The controls’ mean age was 29.97 ±2.43 (range 18-70) and the difference between the two groups was not statistically significant (p = 0.561). The patient group consisted of 15 females and eight males and the control group consisted of 20 females and nine males.
Mean cytokine values of the patients and controls and p values are shown in the Table 1. Levels of IL-2, IL-6, IL-8, and IL-17A were significantly higher and IL-10 was significantly lower in the patient group. Levels of IFN-γwere not different among the patients and the controls. There was an inverse correlation between levels of IL-17A and IFN-γ (r = –0.413 and p = 0.045) and IL-10 and IFN-γ (r = –0.511 and p = 0.013) in the patient group. There was an inverse correlation between duration of the lesions and levels of IL-10 (r = –0.441 and p = 0.045). Levels of the measured cytokines were not significantly different between patients with and without recurrent lesions.


Hematoxylin and eosin staining demonstrated typical histopathologic findings of EM in all specimens (Fig. 1). The most frequently observed findings were (in a decreasing order) the presence of a lichenoid reaction, vacuolar changes, lymphocyte infiltration in the superficial dermis, epidermal lymphocytes, subepidermal clefts and apoptotic cells. There was a band-like and perivascular infiltration of lymphocytes in the superficial dermis.
On IHC, 50-90% (mean 73.5%) of the lymphocytes in the samples were stained with CD4, 10-50% (mean 26.5%) were stained with CD8. Interleukin 17-expressing cells were observed in all samples, with their proportions in the infiltrate being 5-15% (with the exception of one case with 50% staining, mean 9.33%) (Figs. 2-4).


The results of this study indicate that levels of IL-2, 6, 8 and 17A were significantly higher in the patient group compared to the control group and levels of IL-10 were significantly lower than in the control group. The presence of a CD4+ T lymphocyte predominance in lesional tissue was observed. In addition, 5 to 50% of cells in the infiltrate were found to express IL-17.
Increased serum IL-2 is in agreement with the expected Th1 cytokine profile in EM. IL-2 promotes the proliferation of T cells and is among the main Th1 cytokines [12]. It has previously been demonstrated to be increased in the serum of patients with EM [13]. Interferon γ, one of the major Th1 cytokines, was not elevated in the sera of the patient group in our study. IL-10 is a cytokine involved in the development of regulatory T cells and also is an effector of Th2 responses [12]. One study has reported that its levels were increased in EM [14] but our results have turned out the opposite. The increased serum IL-6 and IL-8 levels lead us to think that the localized lesions of EM may be accompanied by a systemic reaction involving a whole array of cytokines, besides those of the Th1 type. Patients with EM minor predominated our patient profile, with the exception of three who had EM major. Statistically, it was not possible to make a comparison between these two types, but the results of the patients were again significant compared to the controls when the cases with EM major were excluded. The increase in serum levels of IL-17A might indicate an active Th17 response in EM. Increased IL-6 is also supportive of this, since IL-6, along with increased TGF-, promotes development of the Th17 cell line [15].
It has previously been established that EM is a Th1 cytokine-dominant reaction in which CD4+ T lymphocytes predominate [6]. CD4+ T lymphocytes were the majority of the inflammatory infiltrate in our patients, with lesser numbers of CD8+ cells. The characteristics of the infiltrate and cytokine milieu in SJS/TEN are different than EM and will not be discussed in this paper. The Th1-related cytokines IFN-γ and IL-2 were found to be expressed lesional specimens of EM, whereas TNF- has been found to be weakly expressed [16]. According to our knowledge, this is the first demonstration of the presence of IL-17-expressing cells in lesional samples of EM. The exact nature of these cells is yet to be determined. Interleukin 17A is among the main secretory products of Th17 cells, but other cell types such as γ-T cells, CD8+ T cells, eosinophils, neutrophils and monocytes may also produce the cytokine [17]. We were not able to determine the exact nature of the cells expressing IL-17 in our study, but the possibility of them being Th17 cells is exciting enough to ponder on a wide array of possibilities.
The discovery of Th17 cells has damaged the orthodox view of the Th1/Th2 paradigm in immunology and it appears that this cell line is distinct from the mentioned subtypes of T helper cells. Although it is distinct, this cell line does not exist as the sole predominator of pathogenic T lymphocytes in a disease, but may be a cause, or the result of the ongoing process and co-exist with other T cell populations. In fact, Th17 cells and their cytokines may be important regulators of innate and adaptive immune responses in many Th1 and/or Th2-mediated diseases [18]. Th17 cells produce a group of cytokines including IL-17A, IL-17F, IL-21, IL-22, TNF-, and IFN-γ, in addition to IL-26 and chemokine ligand (CCL) 20 [19]. Interleukin 17 is important in the commencement and maintenance of autoimmune reactions and in production of proinflammatory cytokines, matrix metalloproteinases, neutrophils and eosinophils [20]. Either the presence of lesional IL-17-secreting cells or Th17-related serum cytokines has been demonstrated in various autoimmune and/or inflammatory diseases, such as psoriasis [21, 22], psoriatic arthritis [23], palmoplantar pustulosis [24], Behçet’s disease [25], bullous pemphigoid [26], pemphigus vulgaris [26], systemic sclerosis [27] and vitiligo [28]. Besides their proposed proinflammatory role in various diseases, the Th17 cell line is crucial in protection against bacterial and fungal pathogens and is thought to be a part of host defences at the epithelial surfaces and potent in the recruitment of neutrophils [29, 30]. Their role in EM remains to be elucidated, though. A recent study has shown the presence of IL-17-secreting CD4+ lymphocytes in sera and blister fluid of patients with SJS/TEN and EM major. They reported that the proportion of IL-17-secreting CD4+ cells in the serum of SJS/TEN was higher than the controls. Although the difference was not significant when patients with EM major were compared to the controls, the number of patients in this study is quite few [31].
Th17 cells are activated CD4+ T cells. The orphan nuclear receptor RORγt, a key transcription factor which induces the transcription of genes encoding IL-17A and IL-17F in naïve CD4+ T helper cells. IL-6 and TGF- are the cytokines known to induce this cell line [15]. It has been reported that HSV type 1 and type 2 are potent inducers of IL-6, and this phenomenon is augmented in the presence of IFN-γ [32]. Transforming growth factor  is expressed in lesions of EM [10]. Thus, the possibility comes to mind that Th17 may be formed de novo in EM. On the other hand, it has become clear that the Th17 lineage is not a single distinct lineage, but rather encompasses several T lymphocytes which all produce IL-17A, but possess varied effector functions. In fact, not all IL-17-producing T lymphocytes are pathogenic [19]. T-lymphocytes which are IFN-γ + and IL-17+ originate from IL-17-producing Th17 cells, and are closely associated with pathogenicity [33]. It has previously been stated that C. albicans and S. aureus prime Th17 cells produce either IFN-γ or IL-10 by eliciting different cytokines [34]. Interleukin 1 and IL-2 are pro- and anti-inflammatory regulators of TH17 cells both at priming and in the effector phase [34]. Interleukin 1 is a cytokine released from keratinocytes and has previously been linked to inflammatory skin disease. Th17 cells possess its receptors and secrete cytokines in response [35]. Instead of de novo formation, Th17 cells may be transformed into the more pathogenic IFN-γ-secreting types in EM. Although the differentiation of naïve CD4+ T cells has been viewed as an irreversible event and it is generally believed that fully differentiated Th1 cells have little or no plasticity to be redirected to become Th17 cells, it has been demonstrated that HSV-specific Th1 clones were still capable of producing IL-17 upon superantigen stimulation [36]. It might be possible that HSV-specific Th1 cells may be triggered by superantigen stimulation to produce IL-17. The IL-17-expressing cells in our samples may be of this type. A study supporting this idea has shown that superantigenic S. aureus stimulates IL-17 production from CD4+ T cells of adults with memory phenotypes but not from naïve CD4+ T cell phenotypes [37].
The association of HSV and Th17 cells has been studied in detail by Suryawanshi et al. in a study in which they studied a mouse model of corneal herpes infection leading to stromal keratitis, a chronic inflammatory reaction of the cornea to infection by herpes. Their data demonstrated that Th1 cells mainly initiate and orchestrate the lesions during the early stages, followed by the later entry of Th17 cells when the disease was at peak. The late entry of Th17 cells was partly explained by the delayed upregulation of IL-6 and TGF-, cytokines responsible for Th17 generation, as well as CCL20 expression in the cornea, a chemokine responsible for the migration of Th17 cells at the site of inflammation [38]. The authors commented that the body might sense the chronic persistence of antigen in HSV infections and as the need arises for stronger and more pathogenic immune response for the removal of such persistent antigen, the production of IL-17-producing cells or Th17 cells may be stimulated. This theory might explain the frequently detected presence of Th17 cells in autoimmune diseases and might be put to use in the pathogenesis of EM, where the chronic persistence of HSV DNA may presumably trigger a diversion of the Th1 responses to a Th17 direction. It is not known whether IL-17A is increased in the serum in between attacks in patients with recurrent EM, or whether the latent HSV infection itself is the trigger for the production of Th17 cells and IL-17A. In addition, the presence of other cytokines of the Th17 cell line, i.e. IL-21, 22 and 23 has not been investigated in EM. The presence of Th17 in an assisting role or an auto-reactive and possibly damaging (i.e. severe recurrent EM major) role is yet to be determined. The elucidation of the role of the Th17 axis in EM may shed light on the HSV and immune system interaction. A role for the Th17 axis in EM also brings to mind the possible therapeutic use of inhibitors of IL-17 and/or IL-23 in severe or recurrent cases of EM. At present, phase II and/or III trials of IL-17 inhibitors such as secukinumab, ixekizumab and brodalumab in the treatment of various diseases such as psoriasis, rheumatoid arthritis and Crohn’s disease are being conducted. The effectiveness of these agents in the treatment of EM may be investigated [39].
The administration of small interfering RNA to mice with BD led to a decrease in the previously increased levels of IL-6 and improvement in BD symptoms. The serum levels of IL-17 also decreased (though the difference was not significant) and Foxp3+ regulatory T cells (Tregs) in these mice were more numerous compared to those in which IL-6 had not been inhibited [40]. Tregs, yet another cell line of the CD4+ T cell lineage, are a critical cell line in prevention of immune responses directed against self-antigens. It is known that Tregs efficiently suppress the effector functions of Th17 cells and it has been suggested that Treg-based therapies will be effective for Th17-mediated pathologies [19, 41]. It is necessary to question the role of Tregs and a possible deficiency in their responses in EM.
A limitation of this study was that serum cytokine levels were not reassessed after remission of lesions. Another limitation was that the exact nature of the IL-17A-secreting cells in the infiltrate could not be determined.


The discovery of specific cell types involved in EM and their links to HSV may advance our knowledge on important links between HSV and the immune system. As more knowledge on the subject is attained, novel therapies targeting key steps may be developed.

This project was supported by grants from the Dicle University Scientific Projects Commission (grant number: 12-TF- 130).
The authors declare no conflict of interest.


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Copyright: © 2014 Polish Society of Experimental and Clinical Immunology This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License (http://creativecommons.org/licenses/by-nc-sa/4.0/), allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
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