The ethiopathogenesis of psoriasis is complex, multifactorial and still not well understood. Nowadays, the systemic, inflammatory and autoimmunological aspects of psoriasis are being emphasized [1].
Toll-like receptors (TLR) are characterized as pattern-recognition receptors, which are capable of potently activating various cell types. Toll-like receptors downstream signalling pathways lead to the production of a wide range of immune stimulatory cytokines and chemokines. Aberrant activation of TLR may result in an unrestricted inflammatory response, so the receptors may play a role in the development of inflammatory and autoimmune disorders [2].
TLR1, 2 and 5 are constitutively expressed on the normal keratinocytes [3]. TLR1 and TLR2 expression is further upregulated in psoriatic lesions [3, 4]. Seung et al. found a higher expression of TLR4 in guttate psoriasis compared to the plaque type and controls [5]. Moreover, TLR5 and TLR9 were upregulated by transforming growth factor α (TGF-α) in psoriatic keratinocytes [6]. In another study, Begon et al. showed the expression of tumor necrosis factor α (TNF-α) and interleukin (IL)-8 induced by the TLR2, 3 and 4 signalling pathway via nuclear factor κB (NF-κB) nuclear translocation in psoriatic keratinocytes [7].
In the light of these facts, TLR genes seem to be interesting gene candidates involved in psoriasis pathogenesis.
In this study we clarified the effect of Arg753Gln TLR2 and –1237 T/C TLR9 gene polymorphisms on the risk and the clinical manifestation of psoriasis.
The study group consisted of 175 unrelated patients with psoriasis vulgaris and 170 healthy, unrelated, age- and sex-matched volunteers. The mean Psoriasis Area Severity Index (PASI) was 16.9; PASI > 10 was observed in 90 patients. In the study group there were 121 (78.1%) patients with early onset (< 40 years) and 39 with late onset psoriasis (≥ 40 years). The gene polymorphisms were analyzed using the amplification refractory mutation system polymerase chain reaction method (ARMS-PCR).
There was no statistically significant association between genotype and allele frequencies in psoriatic patients in comparison with controls (Table 1). However, the presence of allele G in Arg753Gln TLR2 polymorphism was statistically more frequent in the group with late onset psoriasis in comparison with early onset psoriasis (100% vs. 96.2%; p = 0.0127). The presence of allele T in –1237 T/C TLR9 polymorphism was more common in the group of early onset psoriasis (86.3% vs. 73.8%; p = 0.0086) and their presence increases more than twice the risk of the development of this type of the disease (OR = 2.23, p = 0.098). Moreover, TT –1237 T/C TLR9 genotype polymorphism was statistically more frequent in patients with PASI score > 10 (78.13% vs. 63.04%; p = 0.035). In the group of patients with PASI score > 15 TT genotype was also more frequent (79.66% vs. 68.67%; p = 0.38).
Table 1.
Genotype and allele frequencies for Arg753Gln TLR2 and –1237 T/C TLR9 gene polymorphisms in control subjects (n = 170) and patients with psoriasis (n = 175)
| Genotypes and alleles | Controls | Psoriasis | p-value |
|---|---|---|---|
| Arg753Gln TLR2 | N = 170 | N = 175 | 0.67 |
| GG | 162 (95.3%) | 165 (94.3%) | 0.67 |
| GA | 8 (4.7%) | 10 (5.7%) | 0.67 |
| AA | 0 (0.0%) | 0 (0.0%) | |
| N = 340 | N = 350 | ||
| G | 332 (97.6%) | 340 (97.1%) | 0.68 |
| A | 8 (2.4%) | 10 (2.9%) | |
| –1237 T/C TLR9 | N = 170 | N = 175 | 0.39 |
| TT | 135 (79.4%) | 128 (73.1%) | 0.36 |
| TC | 26 (15.3%) | 35 (20.0%) | 0.47 |
| CC | 9 (5.3%) | 12 (6.9%) | 0.64 |
| N = 340 | N = 350 | ||
| T | 296 (87.1%) | 291 (83.1%) | 0.14 |
| C | 44 (12.9%) | 59 (16.9%) |
The true impact of the TLR polymorphisms on psoriasis susceptibility and course still remains unclear. In our research the study group was divided into early and late onset psoriasis due to epidemiological, genetic, immunopathological and clinical dissimilarities associated with these two types of the disease. Despite the fact that our results have not shown any association between TLR polymorphism and psoriasis susceptibility, we demonstrated the potential influence of these polymorphisms on clinical disease presentation. Romani et al. [8] found a relationship between TLR9 –1486 T/C SNP variants and a better response to narrow-band UVB phototherapy. Individuals bearing TC or CC genotypes showed a higher improvement of PASI score compared to patients with TT genotype. The TLR9 activation prompts an inflammatory pathway driven by interferon and IL-12 [8]. The blockade of TLR9 has been proposed also as a potential therapeutic target in psoriasis vulgaris [9].
In conclusion, the presented data do not prove the pathogenetic role of TRL2 and TLR9 polymorphisms in psoriasis development, however, they may have influence the clinical course of the disease. Further investigations are strongly required.
Acknowledgments
The study was funded by the Medical University of Gdansk (project no. 02–0066/07).
Conflict of interest
The authors declare no conflict of interest.
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