Vacharanukrauh Pinyadapat, Meephansan Jitlada, Tangtanatakul Pattarin, Soonthornchai Wipasiri, Wongpiyabovorn Jongkonnee, Serirat Onsiri, Komine Mayumi
Division of Dermatology, Chulabhorn International College of Medicine, Thammasat University, Pathum Thani, 12120, Thailand.
Department of Transfusion Medicine and Clinical Microbiology, Faculty of Allied Health Sciences, Chulalongkorn University, Bangkok, 10330, Thailand.
Psoriasis (Auckl). 2021 Nov 26;11:133-149. doi: 10.2147/PTT.S335913. eCollection 2021.
To identify the narrowband ultraviolet B (NB-UVB)-induced molecular mechanisms that may account for their anti-inflammatory efficacy, gene expression and transcriptome profiling, which were performed using advanced molecular techniques.
This research was conducted on patients with moderate-to-severe plaque-type psoriasis who received NB-UVB treatment. RNA sequencing (RNA-Seq) was conducted to assay the transcriptomes and identify the differentially expressed transcripts that had been enriched during the major pathway analysis.
Clinical improvement of psoriasis by NB-UVB therapy is linked to the suppression of the "immunological signaling pathways" and "cell cycle regulatory, growth and proliferation pathways" which are critical to the pathogenesis of the disease. In addition, these results were further substantiated by demonstrating that NB-UVB therapy has a significant effect on keratinocyte differentiation and affects the regulation of genes and inflammatory mediators that are related to cell proliferation and apoptosis. Moreover, NB-UVB phototherapy is also involved with the downregulation of toll-like receptors signaling in lesional psoriasis.
NB-UVB is an effective treatment for psoriasis. Our study supports the conclusion that the clinical effectiveness of NB-UVB therapy is based on the suppression of a broad range of inflammatory signaling pathways, gene expression of inflammatory cytokines and increased expressions of anti-inflammatory signaling pathways in psoriatic skin. This is the first study that applied advanced molecular techniques to investigate phototherapy as a new key to unlock genetic knowledge and create novel information. Ultimately, the goal is to increase medical knowledge and improve the patient care of psoriasis.
利用先进的分子技术,确定窄谱中波紫外线(NB-UVB)诱导的可能解释其抗炎功效的分子机制、基因表达和转录组谱。
本研究针对接受NB-UVB治疗的中度至重度斑块型银屑病患者进行。进行RNA测序(RNA-Seq)以检测转录组,并鉴定在主要通路分析中富集的差异表达转录本。
NB-UVB疗法对银屑病的临床改善与对疾病发病机制至关重要的“免疫信号通路”和“细胞周期调节、生长和增殖通路”的抑制有关。此外,通过证明NB-UVB疗法对角质形成细胞分化有显著影响,并影响与细胞增殖和凋亡相关的基因和炎症介质的调节,进一步证实了这些结果。此外,NB-UVB光疗还与皮损银屑病中Toll样受体信号的下调有关。
NB-UVB是治疗银屑病的有效方法。我们的研究支持以下结论,即NB-UVB疗法的临床有效性基于对广泛炎症信号通路的抑制、炎症细胞因子的基因表达以及银屑病皮肤中抗炎信号通路表达的增加。这是第一项应用先进分子技术研究光疗作为解锁基因知识和创造新信息的新关键的研究。最终目标是增加医学知识并改善银屑病患者的护理。