Jeong Soyoung, Shin Sanghee, Choi Hyun Seung, Choi So-Jung, Jang Sehun, Song Jeongmin, Lee Ji Su, Lee Dong Hun, Kim Hyun Je, Kim Jihyun, Ahn Kangmo
Department of Biomedical Sciences, Seoul National University Graduate School, Seoul 03080, Korea.
Department of Pediatrics, Chung-Ang University Hospital, Chung-Ang University College of Medicine, Seoul 06973, Korea.
Immune Netw. 2025 Jun 20;25(4):e26. doi: 10.4110/in.2025.25.e26. eCollection 2025 Aug.
Pediatric atopic dermatitis (AD) shows distinct clinical characteristics compared to adult AD, suggesting unique inflammatory profiles that may influence disease prognosis and treatment response. We aimed to identify unique immune signatures of pediatric AD and investigate the differences between pediatric and adult AD patients. Nine pediatric (6-16 years) and 12 adult (20-60 years) were enrolled. PBMCs were collected from AD patients and age- and sex-matched healthy controls (HCs). Transcriptomic profiles were analyzed using single-cell RNA sequencing, and the immune phenotypes of adult and pediatric AD were compared. Th2 gene expression was elevated in both adult and pediatric AD, while Th1, Th17, and Th22 gene expression was downregulated in pediatric AD but not in adults. Genes involved in JAK/STAT signaling pathway, which were upregulated in adult AD, were not significantly increased in pediatric AD. The CD6-activated leukocyte cell adhesion molecule (ALCAM) pathway was upregulated in pediatric AD compared to pediatric HCs, but not in adult AD. Pediatric AD reveals distinct immune signatures, including a lack of JAK/STAT pathway upregulation observed in adult AD and a unique activation of the CD6-ALCAM pathway. These findings highlight the importance of age-specific treatment strategies in AD patients.
与成人特应性皮炎(AD)相比,儿童特应性皮炎具有明显的临床特征,提示其独特的炎症特征可能影响疾病预后和治疗反应。我们旨在确定儿童AD的独特免疫特征,并研究儿童和成人AD患者之间的差异。招募了9名儿童(6 - 16岁)和12名成人(20 - 60岁)。从AD患者以及年龄和性别匹配的健康对照(HCs)中收集外周血单核细胞(PBMCs)。使用单细胞RNA测序分析转录组谱,并比较成人和儿童AD的免疫表型。Th2基因表达在成人和儿童AD中均升高,而Th1、Th17和Th22基因表达在儿童AD中下调,但在成人中未下调。参与JAK/STAT信号通路的基因在成人AD中上调,但在儿童AD中未显著增加。与儿童HCs相比,儿童AD中CD6激活的白细胞细胞粘附分子(ALCAM)途径上调,但在成人AD中未上调。儿童AD显示出独特的免疫特征,包括在成人AD中未观察到的JAK/STAT途径上调缺失以及CD6 - ALCAM途径的独特激活。这些发现突出了针对AD患者年龄特异性治疗策略的重要性。