Developing a Molecular Map of Atopic Dermatitis Across Ethnicity and Severity Subtypes.

项目摘要 阿尔茨海默病不同表型(即不同种族表型和不同表型)患者的治疗选择 疾病的严重性)不应该是偶然的，而应该由激活的不同来指导 免疫回路和相应的屏障改变。我们的主要假设是不同的AD 内型(基于种族和严重程度)在皮肤和血液中有不同的分子表型 这可能需要使用不同的治疗方法。我们第一个发现背后的次要假设 项目是阿尔茨海默病的离散亚型/内型存在于不同的种族人群中。我们的第一次 该项目旨在确定非洲和亚洲中到重度AD患者的皮肤和血液表型， 并确定它们是否与美国的AA和亚洲AD患者相似，这意味着全球非洲 和亚洲AD表型。我们第二个项目背后的子假说是严重的阿尔茨海默病 被认为是整个皮肤表面的一种全身性疾病，免疫激活延伸到非 皮损皮肤和循环细胞因子，而轻度疾病可能只反映局限性皮损皮肤 炎症而不累及全身。这可能解释了系统治疗的必要性和 重症患者仅用局部药物治疗皮损的不足。这项研究将定义一个 全身炎症的起始点，可能需要全身治疗。第二个项目的目标是 是定义与疾病严重程度(从轻度/局限性)相关的皮肤和血液生物标记物 通过严重/广泛的疾病)。这项研究将纳入18岁以上的成年AD患者和对照组。 将进行SCORAD、EASI、身体表面积(BSA)、NRS瘙痒和睡眠缺失评估。血样 对于CBC，血清(循环细胞因子和趋化因子，IgE和特异性IgE水平)和流式细胞术将 被画出来。将采集Pax RNA(用于基因表达)和PAX DNA(用于遗传分析)血液样本。 将进行4.5 mm皮损/LS和非皮损/NL穿孔活组织检查，以使用基因组进行皮肤特征分析 (RNAseq和qRT-PCR)和免疫组织化学方法。微生物组的TEWL和拭子将是 在活组织检查前在相同的位置进行。将进行外显子组测序以评估 每个种族/严重程度组的遗传血统。这是第一次提供系统生物学的研究。 阿尔茨海默病的方法，旨在制作一张跨越不同种族背景和 疾病严重亚组，可能确定专门针对 特定的种族背景或严重性。该提案将为基于AD的个性化治疗奠定基础 与种族有关的皮肤和血液生物标记物(屏障、免疫激活、微生物组、遗传风险等位基因) 和严重性，并将促进测试和开发创新的途径导向的治疗方法 对于不同的种族背景和不同的AD严重程度。

Project Summary Selection of therapeutics for patients with different AD phenotypes (i.e differing ethnic phenotypes and varying disease severity) should not be done by serendipity, but should be guided by differences in activation of immune circuits, and respective barrier alterations. Our overarching hypothesis is that different AD endotypes (based on ethnicity and severity) have different molecular phenotypes in skin and blood that may require use of different therapeutic approaches. The sub-hypothesis underlying our first project is that discrete subtypes/endotypes of AD exist within different ethnic populations. Our first project aims to define the skin and blood phenotypes of moderate-to-severe AD patients from Africa and Asia, and determine whether they are similar to those of AA and Asian AD patients in the US, implying global African and Asian AD phenotypes. The sub-hypothesis underlying our second project is that severe AD may be considered a systemic disease of the entire skin surface with immune activation extending to non- lesional skin and circulating cytokines, while mild disease may reflect only focal lesional skin inflammation without major systemic involvement. This may explain the need for systemic treatments and the inadequacy of treating only lesional skin with topical agents in severe patients. This study will define an onset point for systemic inflammation that may necessitate systemic treatments. The aim of the second project is to define the skin and blood biomarkers associated with increasing disease severity (from mild/limited through severe/extensive disease). The study will enroll adult AD patients and controls above 18 years old. SCORAD, EASI, body surface area (BSA), NRS pruritus and sleep loss assessments will be performed. Blood for CBC, serum (for circulating cytokines and chemokines, IgE and specific IgE levels), and flow cytometry, will be drawn. PAX RNA (for gene expression) and PAX DNA (for genetic analyses) blood samples will be taken. 4.5 mm lesional/LS and non-lesional/NL punch biopsies will be performed for skin profiling using genomic (RNAseq and qRT-PCR) and immunohistochemistry approaches. TEWL and swabs for microbiome will be performed from the same locations prior to biopsies. Exome sequencing will be performed to assess for genetic ancestry of each ethnicity/severity group. This is the first investigation that provides a system biology approach for AD, aiming to produce a molecular map of AD across its different ethnic backgrounds and disease severity sub-groups, which can possibly identify new therapeutics specifically geared towards a particular ethnic background, or severity. The proposal will set the stage for personalized therapy for AD based on skin and blood biomarkers (barrier, immune activation, microbiome, genetic risk alleles) related to ethnicity and severity, and will promote testing and development of innovative pathway-directed therapeutic approaches for the different ethnic backgrounds and varying AD severity.