K. Hon, K. Tsang, J. Kung, T. Leung, C. Lam, C. Wong
{"title":"临床体征、葡萄球菌及特应性湿疹相关血清标志物","authors":"K. Hon, K. Tsang, J. Kung, T. Leung, C. Lam, C. Wong","doi":"10.3390/molecules22020291","DOIUrl":null,"url":null,"abstract":"Childhood eczema or atopic dermatitis (AD) is a distressing disease associated with pruritus, sleep disturbance, impaired quality of life and Staphylococcus aureus isolation. The pathophysiology of AD is complex and various seromarkers of immunity are involved. We investigated if anti-staphylococcal enterotoxin IgE (anti-SE), selected seromarkers of T regulatory (Treg), T helper (Th) and antigen-presenting cells (APC) are associated with clinical signs of disease severity and quality of life. Disease severity was assessed with the Scoring Atopic Dermatitis (SCORAD) index, and quality of life with the Children’s Dermatology Life Quality Index (CDLQI) in AD patients ≤18 years old. Concentrations of anti-staphylococcus enterotoxin A and B immunoglobulin E (anti-SEA and anti-SEB), selected Treg/Th/APC chemokines, skin hydration and transepidermal water loss (TEWL) were measured in these patients. Forty patients with AD [median (interquartile range) age of 13.1 (7.9) years) were recruited. Backward stepwise linear regression (controlling for age, personal allergic rhinitis and asthma, and other blood markers) showed the serum anti-SEB level was positively associated with S. aureus and S. epidermidis isolations, objective SCORAD, clinical signs and CDLQI. TNF-α (a Th1 cytokine) was positively associated with objective SCORAD (B = 4.935, p = 0.010), TGF-β (a Treg cytokine) negatively with disease extent (B = −0.015, p = 0.001), IL-18 (an APC cytokine) positively with disease extent (B = 0.438, p = 0.001) and with TEWL (B = 0.040, p = 0.010), and IL-23 (an APC cytokine) negatively with disease extent (B = −2.812, p = 0.006) and positively with pruritus (B = 0.387, p = 0.007). Conclusions: Blood levels of anti-SEB, Th1, Treg and APC cytokines are correlated with various clinical signs of AD. AD is a systemic immunologic disease involving Staphylococcus aureus, cellular, humoral, cytokine and chemokine pathophysiology.","PeriodicalId":19033,"journal":{"name":"Molecules : A Journal of Synthetic Chemistry and Natural Product Chemistry","volume":"24 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2017-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"16","resultStr":"{\"title\":\"Clinical Signs, Staphylococcus and Atopic Eczema-Related Seromarkers\",\"authors\":\"K. Hon, K. Tsang, J. Kung, T. Leung, C. Lam, C. Wong\",\"doi\":\"10.3390/molecules22020291\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Childhood eczema or atopic dermatitis (AD) is a distressing disease associated with pruritus, sleep disturbance, impaired quality of life and Staphylococcus aureus isolation. The pathophysiology of AD is complex and various seromarkers of immunity are involved. We investigated if anti-staphylococcal enterotoxin IgE (anti-SE), selected seromarkers of T regulatory (Treg), T helper (Th) and antigen-presenting cells (APC) are associated with clinical signs of disease severity and quality of life. Disease severity was assessed with the Scoring Atopic Dermatitis (SCORAD) index, and quality of life with the Children’s Dermatology Life Quality Index (CDLQI) in AD patients ≤18 years old. Concentrations of anti-staphylococcus enterotoxin A and B immunoglobulin E (anti-SEA and anti-SEB), selected Treg/Th/APC chemokines, skin hydration and transepidermal water loss (TEWL) were measured in these patients. Forty patients with AD [median (interquartile range) age of 13.1 (7.9) years) were recruited. Backward stepwise linear regression (controlling for age, personal allergic rhinitis and asthma, and other blood markers) showed the serum anti-SEB level was positively associated with S. aureus and S. epidermidis isolations, objective SCORAD, clinical signs and CDLQI. TNF-α (a Th1 cytokine) was positively associated with objective SCORAD (B = 4.935, p = 0.010), TGF-β (a Treg cytokine) negatively with disease extent (B = −0.015, p = 0.001), IL-18 (an APC cytokine) positively with disease extent (B = 0.438, p = 0.001) and with TEWL (B = 0.040, p = 0.010), and IL-23 (an APC cytokine) negatively with disease extent (B = −2.812, p = 0.006) and positively with pruritus (B = 0.387, p = 0.007). Conclusions: Blood levels of anti-SEB, Th1, Treg and APC cytokines are correlated with various clinical signs of AD. 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引用次数: 16
摘要
儿童湿疹或特应性皮炎(AD)是一种令人痛苦的疾病,与瘙痒、睡眠障碍、生活质量受损和金黄色葡萄球菌分离有关。阿尔茨海默病的病理生理复杂,涉及多种免疫血清标志物。我们研究了抗葡萄球菌肠毒素IgE(抗se)、T调节(Treg)、T辅助(Th)和抗原呈递细胞(APC)血清标记物是否与疾病严重程度和生活质量的临床体征相关。用评分特应性皮炎(SCORAD)指数评估疾病严重程度,用儿童皮肤病生活质量指数(CDLQI)评估≤18岁AD患者的生活质量。测定抗葡萄球菌肠毒素A和B免疫球蛋白E(抗sea和抗seb)浓度、选定的Treg/Th/APC趋化因子、皮肤水化和经皮失水(TEWL)。招募了40例AD患者[中位年龄(四分位数间距)为13.1(7.9)岁)。后向逐步线性回归(控制年龄、个人变应性鼻炎和哮喘等血液指标)显示,血清抗seb水平与金黄色葡萄球菌和表皮葡萄球菌分离、客观SCORAD、临床体征和CDLQI呈正相关。TNF-α (Th1细胞因子)与客观SCORAD呈正相关(B = 4.935, p = 0.010), TGF-β (Treg细胞因子)与疾病程度呈负相关(B = - 0.015, p = 0.001), IL-18 (APC细胞因子)与疾病程度呈正相关(B = 0.438, p = 0.001),与TEWL呈正相关(B = 0.040, p = 0.010), IL-23 (APC细胞因子)与疾病程度呈负相关(B = - 2.812, p = 0.006),与瘙痒呈正相关(B = 0.387, p = 0.007)。结论:血液中抗seb、Th1、Treg和APC细胞因子水平与AD的各种临床症状相关。AD是一种涉及金黄色葡萄球菌、细胞、体液、细胞因子和趋化因子病理生理的全身性免疫性疾病。
Clinical Signs, Staphylococcus and Atopic Eczema-Related Seromarkers
Childhood eczema or atopic dermatitis (AD) is a distressing disease associated with pruritus, sleep disturbance, impaired quality of life and Staphylococcus aureus isolation. The pathophysiology of AD is complex and various seromarkers of immunity are involved. We investigated if anti-staphylococcal enterotoxin IgE (anti-SE), selected seromarkers of T regulatory (Treg), T helper (Th) and antigen-presenting cells (APC) are associated with clinical signs of disease severity and quality of life. Disease severity was assessed with the Scoring Atopic Dermatitis (SCORAD) index, and quality of life with the Children’s Dermatology Life Quality Index (CDLQI) in AD patients ≤18 years old. Concentrations of anti-staphylococcus enterotoxin A and B immunoglobulin E (anti-SEA and anti-SEB), selected Treg/Th/APC chemokines, skin hydration and transepidermal water loss (TEWL) were measured in these patients. Forty patients with AD [median (interquartile range) age of 13.1 (7.9) years) were recruited. Backward stepwise linear regression (controlling for age, personal allergic rhinitis and asthma, and other blood markers) showed the serum anti-SEB level was positively associated with S. aureus and S. epidermidis isolations, objective SCORAD, clinical signs and CDLQI. TNF-α (a Th1 cytokine) was positively associated with objective SCORAD (B = 4.935, p = 0.010), TGF-β (a Treg cytokine) negatively with disease extent (B = −0.015, p = 0.001), IL-18 (an APC cytokine) positively with disease extent (B = 0.438, p = 0.001) and with TEWL (B = 0.040, p = 0.010), and IL-23 (an APC cytokine) negatively with disease extent (B = −2.812, p = 0.006) and positively with pruritus (B = 0.387, p = 0.007). Conclusions: Blood levels of anti-SEB, Th1, Treg and APC cytokines are correlated with various clinical signs of AD. AD is a systemic immunologic disease involving Staphylococcus aureus, cellular, humoral, cytokine and chemokine pathophysiology.