对苯二胺致敏和多致敏:TNF-α、CXCL11和免疫调节基因多态性。

IF 1.3
Jin Ju Lee, Heera Lee, Ji Yeon Byun, You Won Choi, Joo Young Roh, Hae Young Choi
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引用次数: 0

摘要

背景:对苯二胺(PPD)是一种主要的染发剂过敏原,通常预示着更广泛的接触性过敏风险,但PPD致敏、多致敏(PS)与宿主遗传之间的关系仍未得到充分研究。目的:量化韩国斑贴试验患者PPD致敏与PS之间的关系,并探讨选定免疫调节基因的单核苷酸多态性(snp)是否调节这种关系。方法:我们回顾性分析了647例使用韩国标准系列贴片试验的韩国患者。PS定义为对≥3个不相关过敏原有反应性;镍、钴或铬酸盐同时呈阳性被算作一个事件。通过多变量逻辑回归确定PPD致敏性的独立预测因子,并通过热图可视化过敏原网络。对17例患者进行肿瘤坏死因子- α、CXCL11、白细胞介素(IL)-10、IL-16和STAT6的snp基因分型。结果:38例患者(5.9%)确认PPD致敏,且与PS独立相关(校正优势比[OR], 2.72; 95%可信区间,1.11-6.67)。其他化学预测因子为氯化汞铵(OR, 3.68; p=0.018)和香料混合I (OR, 3.18; p=0.013)。热图显示,在PPD阳性,特别是PS阳性亚群中,密集的防腐剂和橡胶过敏原聚集。探索性基因分型显示,PPD+/PS+患者的CXCL11变异频率(85.7%)与预期人群频率(东亚约50%)相比存在数值差异,尽管样本量小(n=17)排除了统计学意义检验。结论:PPD致敏可识别出PS风险增加以及对汞化合物和香味相关物质的反应性增加的患者。初步的遗传观察需要在更大规模的研究中进行验证,以确定潜在的免疫遗传学贡献。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Para-Phenylenediamine Sensitization and Polysensitization: TNF-α, CXCL11, and Immune-Regulatory Gene Polymorphisms.

Para-Phenylenediamine Sensitization and Polysensitization: TNF-α, CXCL11, and Immune-Regulatory Gene Polymorphisms.

Para-Phenylenediamine Sensitization and Polysensitization: TNF-α, CXCL11, and Immune-Regulatory Gene Polymorphisms.

Para-Phenylenediamine Sensitization and Polysensitization: TNF-α, CXCL11, and Immune-Regulatory Gene Polymorphisms.

Background: Para-phenylenediamine (PPD) is a major hair dye allergen and often heralds broader contact allergy risk, yet the links among PPD sensitization, polysensitization (PS) and host genetics remain understudied.

Objective: To quantify the association between PPD sensitization and PS in Korean patch test patients and to explore whether single nucleotide polymorphisms (SNPs) in selected immunoregulatory genes modulate this relationship.

Methods: We retrospectively analysed 647 Korean patients patch tested with the Korean Standard Series. PS was defined as reactivity to ≥3 unrelated allergens; simultaneous positives to nickel, cobalt or chromate were counted as one event. Independent predictors of PPD sensitization were determined by multivariable logistic regression, and allergen networks were visualised with heatmaps. Seventeen patients were genotyped for SNPs in tumor necrosis factor-alpha, CXCL11, interleukin (IL)-10, IL-16 and STAT6.

Results: PPD sensitization was confirmed in 38 patients (5.9%) and remained independently associated with PS (adjusted odds ratio [OR], 2.72; 95% confidence interval, 1.11-6.67). Additional chemical predictors were mercury ammonium chloride (OR, 3.68; p=0.018) and fragrance mix I (OR, 3.18; p=0.013). Heatmaps revealed dense preservative and rubber allergen clusters in PPD positive and particularly PS positive subsets. Exploratory genotyping showed numerical differences in CXCL11 variant frequency in PPD+/PS+ patients (85.7%) compared to expected population frequencies (about 50% in East Asians), though the small sample size (n=17) precluded statistical significance testing.

Conclusion: PPD sensitization identifies patients at increased risk for PS and reactivity to mercury compounds and fragrance-related substances. Preliminary genetic observations require validation in larger studies to determine potential immunogenetic contributions.

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