Department of Clinical and Experimental Medicine, Division of Pediatrics, Linköping University, Linköping, Sweden.
Clin Exp Allergy. 2011 Dec;41(12):1729-39. doi: 10.1111/j.1365-2222.2011.03827.x. Epub 2011 Aug 1.
Analyses of circulating chemokines offer novel tools to investigate the T helper (Th)1/Th2 imbalance in allergic disease in vivo.
To relate circulating Th1- and Th2-associated chemokines in infancy to allergic disease, sensitization and probiotic supplementation.
Circulating levels of Th1-associated CXC-chemokine ligand (CXCL)9, CXCL10 and CXCL11 and Th2-associated CC-chemokine ligand (CCL)17 and CCL22 were assessed with Luminex and CCL18 with enzyme-linked immunosorbent assay at birth (n=109), 6 (n=104), 12 (n=116) and 24 months (n=123) in 161 infants completing a double-blind placebo-controlled allergy prevention trial with Lactobacillus reuteri during the last month of gestation and through the first year of life. The infants were followed regarding the development of allergic disease and sensitization until 2 years of age.
The Th2-associated chemokines CCL17 and CCL22 were the highest at birth and then decreased, whereas CCL18 and the Th1-associated chemokines increased with age. High Th2-associated chemokine levels were observed in children developing allergic disease. Sensitization was preceded by elevated levels of the Th2-associated CCL22 and reduced levels of the Th1-associated CXCL11 already at birth. The Th2-associated CCL17 was also elevated at birth in infants developing recurrent wheeze. A high Th2/Th1 ratio (CCL22/CXCL10) at birth associated with both sensitization and eczema development. The presence of L. reuteri in stool in the first week of life was associated with low CCL17 and CCL22 and high CXCL11 levels at 6 months of age. High Th1-associated chemokine levels were associated with day-care.
Allergic disease and sensitization in infancy was associated with low circulating Th1- and high Th2-associated chemokine levels already from birth. Circulating chemokines are useful for investigating the Th1/Th2 imbalance in allergic disease in vivo. Elucidation of the role of chemokines in allergic diseases may lead to future treatments (ClinicalTrials.gov NCT01285830).
分析循环趋化因子可提供新的工具,以研究体内变态反应性疾病中的辅助性 T 细胞(Th)1/Th2 失衡。
将婴儿期循环 Th1 和 Th2 相关趋化因子与变态反应性疾病、致敏和益生菌补充相关联。
采用 Luminex 法检测出生时(n=109)、6 个月(n=104)、12 个月(n=116)和 24 个月(n=123)时循环 Th1 相关趋化因子 CXC 配体(CXCL)9、CXCL10 和 CXCL11 及 Th2 相关趋化因子 CC 配体(CCL)17 和 CCL22 的水平,采用酶联免疫吸附法检测 CCL18 的水平。161 例婴儿完成了一项双盲安慰剂对照的预防过敏试验,在妊娠最后 1 个月和婴儿出生后第 1 年期间补充罗伊氏乳杆菌,直至 2 岁时对其进行变态反应性疾病和致敏情况的随访。
Th2 相关趋化因子 CCL17 和 CCL22 在出生时水平最高,随后下降,而 CCL18 和 Th1 相关趋化因子则随年龄增长而增加。发生变态反应性疾病的儿童 Th2 相关趋化因子水平较高。致敏前,Th2 相关趋化因子 CCL22 水平升高,Th1 相关趋化因子 CXCL11 水平降低,这一现象在出生时就已出现。出生时 Th2 相关趋化因子 CCL17 水平升高的婴儿也容易反复喘息。出生时 Th2/Th1 比值(CCL22/CXCL10)较高与致敏和湿疹的发生有关。出生后第 1 周粪便中存在罗伊氏乳杆菌与 6 个月时 CCL17 和 CCL22 水平较低、CXCL11 水平较高有关。高水平 Th1 相关趋化因子与日托有关。
婴儿期变态反应性疾病和致敏与出生时循环 Th1 相关趋化因子水平降低和 Th2 相关趋化因子水平升高有关。循环趋化因子可用于研究体内变态反应性疾病中 Th1/Th2 失衡。阐明趋化因子在变态反应性疾病中的作用可能为未来的治疗方法提供依据(ClinicalTrials.gov NCT01285830)。