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舌下免疫疗法降低变应性鼻炎患儿白细胞介素-33 的表达。

Sublingual Immunotherapy Decreases Expression of Interleukin-33 in Children with Allergic Rhinitis.

机构信息

Department of Otolaryngology, Dongguan Women and Children's Hospital, No 99. Zhenxing Road, Dongguan, 523120, China.

出版信息

Indian J Pediatr. 2018 Oct;85(10):872-876. doi: 10.1007/s12098-018-2703-3. Epub 2018 May 23.

Abstract

OBJECTIVES

To identify the expression of IL-33 during SLIT (Sublingual immunotherapy) in AR (Allergic rhinitis) children.

METHODS

Thirty children received house dust mite (HDM) allergen extract for SLIT and thirty children received placebo in this study. Serum and nasal lavage samples of cases and controls were collected at different time points during SLIT. Interleukin (IL)-33 and other cytokines were estimated in these samples by enzyme-linked immuno sorbent assay (ELISA). Peripheral blood mononuclear cells (PBMC) were prepared and stimulated with rhIL-33 (with or without other stimulators) at different time points during SLIT.

RESULTS

The present results showed that both serum and nasal lavage of IL-33 levels decreased significantly after 12 mo treatment and this trend maintained at least until 24 mo. The decreased nasal IL-33 level was positively correlated to local Th2 cytokines and increased IL-10 expression at 2 y post SLIT treatment. In vitro experiments showed that IL-33 promotes IL-4 and IL-5 and inhibits IL-10 expression by peripheral blood mononuclear cells (PBMCs) in AR.

CONCLUSIONS

Decreased IL-33 expression during SLIT may contribute to low Th2 response and enhanced Regulatory T cell cytokines expression. Thus, IL-33 maybe an important predictor during SLIT.

摘要

目的

鉴定 SLIT(舌下免疫疗法)过程中白细胞介素-33(IL-33)在变应性鼻炎(AR)儿童中的表达。

方法

本研究中,30 名儿童接受屋尘螨(HDM)过敏原提取物进行 SLIT,30 名儿童接受安慰剂。在 SLIT 过程中的不同时间点收集病例和对照的血清和鼻洗液样本。通过酶联免疫吸附试验(ELISA)在这些样本中估计白细胞介素(IL)-33和其他细胞因子。在 SLIT 过程中的不同时间点,用 rhIL-33(有或没有其他刺激物)制备外周血单核细胞(PBMC)并进行刺激。

结果

本研究结果表明,血清和鼻洗液中的 IL-33 水平在治疗 12 个月后显著降低,这种趋势至少持续到 24 个月。鼻内 IL-33 水平的降低与局部 Th2 细胞因子呈正相关,并且在 SLIT 治疗后 2 年增加了 IL-10 的表达。体外实验表明,IL-33 通过外周血单核细胞(PBMC)促进 IL-4 和 IL-5 的表达,抑制 IL-10 的表达。

结论

SLIT 过程中 IL-33 表达的降低可能导致 Th2 反应降低和调节性 T 细胞细胞因子表达增强。因此,IL-33 可能是 SLIT 期间的一个重要预测指标。

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