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患特应性疾病低风险和高风险新生儿脐带血单个核细胞的共刺激分子表达及细胞因子谱

Costimulatory molecules expression and cytokine profiles of cord blood mononuclear cells in newborns with low and high risk of developing atopic diseases.

作者信息

Yang Y H, Chen M C, Tsai M J, Lin Y T, Chiang B L

机构信息

Department of Pediatrics, National Taiwan University Hospital, Taipei, ROC.

出版信息

J Microbiol Immunol Infect. 2000 Sep;33(3):159-64.

Abstract

This study sought to determine predictors of atopic diseases in newborns. We evaluated the levels of expression of costimulatory molecules (CD80 and CD86) and the production of cytokines [interleukin (IL)-12, interferon (IFN)-gamma, IL-4, IL-10] in the cord blood of mononuclear cells in high risk newborns (n = 17), and compared them with those in low risk newborns (n = 25). Fluorescence-activated cell sorter (FACScan) analysis was performed to determine the expressions of CD80 and CD86 on activated B cells and monocytes of both groups. The levels of IL-10, IL-12p40 and IL-12p70 in the supernatant were assayed by enzyme-linked immunosorbent assay (ELISA), and also the mRNA levels by reverse transcription-polymerase chain reaction (RT-PCR). Intracellular staining of IL-4 and IFN-gamma in stimulated mononuclear cells was also performed as well. The expressions of CD80 and CD86 on B cells showed no significant difference between the high and low risk group. There was greater expression of CD86 on the monocytes of low risk newborns as compared to high risk newborns (p < 0.05). When B cells and monocytes isolated from the cord blood of both groups were stimulated with mitogens, the production of IL-10, IL-12p40, and IL-12p70 in the supernatants was not significantly different. The expressions of mRNA of IL-10, IL-12p35, and IL-12p40, and the intracellular staining of IL-4 and IFN-gamma in stimulated mononuclear cells were not significantly different between the two groups. These findings suggested that cytokine profiles in the cord blood cannot predict the development of atopic diseases. Determination of whether preferential expression of costimulatory molecules is of predictive value or not will require further study.

摘要

本研究旨在确定新生儿特应性疾病的预测因素。我们评估了高危新生儿(n = 17)单核细胞脐带血中共刺激分子(CD80和CD86)的表达水平以及细胞因子[白细胞介素(IL)-12、干扰素(IFN)-γ、IL-4、IL-10]的产生,并将其与低危新生儿(n = 25)进行比较。采用荧光激活细胞分选仪(FACScan)分析来确定两组活化B细胞和单核细胞上CD80和CD86的表达。通过酶联免疫吸附测定(ELISA)检测上清液中IL-10、IL-12p40和IL-12p70的水平,同时通过逆转录-聚合酶链反应(RT-PCR)检测mRNA水平。还对刺激的单核细胞中的IL-4和IFN-γ进行了细胞内染色。高危组和低危组B细胞上CD80和CD86的表达无显著差异。与高危新生儿相比,低危新生儿单核细胞上CD86的表达更高(p < 0.05)。当用丝裂原刺激两组脐带血分离的B细胞和单核细胞时,上清液中IL-10、IL-12p40和IL-12p70的产生无显著差异。两组刺激的单核细胞中IL-10、IL-12p35和IL-12p40的mRNA表达以及IL-4和IFN-γ的细胞内染色无显著差异。这些发现表明,脐带血中的细胞因子谱不能预测特应性疾病的发展。共刺激分子的优先表达是否具有预测价值还需要进一步研究。

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