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首页> 外文期刊>Clinical and experimental allergy : >Recognition of iodixanol by dendritic cells increases the cellular response in delayed allergic reactions to contrast media.
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Recognition of iodixanol by dendritic cells increases the cellular response in delayed allergic reactions to contrast media.

机译:树突状细胞对碘克沙醇的识别增加了对造影剂的延迟过敏反应中的细胞反应。

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BACKGROUND: Delayed reactions to iodine contrast media (CM) account for 1-3% of patients with adverse reactions to iodine CM. The cellular and molecular mechanisms of these reactions remain poorly documented. Although most of these reactions are T cell mediated, the involvement of dendritic cells (DC) has not been investigated sufficiently. OBJECTIVE: To determine whether the T cell response to iodixanol requires DC as antigen-presenting cell and, more particularly, to evaluate the changes induced by iodixanol on DC maturation and in vitro production of cytokines after drug stimulation in patients with maculopapular exanthema. METHODS: Peripheral blood lymphocytes, immature monocyte-derived DC (imDC) and skin biopsies were obtained from patients with delayed reactions to iodixanol and tolerant subjects. We studied the consequences of the interaction between DC, lymphocytes and iodixanol by phenotype analysis, proliferation and cytokine production. RESULTS: A T-cell-mediated reaction was evidenced in patient biopsies, with a lymphocyte-rich, peri-vascular infiltrate. Iodixanol induced maturation of imDC from patients but not from controls, with expression of the co-stimulatory markers CD83, CD86 and CD40 and an increase in mean fluorescence intensity of CD80, CD86 and HLA-DR. In the absence of DC, positive cell proliferation to iodixanol was detected in only one patient while the addition of DC produced a positive test in five of the six patients. Similarly, the increase in cytokines (IFN-gamma, IL-2, IL-6, IL-1b and TNF-alpha) was higher when imDC were introduced into the culture together with the culprit drug. CONCLUSION AND CLINICAL RELEVANCE: These results provide evidence for a DC-mediated mechanism in delayed allergic reactions to CM, influencing T cell proliferation and cytokine production. These new insights will be helpful for designing immunotherapeutic strategies and in vitro diagnostic tests of CM-delayed reactions.
机译:背景:对碘造影剂(CM)的延迟反应占对碘CM不良反应的患者的1-3%。这些反应的细胞和分子机制仍然文献很少。尽管这些反应大多数是T细胞介导的,但尚未充分研究树突状细胞(DC)的参与。目的:确定对碘克沙醇的T细胞应答是否需要DC作为抗原呈递细胞,更具体地说,评估碘克沙醇对斑丘状皮疹患者药物刺激后DC成熟和体外细胞因子产生的变化。方法:从对碘克沙醇和耐受对象延迟反应的患者中获得外周血淋巴细胞,未成熟单核细胞衍生的DC(imDC)和皮肤活检。我们通过表型分析,增殖和细胞因子产生研究了DC,淋巴细胞和碘克沙醇之间相互作用的结果。结果:在患者的活组织检查中证实了T细胞介导的反应,其中淋巴细胞丰富,血管周围浸润。碘克沙醇诱导了患者的imDC成熟,但未引起对照的共刺激标记CD83,CD86和CD40的表达,以及CD80,CD86和HLA-DR的平均荧光强度增加。在没有DC的情况下,仅一名患者检测到碘克沙醇的阳性细胞增殖,而添加DC在六名患者中的五名中产生阳性测试。同样,当将imDC与罪魁祸首药物一起引入培养物中时,细胞因子(IFN-γ,IL-2,IL-6,IL-1b和TNF-α)的增加更高。结论和临床意义:这些结果提供了DC介导的延迟对CM的过敏反应,影响T细胞增殖和细胞因子产生的机制的证据。这些新见解将有助于设计CM延迟反应的免疫治疗策略和体外诊断测试。

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