首页> 外文期刊>Clinica chimica acta: International journal of clinical chemistry and applied molecular biology >Establishment of a protein biochip to detect serum IgG antibodies against IL-2 and soluble CD25 in hemophagocytic lymphohistiocytosis
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Establishment of a protein biochip to detect serum IgG antibodies against IL-2 and soluble CD25 in hemophagocytic lymphohistiocytosis

机译:建立蛋白生物芯片以检测血清IgG抗体对IL-2和可溶性CD25的血液活性淋巴管症

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BackgroundInterleukin-2 (IL-2) and soluble CD25 (sCD25) are among the most important cytokines and diagnostic biomarkers in hemophagocytic lymphohistiocytosis (HLH). Detecting serum level of IL-2 and sCD25 is valuable for making clinical diagnosis and treatment decision in HLH. MethodsSince tests showing serum IgG antibody against IL-2 or sCD25 have never been carried out, a new protein biochip, which was modified with cysteine and activated sophorolipid (Cys-SL), was developed. ResultsLimits of detection on the biochip were 78?pg/ml for IL-2 and 39?pg/ml for sCD25, respectively. The data showed that on-chip seroimmunological responses to IL-2 and sCD25 proteins were 20.8% and 83.1% and the seroprevalence of IL-2 and sCD25 IgG antibodies were 45.5% and 57.2%, respectively. Data collection for the seroprevalence of serum antigen-antibody complex of sCD25 was 68.8%. The new biochip model shared similar sensitivity and specificity to chemiluminescent immunoassay (CLIA) in its measuring capacity of serum sCD25. ConclusionsWe addressed and confirmed the involvement of serum IgG antibodies against IL-2 and sCD25 as well as Ag-Ab complex of sCD25 in HLH patients. Therefore, this biochip platform would offer a new technological substitution for clinical serological diagnosis of HLH.
机译:背景interlyukin-2(IL-2)和可溶性CD25(SCD25)是血糖淋巴管肾小球菌(HLH)中最重要的细胞因子和诊断生物标志物之一。检测血清IL-2和SCD25水平对于在HLH中进行临床诊断和治疗决策是有价值的。方法对从未进行过IL-2或SCD25的血清IgG抗体的试验,开发了一种用半胱氨酸和活化的Sophoripid(Cys-S1)改性的新蛋白质生物芯片。对生物芯片的检测结果分别为SCD25的IL-2和39〜Pg / ml为78〜pg / ml。该数据显示对IL-2和SCD25蛋白的片内血清轴理应答分别为20.8%和83.1%,IL-2和SCD25 IgG抗体的Seroprevaly分别为45.5%和57.2%。 SCD25的血清抗原抗体复合物的SEROPREVALING的数据收集为68.8%。新的Biochip模型在血清SCD25的测量能力中对化学发光免疫测定(CLIA)共享了类似的敏感性和特异性。结论我们已经解决并确认了血清IgG抗体对IL-2和SCD25以及SCD25中的AG-AB复合物的参与。因此,这种Biochip平台将为HLH的临床血清学诊断提供新的技术替代。

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