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The differential diagnostic model for asymptomatic HBV carriers established by MALDI-TOF-MS analysis

机译:MALDI-TOF-MS分析建立的无症状HBV载体的差分诊断模型

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Objectives: Hepatitis B virus can result in asymptomatic carrier (AsC) state or chronic inflammation of liver, which depends on the host immunity. The peptidomic profilings of HBV infection and immune responses are not thoroughly known for us. Methods: hi this study we established the diagnostic model and searched for the specific peptides which may influence various outcomes of HBV infection and could be used as clinical indicators for outcomes of HBV infection. Serum from 116 HBV infected (AsC and chronic hepatitis), 60 HBV-immunized and 70 normal subjects were treated with magnetic bead-based MB-WCX kits and analyzed by the Clinprot/ Matrix-Assisted Laser Desorption/ Ionization Time of Flight Mass Spectrometry (MALDI-TOF-MS) techniques. Purified plasma proteins were subjected to FT-ICR-MS analysis. Results: The serum peptide profiling had changed in asymptomatic carrier (AsC) and aggregately in chronic hepatitis. The specific model comprised of two peptides m/z 2882.89 and 4476.12 could distinguish HBV infected from healthy (HBV-immunized and normal) group and showed 95.5% of sensitivity and 95.4% of specificity by cross-validation analysis. 40/ 56 HBV infected and 43/ 50 healthy subjects could be correctly classified by the model. The area under the receiving operating curves of m/z 2882.89 and 4476.12 which were identified as fibrinogen beta chain (FBG) and nucleophosmin (NPM) respectively were both up to 0.88 when discriminating AsC from the healthy group. Conclusions: There was specific serum peptidomic profiling in the serum of HBV infected patients, and m/z 2882.89 and 4476.12 could be valuable follow-up and prognostic tools for HBV infection.
机译:目的:乙型肝炎病毒可导致无症状的载体(ASC)状态或肝脏慢性炎症,这取决于宿主免疫。 HBV感染和免疫应答的肽型分析对我们来说并不彻底。方法:在这项研究中,我们建立了诊断模型并搜索了可能影响HBV感染的各种结果的特定肽,可用作HBV感染结果的临床指标。血清来自116 HBV感染(ASC和慢性肝炎),60 HBV免疫和70个正常受试者用磁珠基Mb-Wcx试剂盒处理,并通过ClinProt /基质辅助激光解吸/电离时间来分析飞行质量光谱法( MALDI-TOF-MS)技术。对纯化的血浆蛋白质进行FT-ICR-MS分析。结果:血清肽分析已在无症状载体(ASC)中改变,慢性肝炎中的聚集在一起。由两种肽M / Z 2882.89和4476.12组成的具体模型可以区分HBV感染的HBV感染来自健康(HBV-免疫和正常)组,并且通过交叉验证分析显示95.5%的敏感性和95.4%的特异性。 40/56 HBV感染和43/50个健康受试者可以通过该模型正确归类。当鉴别来自健康组的ASC时,将鉴定为纤维蛋白原β链(FBG)和核磷脂(NPM)的接收操作曲线下的区域分别均多为0.88。结论:HBV感染患者的血清中存在特异性血清肽型分析,M / Z 2882.89和4476.12可能是HBV感染的有价值的后续和预后工具。

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