目的:探究单纯疱疹病毒(HSV)感染后脑脊液(CSF)中S100B、Cys-C、MMP-9水平对自身免疫性脑炎(AE)的预测价值。方法:选取2016年1月至2021年3月河北中石油中心医院收治的200例HSV感染患者为研究对象,根据是否继发AE分为研究组(继发AE,35例...目的:探究单纯疱疹病毒(HSV)感染后脑脊液(CSF)中S100B、Cys-C、MMP-9水平对自身免疫性脑炎(AE)的预测价值。方法:选取2016年1月至2021年3月河北中石油中心医院收治的200例HSV感染患者为研究对象,根据是否继发AE分为研究组(继发AE,35例)和对照组(未继发AE,165例)。多因素Logistic回归分析HSV感染患者继发AE的独立影响因素。Spearman法分析脑脊液中Cys-C、MMP-9与S100B水平的相关性。受试者工作特征(ROC)曲线分析S100B、Cys-C、MMP-9对AE的预测价值。构建风险预测模型并进行评价。结果:多因素Logistic回归分析显示,MRI异常、脑脊液S100B、MMP-9升高、EEG异常是HSV感染患者继发AE的独立危险因素,脑脊液Cys-C是其保护因素(P<0.05)。Spearman分析显示,HSV感染患者Cys-C浓度与S100B水平呈负相关(r=-0.83,P<0.05),MMP-9浓度与S100B水平呈正相关(r=0.88,P<0.05)。构建的联合预测因子pre1诊断HSV患者继发AE的AUC明显大于S100B、Cys-C、MMP-9单独预测的AUC(0.876 vs 0.827、0.787、0.750)。构建的风险预测模型具有良好的区分度和一致性。结论:脑脊液中S100B、Cys-C、MMP-9水平均可对HSV感染患者诱发AE的可能性进行有效预测,且三项指标联合预测价值最大,其次是S100B蛋白、Cys-C、MMP-9。展开更多
目的探讨S100b联合CRP在诊断早产儿脑损伤(Brain injury in premature infants,BIPI)中的临床效能。方法选择2022年1月—2024年1月于本院儿科确诊的125例BIPI患儿作为BIPI组,另选择同期收治的85例非BIPI早产儿作为对照组。根据BIPI患儿...目的探讨S100b联合CRP在诊断早产儿脑损伤(Brain injury in premature infants,BIPI)中的临床效能。方法选择2022年1月—2024年1月于本院儿科确诊的125例BIPI患儿作为BIPI组,另选择同期收治的85例非BIPI早产儿作为对照组。根据BIPI患儿病情严重程度分为轻度BIPI组和重度BIPI组两组亚组。收集所有研究对象的临床资料并检测血清中S100b联合CRP表达水平。Logistic回归分析发生BIPI的危险因素,S100b联合CRP在诊断BIPI的临床效能采用ROC曲线分析。结果对照组、轻度BIPI组和重度BIPI组三组间S100b、CRP表达水平存在统计学差异(P<0.05)。与对照组相比,轻度和重度BIPI组S100b、CRP表达水平均明显升高(P<0.05);与轻度BIPI组相比,重度BIPI组S100b、CRP表达水平均明显升高(P<0.05)。与对照组相比,宫内窘迫、出生后窒息、有创机械通气、新生儿呼吸窘迫综合征发生率及血清中S100b、CRP表达水平在BIPI组中明显升高(P<0.05)。Logistic回归分析结果显示,有创机械通气(OR=1.432)、新生儿呼吸窘迫综合征(OR=2.543)、S100b(OR=3.782)和CRP表达(OR=3.449)是发生BIPI的危险因素。S100b及CRP在诊断BIPI的曲线下面积分别为0.895和0.812,S100b联合CRP在诊断BIPI的曲线下面积为0.931,诊断敏感度和特异度分别为97.43%和92.25%。结论BIPI患儿外周血中S100b和CRP表达水平显著升高,S100b联合CRP在诊断BIPI中具有显著的临床价值。展开更多
AIM: To investigate the biological function of complete S protein and to look for proteins interacting with complete S protein in hepatocytes.METHODS: We constructed bait plasmid expressing complete S protein of HBV b...AIM: To investigate the biological function of complete S protein and to look for proteins interacting with complete S protein in hepatocytes.METHODS: We constructed bait plasmid expressing complete S protein of HBV by cloning the gene of complete S protein into pGBKT7, then the recombinant plasmid DNA was transformed into yeast AH109 (a type). The transformed yeast AH109 was mated with yeast Y187 (α type) containing liver cDNA library plasmid in 2xYPDA medium. Diploid yeast was plated on synthetic dropout nutrient medium (SD/Trp-Leu-His-Ade) containing X-α-gal for selection and screening. After extracting and sequencing of plasmids from positive (blue) colonies, we underwent sequence analysis by bioinformatics.RESULTS: Nineteen colonies were selected and sequenced.Among them, five colonies were Homo sapiens solute carrier family 25, member 23 (SLC25A23), one was Homo sapiens calreticulin, one was human serum albumin (ALB)gene, one was Homo sapiens metallothionein 2A, two were Homo sapiens betaine-homocysteine methyltransferase,three were Homo sapiensNa+ and H+ coupled amino acid transport system N, one was Homo sapiens CD81 antigen (target of anti-proliferative antibody 1) (CD81), three were Homo sapiens diazepam binding inhibitor, two colonies were new genes with unknown function.CONCLUSION: The yeast-two hybrid system is an effective method for identifying hepatocyte proteins interacting with complete S protein of HBV. The complete S protein may bind to different proteins i.e., its multiple functions in vivo.展开更多
文摘目的:探究单纯疱疹病毒(HSV)感染后脑脊液(CSF)中S100B、Cys-C、MMP-9水平对自身免疫性脑炎(AE)的预测价值。方法:选取2016年1月至2021年3月河北中石油中心医院收治的200例HSV感染患者为研究对象,根据是否继发AE分为研究组(继发AE,35例)和对照组(未继发AE,165例)。多因素Logistic回归分析HSV感染患者继发AE的独立影响因素。Spearman法分析脑脊液中Cys-C、MMP-9与S100B水平的相关性。受试者工作特征(ROC)曲线分析S100B、Cys-C、MMP-9对AE的预测价值。构建风险预测模型并进行评价。结果:多因素Logistic回归分析显示,MRI异常、脑脊液S100B、MMP-9升高、EEG异常是HSV感染患者继发AE的独立危险因素,脑脊液Cys-C是其保护因素(P<0.05)。Spearman分析显示,HSV感染患者Cys-C浓度与S100B水平呈负相关(r=-0.83,P<0.05),MMP-9浓度与S100B水平呈正相关(r=0.88,P<0.05)。构建的联合预测因子pre1诊断HSV患者继发AE的AUC明显大于S100B、Cys-C、MMP-9单独预测的AUC(0.876 vs 0.827、0.787、0.750)。构建的风险预测模型具有良好的区分度和一致性。结论:脑脊液中S100B、Cys-C、MMP-9水平均可对HSV感染患者诱发AE的可能性进行有效预测,且三项指标联合预测价值最大,其次是S100B蛋白、Cys-C、MMP-9。
文摘目的探讨S100b联合CRP在诊断早产儿脑损伤(Brain injury in premature infants,BIPI)中的临床效能。方法选择2022年1月—2024年1月于本院儿科确诊的125例BIPI患儿作为BIPI组,另选择同期收治的85例非BIPI早产儿作为对照组。根据BIPI患儿病情严重程度分为轻度BIPI组和重度BIPI组两组亚组。收集所有研究对象的临床资料并检测血清中S100b联合CRP表达水平。Logistic回归分析发生BIPI的危险因素,S100b联合CRP在诊断BIPI的临床效能采用ROC曲线分析。结果对照组、轻度BIPI组和重度BIPI组三组间S100b、CRP表达水平存在统计学差异(P<0.05)。与对照组相比,轻度和重度BIPI组S100b、CRP表达水平均明显升高(P<0.05);与轻度BIPI组相比,重度BIPI组S100b、CRP表达水平均明显升高(P<0.05)。与对照组相比,宫内窘迫、出生后窒息、有创机械通气、新生儿呼吸窘迫综合征发生率及血清中S100b、CRP表达水平在BIPI组中明显升高(P<0.05)。Logistic回归分析结果显示,有创机械通气(OR=1.432)、新生儿呼吸窘迫综合征(OR=2.543)、S100b(OR=3.782)和CRP表达(OR=3.449)是发生BIPI的危险因素。S100b及CRP在诊断BIPI的曲线下面积分别为0.895和0.812,S100b联合CRP在诊断BIPI的曲线下面积为0.931,诊断敏感度和特异度分别为97.43%和92.25%。结论BIPI患儿外周血中S100b和CRP表达水平显著升高,S100b联合CRP在诊断BIPI中具有显著的临床价值。
基金Supported by the National Natural Science Foundation of China, No. C03011402, No. C30070690the Science and Technique Foundation of PLA during the 9th Five-year plan period, No. 98D063 the Launching Foundation for Students Studying Abroad of PLA, No. 98H038 the Youth Science and Technique Foundation of PLA during the 10lh Five-year plan period, No. 01Q138and the Science & Technique Foundation of PLA during the 10th Five-year plan period, No. 01MB135
文摘AIM: To investigate the biological function of complete S protein and to look for proteins interacting with complete S protein in hepatocytes.METHODS: We constructed bait plasmid expressing complete S protein of HBV by cloning the gene of complete S protein into pGBKT7, then the recombinant plasmid DNA was transformed into yeast AH109 (a type). The transformed yeast AH109 was mated with yeast Y187 (α type) containing liver cDNA library plasmid in 2xYPDA medium. Diploid yeast was plated on synthetic dropout nutrient medium (SD/Trp-Leu-His-Ade) containing X-α-gal for selection and screening. After extracting and sequencing of plasmids from positive (blue) colonies, we underwent sequence analysis by bioinformatics.RESULTS: Nineteen colonies were selected and sequenced.Among them, five colonies were Homo sapiens solute carrier family 25, member 23 (SLC25A23), one was Homo sapiens calreticulin, one was human serum albumin (ALB)gene, one was Homo sapiens metallothionein 2A, two were Homo sapiens betaine-homocysteine methyltransferase,three were Homo sapiensNa+ and H+ coupled amino acid transport system N, one was Homo sapiens CD81 antigen (target of anti-proliferative antibody 1) (CD81), three were Homo sapiens diazepam binding inhibitor, two colonies were new genes with unknown function.CONCLUSION: The yeast-two hybrid system is an effective method for identifying hepatocyte proteins interacting with complete S protein of HBV. The complete S protein may bind to different proteins i.e., its multiple functions in vivo.