抗黄曲霉毒素B1单克隆抗体的制备研究

从影响融合率的2个主要因素探讨骨髓瘤细胞系Sp2/0细胞与黄曲霉毒素B_1免疫的脾细胞融合的最佳条件,使融合率达到100%.经筛选和克隆化,获得3株稳定分泌单克隆抗体的细胞株,分别命名为3B3、3H9、5G9.经过鉴定3株均为IgG_1亚类.其中3B3抗体与其他黄曲霉毒素几乎不发生交叉反应,腹水效价为1∶2×10~5,亲和力常数为3.1×10~7 L/mol,竞争性ELISA测出3B3抗体的最低反应浓度为0.05μg/L标准AFB_1样品的的回收率达96%.另外两株腹水抗体水平低,交叉反应强烈,腹水效价仅在1∶10~4数量级.     

白斑综合征病毒膜蛋白VP124参与病毒的感染

3种白斑综合征病毒膜蛋白(VP39、VP124和VP187)各自特异性抗血清用于体外中和试验,研究它们是否参与病毒的感染,进一步用定量PCR检测中和试验中病毒的感染情况.结果表明,WSSV的感染能够被抗VP124抗体中和,VP124在病毒的感染中有起作用.     

矽肺病人的免疫状态

本文检查了矽肺病人的多种免疫状态,发现患者同围血中T细胞百分率平均值比对照组显著降低,而B细胞百分率呈有意义增高;血清蛋白、r、α_1、α_2球蛋白有随病程进展而增高趋势;血清免疫球蛋白IgG和IgA含量的增高亦与病程相一致,至Ⅱ期矽肺二者含量增高显著,但IgM含量未见明显变化,仅在矽肺合并结核组,IgG、IgA、和IgM含量呈明显增高;患者组类风湿因子(RF)和抗核抗体(ANA)合并阳性率(24.5％)比接尘组(13.3％)为高;血中循环免疫复合物(CIC)阳性检出率较高,但Ⅰ期矽肺组与对照组相比,未呈统计学差别;患者血中总补体(CH_(50))和C_8含量未见明显变化。根据患者的T细胞检出率降低,B细胞增高、体液免疫结果与细胞免疫相一致,均和病程进展而呈现规律性变化,以及自身抗体增高等免疫现象,似与自身免疲性疾病有类同之处。随着杂交瘤技术的广泛应用,联系近年国外关于石棉肺免疫学研究,对T细胞亚群变化进行了讨论,这方面的深入研究,对阐明矽肺发病机理是有意义的。对矽肺免疫的进一步研究,从实验设计上也提出了有益的建议。     

新型仿生亲和介质纯化工艺生产效率分析

抗体的捕获层析的成本在整个抗体纯化工艺中占有相当的比例.分析比较了新型小分子仿生亲和介质和常规蛋白A的动态载量、循环使用次数和线性流速等参数,并计算了相应的生产效率,发现新型小分子仿生亲和介质最高生产效率能达到蛋白A亲和层析介质最高生产效率的3⁶.9倍.     

Identification of a New Member of the Ep-CAM (17-1A) Tumor-Associated Antigen Family

IntroductionThe tumor- associated antigen,epithelial celladhesion molecule (Ep- CAM ) ,defined by themurine m Ab1 7- 1 A,is expressed on the surface ofvarious types of normal and malignant humanepithelial tissues,which makes it an attractivetarget for immunotherapy[15] . Adjuvantimmunotherapy treatment with the m Ab 1 7- 1 Asuccessfully reduced the 5 - year mortality andrecurrence rate among colorectal cancer patientswith minimal residual disease[6 ] .　Studies on Ep- CAM,alias 1 7- 1 A a…     

龙虎山猕猴(Macaca mulatta)麻疹病毒感染的探讨

采用HI(血凝抑制试验)法,比较在不同生境中,龙虎山猕猴麻疹病毒抗体阳性率的差异:小群关养组的阳性率为90.9%;半野生猴组阳性率为28.3%;野生猴组阳性率为2.4%。不同性别及不同年龄猴麻疹病毒抗体阳性率没有显著性差异(P>0.01)。半野生猴组阳性率逐年递增。对建立无麻疹、B病毒等病毒感染繁殖种群提出初步意见。     

蛋白激酶C单克隆抗体的制备

应用杂交瘤技术制备了蛋白激酶C(PKC)的单克隆抗体,用蛋白A-Sepharose-CL4B协同沉淀复合物分析单抗识别的蛋白,分子质量与PKC相同。采用该抗体对正常和转化的C_3H_(10) T_(1/2)细胞进行免疫荧光观察,发现它们的PKC含量明显不同。但荧光分布都主要集中在细胞质和细胞膜部分。     

Aberrant DNA methylation patterns in cultured mouse embryos

Mouse early embryos undergo genome-wide demethylation and remethylation events during pre-implantation development. Abnormal methylation reprogramming is thought to be associated with development arrest. Using immunofluorescence staining with an antibody against 5-methylcytosine (MeC), we examined the genome methylation patterns of mouse embryos cultured in vitro. The results did not show the difference in staining patterns between development-blocked two-cell embryos that cultured in vitro and the two-cell embryos that were freshly collected from the donor mice. But in vitro-arrested morulae displayed a strong positive staining when compared to the morulae freshly collected from the donor mice. At the blastocyst stage, although most embryos showed the expected methylation patterns, with highly stained inner cell mass (ICM) and weekly stained trophectoderm (TE), a proportion of embryos were dimly stained in both ICM and TE. These results indicated that the methylation profile of the embryos could be changed by culturing in vitro when the embryos were in the transition from morulae to blastocyst.     

Carbohydrate interference of complement-dependent cell lysis

Summary The antibody-mediated cytotoxicity of three autoreactive sera, an allogeneic hyperimmune serum and a xenogeneic hyperimmune serum was abrogated by the presence of either glucosamine, galactosamine, lactulose or lactose. This inhibition could be overcome in a dose-dependent fashion by increasing the amount of complement in the cytotoxicity assay, but not by increasing the amount of antibody. Furthermore, the inhibition was specific for these sugars in that isomers and N-acetylated derivatives were not inhibitory. The results suggest that these sugars directly blocked events of the complement cascade.