未免疫的

It was found that the vaccines used did not cause the adverse reactions such as hypersusceptibility and changes of feed intakes, and that 2 times of vaccinations of the vaccines all effectively enhanced the antibody levels, respectively, in which the No.Ⅲ vaccine stimulated antibody as rapid as the first vaccination was done while the No. I and No.Ⅱvaccines did not result in the antibody by the first vaccination. It was concluded that the No.

结果发现，三种供试的高致病性蓝耳病灭活疫苗均未引起供试猪发生过敏反应和采食量变化等不良反应；三种供试灭活疫苗经2次免疫后，均能提高抗体水平，其中供试疫苗Ⅲ在首次免疫后即能有效产生抗体，而供试疫苗I和供试疫苗Ⅱ在首次免疫后不能有效产生抗体。

Results In the major salivary glands of the fetus from 14-week to 32-week, the epithelial cells of striated and interlobular ducts showed NT-3 immunoreactivity. The immunoreactive intensity in the three major salivary glands was similar and it had no obvious chang from 14-week to 32-week.

结果 14~32周胎儿大唾液腺内纹状管和小叶间导管上皮细胞呈NT-3免疫阳性反应。3种大唾液腺中NT-3的免疫染色强度相似，且在胚胎发育的14~32周，免疫反应强度未见明显变化。

Abstract］ objective to compare the advantages and disadvantages of different samples and different methods in detection for banded krait venom.methods double immunodiffusion and enzymelinked immunosorbent assay were used as the methods to detect different samples of people and animal who were bit by banded krait.results in double immunodiffusion the samples were all negative;with elisa the samples of wound tissue liquid and blood were all positive.conclusion wound tissue liquid and blood are both fitting samples in detection for banded krait venom;double immunodiffusion isn't adapt to detect banded krait biting patient,but elisa is an good detection method.

目的 探讨银环蛇毒中毒检测中不同材料与不同方法的优缺点。方法采用双向免疫扩散法与间接elisa法对银环蛇毒中毒的人与动物的不同标本进行检测。结果双向免疫扩散法死者伤口皮肤组织液、死者心脏血清、死小猪伤口皮肤组织液及死小猪血清标本均未见免疫沉淀带；elisa法测标本均为阳性。结论银环蛇毒中毒检测中伤口皮肤组织液和血液都是合适的材料；双向免疫扩散法的检出率较低，而elisa法则是一种较好的检测方法。

RESULTS A eukaryotic expression system for high expression humanmutantCD59 were successfully set up : The recombinant PALTER-MAX plasmid containing human mutantCD59 cDNA and PCDNA plasmid were co-transfected into CHO cell by cation lipoid mediating method ;and the cells were grown in F12 medium containing 400ug/ml G418 for 14 days, positive clones were grown in RPMI1640 medium to get stable expressing cell lines . Highly expressing clones were selected by flow cytometry ,and were named PALTER-CD59-CHO1PALTER-CD59-CHO2 . Flow cytometry indicated that expression rates of PALTER-CD59-CHO1 and PALTER-CD59-CHO2 were 53.7%and 54.5%. Further more, Stable highly expressing CHO cell lines were more detected by immunocytochemistry and immunofluorescence technology . PALTER-CD59 -CHO1 and PALTER-CD59-CHO2 were grown in RPMI1640 to get a large of cells . CD59 protein were obtained by spalling PALTER- CD59- CHO1 and PALTER - CD59 - CHO2 cells . Stable highly expressing cells were further validated by SDS-PAGE, immunoblot analysis and solid enzyme immunoassay . PALTER - CD59 - CHO1 and PALTER - CD59 - CHO2 were glycated in RPMI1640 of 50mM ribose for 72 hours .BCECF releasing test indicted that the releasing rate of PALTER-CD59-CHO1 or PALTER-CD59-CHO2 was less high than PALTER-CHO ,and the releasing rate of glycated PALTER-CD59 -CHOI or PALTER-CD59-CHO2 was higher than unglycated ones . PALTER -CD59-CHO1 and PALTER -CD59 -CHO2 were glycated in RPMI1640 of 50mM ribose for 72 hours .BCECF releasing test indicted that the releasing rate of PALTER - CD59 - CHOI or PALTER - CD59 - CHO2 was less high than PALTER-CHO ,and the releasing rate of glycated PALTER-CD59-CHO1 or PALTER - CD5 9-CHO2 was higher than unglycated ones .

结果 成功构建突变人CD59的真核细胞表达系统：运用阳离子脂质体介导法将含有突变人CD59的PALTER—MAX重组质粒与PCDNA共转染入CHO细胞：用含有400ug／mlG418的F12培养基培养14天，筛选出稳定阳性表达克隆，RPMI1640培养基扩增获得稳定表达细胞株，并用流式细胞术进一步筛选出高效表达细胞株分别命名为PALTER—CD59—CH01、PALTER—CD59—CH02，表达率分别为53.7％、54.5％；应用免疫组化方法、免疫荧光技术进一步鉴定阳性细胞株；RPMI1640培养基大量扩增PALTER—CD59—CH01、PALTER—CD59—CH02细胞株，裂解细胞得到CD59蛋白质；通过SDS—PAGE凝胶电泳技术、免疫印迹技术、固相酶联免疫吸附试验验证了这两中文摘要个阳性细胞株CO59蛋白的高效表达；50mM核糖培养72小时，获得突变人CD59糖化细胞株，BCECF染料释放试验结果显示，PALTER一CD59一CHOI、pALTER一CD59一CHOZ细胞较PALTER一CHO细胞染料释放率低，未糖化PALTER一CD59一CHOI、PALTER一CD59一CHOZ细胞比较糖化后细胞染料释放率低。

Challenge was made after one month of immunization by vein. Re sults:The parasitemia of recombinant virus immunized monkey was 0.0 1%in first tw o days of post-challenge. No parasites were determined from third to 12th day. W hereas the parasitemia of control virus immunized-monkey and blank control monk ey rose progressively,went to 2.5%～6.0% at 6th～8th days of post-challenge, an d the t ime of parasitemia was 12～13 days.

结果： 在免疫后1个月攻虫，重组痘苗病毒免疫猴从第3天一直到第12 d的采血检查中均未发现疟原虫；非重组痘苗病毒免疫猴第3天后原虫感染率上升，第6天原虫感染率最高达到6.0%，而后原虫感染率逐渐下降，原虫持续时间为13天；空白对照猴第3天后原虫感染率也上升，第8天原虫感染率最高达到2.5%，而后原虫感染率逐渐下降，原虫持续出现时间为12 d。

In situ hybridization was used to observe the expression of the MCP-1 mRNA in the walls of the normal arteries and the aneurysms. Results: by the HE straining the walls of the ruptured aneurysms (10 cases) and unruptured ones (2 cases) were consisted of incrassated intima and connectivum extima.

免疫组化：MCP-1组：正常颅内动脉未见MCP-1阳性细胞，未破裂动脉瘤和破裂动脉瘤的阴性对照未见染色细胞。2例未破裂和10例破裂动脉瘤：MCP-1呈高表达，阳性细胞在动脉瘤壁内呈局灶聚集，间断分布动脉瘤内膜。

PART Ⅱ IMMUNOPATHOLOGICAL EVIDANCE OF SIALIC ACID STRUCTURE IN CAMPYLOBACTER JEJUNI AS THE CRITICAL ANTIGEN TO INDUCE PERIPHERAL NEUROPATHY To demonstrate the critical role of NANA structure in the pathogenesis of allergic peripheral neuropathy induced by Campylobacter jejuni and provide immunopathological evidence to confirm the supposition of molecular mimicry and cross-immunity between CJ LPS and gangliosides in nerve.

LPS免疫后第2周实验豚鼠的免疫血清中，抗LPS IgG抗体滴度均明显增高，第3周达高峰，第5周仍维持在峰水平，野生株和突变株LPS免疫血清中的抗-野生株LPS IgG抗体滴度较各自免疫前分别增高8倍和4倍，抗-突变株LPS IgG抗体滴度则较各自免疫前分别增高6.5倍和15倍；(2)全身免疫后第3周和第5周，野生株LPS免疫血清中检测到较免疫前增高6倍的抗-GM1 IgG抗体，而NANA缺失的突变株LPS免疫血清中一直未检测到抗-GM1 IgG抗体；(3)野生株LPS免疫组中有17.3％的坐骨神经原纤维发生以轴索变性为主（占65％）的免疫性损伤，与突变株LPS免疫组和对照组比较均有显著性差异。

Results The morphology of endocrine cells in digestive tract was of multiplicity.The density of 5-HT cells was the highest in the colon,but not found in the esophagus,cardia gastric and cecum.The results showed that SS cells were distributed in the pylorus mostly,but not detected in the cardia,colon,cecum and rectum.Gas positive cells were the most in the duodenums,while in the esophagus and cardia was not discovered.In the cardia VIP cells were maximum,but in the esophagus,duodenums and ileum did not appear.

结果 消化道中4种免疫阳性细胞形态多样，大多呈椭圆形和锥体形。5-HT阳性细胞数量以结肠最多，空肠和回肠次之，幽门腺区、十二指肠和直肠较少，食管、贲门腺区、胃底腺区和盲肠中未见；SS阳性细胞在幽门腺区数量最多，贲门腺区、结肠、盲肠和直肠中未见；Gas阳性细胞大量出现于十二指肠，在食管、贲门腺区和盲肠未见；除个别器官未见VIP阳性细胞外，在消化道的其余各段均有分布。

No immunostaining was seen in RPE. Double staining that Kir2. 1 and glutamine synthetase, Kir2. 1 and glutamine synthetase colocalized well. Intense Kir7. 1 immunolabeling was present on the apical surface of all RPE cells and appeared to extend over the length of the apical processes. Na〓, K〓-ATPase expression varied among RPE cells, but in highly expressing cells, it co-localized with Kir7. 1. Immunoreactivity of Kir2. 1、Kir4. 1 and Kir7. 1 acomplished by ABC immunohistochemistry in monkey and human retinae got the nearly same results as bovine.

间接免疫荧光组织化学显示，Kir2.1蛋白主要分布在Müller细胞与神经元相接触的细胞膜区域；与Müller细胞的特异性标记蛋白质抗谷氨酸合成酶抗体双重标记显示其分布特性重叠，在RPE未检测Kir2.1蛋白的免疫活性存在；Kir4.1蛋白集中分布于Müller细胞的内侧突起，与GS蛋白双重标记显示其分布特性重叠，RPE未检测Kir4.1蛋白的免疫活性存在；Kir7.1主要分布于RPE游离面及其突起的全长，与特异性标记RPE突起的Ezrin蛋白完全重叠，Na〓-K〓ATP酶在不同部位的RPE表达不同，Na〓-K〓ATP高表达的RPE细胞与Kir7.1的分布特性重叠。

The lumbar spinal cord in normal rat was immunohistochemically stained with ABC method using HAP1B antibody. Under light microscope, it was observed that HAP1 immunoreactants is mainly distributed in the pericaryon and neuropil in superficial lamella of the gray nucleus with little or no expression in other layers of the spinal horn. The substantia alba show no HAP1B immunoreactants.

对正常大鼠腰段脊髓进行HAP1B的ABC法免疫组织化学染色，光镜下观察显示，HAP1免疫反应产物主要分布在脊髓灰质背角浅层神经元胞体和神经毡内，灰质其他各层无或极少HAP1B表达，白质内未见明显HAP1B免疫反应产物。

However, as the name（read－only memory）implies, CD disks cannot be written onorchanged in any way.

然而，正如其名字所指出的那样，CD盘不能写，也不能用任何方式改变其内容。

Galvanizes steel pallet is mainly export which suits standard packing of European Union, the North America. galvanizes steel pallet is suitable to heavy rack. Pallet surface can design plate type, corrugated and the gap form, satisfies the different requirements.

镀锌钢托盘多用于出口，替代木托盘，免薰蒸，符合欧盟、北美各国对出口货物包装材料的法令要求；喷涂钢托盘适用于重载上货架之用，托盘表面根据需要制作成平板状、波纹状及间隔形式，满足不同的使用要求。