白细胞

To elucidate the molecular basis of the attenuation ofDLA-EIAV in virulence thus provide theory foundation for designing HIV vaccine, thewhole genomes of DLA-EIAV and EJAV L provirus were cloned and sequenced. Aninfectious molecular clone derived from DLA-ELAV was constructed and characterized.Three DLA-EIAV/ L chimeric viruses were constructed. Promoting efficacy of the longterminal repeat of the DLA-EIAV was charactenzed.

为了揭示我国马传贫弱毒疫苗毒力致弱及免疫保护的分子机制，为人免疫缺陷病毒及其它慢病毒的免疫预防提供借鉴，我们对马传贫驴白细胞弱毒及其亲本马强毒EIAV L株前病毒进行了全基因克隆和序列测定，比较分析了二者的前病毒基因组核苷酸序列，在此基础上构建了EIAV驴白细胞弱毒株的感染性分子克隆和三株含有EIAV强/弱毒嵌合病毒基因组的重组质粒，并对EIAV弱毒株长末端重复序列的启动子活性进行了初步研究。

To elucidate the molecular basis of the attenuation ofDLA-EIAV in virulence thus provide theory foundation for designing HIV vaccine,thewhole genomes of DLA-EIAV and EIAV L provirus were cloned and sequenced.Aninfectious molecular clone derived from DLA-EIAV was constructed and characterized.Three DLA-EIAV/L chimeric viruses were constructed.Promoting efficacy of the longterminal repeatof the DLA-EIAV was characterized.

为了揭示我国马传贫弱毒疫苗毒力致弱及免疫保护的分子机制，为人免疫缺陷病毒及其它慢病毒的免疫预防提供借鉴，我们对马传贫驴白细胞弱毒及其亲本马强毒EIAV L株前病毒进行了全基因克隆和序列测定，比较分析了二者的前病毒基因组核苷酸序列，在此基础上构建了EIAV驴白细胞弱毒株的感染性分子克隆和三株含有EIAV强/弱毒嵌合病毒基因组的重组质粒，并对EIAV弱毒株长末端重复序列的启动子活性进行了初步研究。

Gene coding for matrix protein (p15) of donkey leukocyte attenuated vaccine strain of equine infectious anemia virus was cloned from its proviral DNA obtained from the vaccine strain infected donkey leukocyte cultures,and expressed in E.coli.

从感染驴白细胞的马传贫驴白细胞弱毒疫苗株前病毒DNA中克隆了编码基质蛋白(p1 5 )的基因，并在大肠杆菌中进行了表达。

Methods Blood samples of fifty-two patients who underwe n t open heart surgery with CPB were collected from right internal jugular vein at p oints as pre-CPB, rewarming, aortic declamping, 6 hours and 24 hours after CPB. Cytokines, iNOS, S-100 and NSE were assayed accurately. In addition, its corre lation between them were also analysed.

方法于 CPB前、复温即刻、主动脉开放和 CPB后 6、2 4小时采集 5 2例心脏病患者颈内静脉血，检测 S- 10 0蛋白和 NSE的浓度，并将其与炎性细胞因子白细胞介素- 6 (IL- 6 )、白细胞介素- 8(IL- 8)、肿瘤坏死因子-α和诱导型一氧化氮合成酶的浓度变化进行相关性分析。

The results showed that the starved fish had significant higher white-cell counts than the fed fish,the peak value occurring 20 d after starvation.There were higher multiplication and efficiency of transformation in the lymphocytes in the starved fish than those in the fed fis...

结果表明：饥饿后红鳍东方鲀外周血中白细胞的数量明显高于正常投喂组，且在饥饿20 d时白细胞的数量达到最大值；饥饿后脾脏中淋巴细胞的增殖转化能力与转化率比正常投喂组高，饥饿10 d时达到最大值，随着饥饿时间的延长，淋巴细胞的转化率逐渐降低；饥饿后脾脏中巨噬细胞的吞噬活性与吞噬率均高于正常投喂组，且在饥饿20 d时达到最大值。

Methods The present study has been carried out using NaCMC injected into the mice's abdominal cavity to cause inflammation and induce white blood cell migration,varnishing DNFB to induce mice's DTH,injecting colloid activated carbon suspension into mice's tail vein,with 10% of sheep RBC injected into the abdomen to immunize mice.We observed inhibitory function of Liyankang granule on NaCMC to cause inflammation and induce white blood cell migration,the effect of DNFB on inducing mice's DTH and the effect on clearance speed of carbon particle in mice's blood and serum agglution of mice.

采用大鼠腹腔注射羟甲基纤维素钠致炎诱发白细胞游走，涂抹二硝基氟苯诱导小鼠迟发型超敏反应，小鼠尾静脉注射胶体碳悬液，腹腔注射10%羊红细胞免疫小鼠，观察小儿利咽康颗粒剂对羟甲基纤维素钠致炎诱发白细胞游走的抑制作用，对二硝基氟苯诱导小鼠迟发型超敏反应、对小鼠血中碳粒清除速度、对小鼠血清凝集素的影响。

Methods The present study has been carried out using NaCMC injected into the mice's abdominal cavity to cause inflammation and induce white blood cell migration,varnishing DNFB to induce mice's DTH,injecting colloid activated carbon suspension into mice's tail vein,with 10% of sheep RBC injected into the abdomen to immunize mice.

采用大鼠腹腔注射羟甲基纤维素钠致炎诱发白细胞游走，涂抹二硝基氟苯诱导小鼠迟发型超敏反应，小鼠尾静脉注射胶体碳悬液，腹腔注射10%羊红细胞免疫小鼠，观察小儿利咽康颗粒剂对羟甲基纤维素钠致炎诱发白细胞游走的抑制作用，对二硝基氟苯诱导小鼠迟发型超敏反应、对小鼠血中碳粒清除速度、对小鼠血清凝集素的影响。

Department of Basic Medical Sciences,College of Vocational Technology,Liaoning University of TCM,Shenyang 110101.China Objective To observe immune regulation effect of Liyankang granule on children.Methods The present study has been carried out using NaCMC injected into the mice's abdominal cavity to cause inflammation and induce white blood cell migration,varnishing DNFB to induce mice's DTH,injecting colloid activated carbon suspension into mice's tail vein,with 10% of sheep RBC injected into the abdomen to immunize mice.We observed inhibitory function of Liyankang granule on NaCMC to cause inflammation and induce white blood cell migration,the effect of DNFB on inducing mice's DTH and the effect on clearance speed of carbon particle in mice's blood and serum agglution of mice.

采用大鼠腹腔注射羟甲基纤维素钠致炎诱发白细胞游走，涂抹二硝基氟苯诱导小鼠迟发型超敏反应，小鼠尾静脉注射胶体碳悬液，腹腔注射10%羊红细胞免疫小鼠，观察小儿利咽康颗粒剂对羟甲基纤维素钠致炎诱发白细胞游走的抑制作用，对二硝基氟苯诱导小鼠迟发型超敏反应、对小鼠血中碳粒清除速度、对小鼠血清凝集素的影响。

In the course of experimental study on re-perfusion of ischemic skeletal-muscle graft, Zamboni found that HBO could reduce leukocyte adhering to endothelia and infiltrating.

有学者在对肌瓣移植的缺血再灌注损伤进行实验研究时发现：HBO能够减少白细胞与血管内皮细胞粘附，并减少白细胞的浸润，减轻局部的炎症反应，从而减轻肌瓣的缺血再灌注损伤。

Methods Explore the optimal concentration of phurbol-12-myristate-acetate and calcium ionophore (A23817) inducing time, and optimal concentration of biotinyl sheep anti mouce IgG (bio-SAM-IgG) and horse radish peroxidasestreptavidin. The CD4(superscript +) cell enriched from peripheral blood mononuclear cells using solid phase anti-CDs monoclonal antibodies were induced by PMA and A23817 under influence of monensin and harvested in vary hours.

从健康人外周血单个核细胞中富集CD4细胞，加入莫能霉素，用不同浓度的佛波醇酯和钙离子载体(A23817)诱导CD4细胞不同时间，比较其胞内表达白细胞介素－2(IL-2)/白细胞介素－4(IL-4)的细胞百分率，确定最适诱生条件；用不同稀释度的IL-2McAb、IL-4McAb、不同浓度的生物素化羊抗鼠IgG(bio-SAM IgG)和辣根过氧化物酶标记的链霉亲和素作棋盘配比试验，确认McAb、bio-SAM IgG和HRP-SA的最适浓度，根据上述结果建立了检测细胞内细胞因子的BSA-ICC法。

This one mode pays close attention to network credence foundation of the businessman very much.

这一模式非常关注商人的网络信用基础。

Cell morphology of bacterial ghost of Pasteurella multocida was observed by scanning electron microscopy and inactivation ratio was estimated by CFU analysi.

扫描电镜观察多杀性巴氏杆菌细菌幽灵和菌落形成单位评价遗传灭活率。