18 resultados para Flu vaccines

em Chinese Academy of Sciences Institutional Repositories Grid Portal


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合成了 6种单碳桥联的含芴 (Flu)茂 (Cp)基 B族茂金属催化剂 ,研究了它们催化烯烃聚合的能力 .通过 IR,1H NMR,EI-MS和元素分析对化合物进行了表征 .用所合成的茂金属化合物与 MAO所组成的催化体系对乙烯、丙烯的聚合进行了研究 .其中金属为 Ti的催化剂没有聚合活性或活性极低 .金属为 Zr的催化剂有一定的催化活性 ,用不同的催化剂得到的聚合物性质有一定的差异

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Edwardsiella tarda is an opportunistic pathogen that can infect humans, animal, and fish. Two E. tarda antigens, Eta6 and FliC, which are homologues to an ecotin precursor and the FliC flagellin, respectively, were identified by in vivo-induced antigen technology from a pathogenic E. tarda strain isolated from diseased fish. When used as a subunit vaccine, purified recombinant Eta6 was moderately protective against lethal challenge of E. tarda in a Japanese flounder model, whereas purified recombinant FliC showed no apparent immunciprotectivity. Similarly, DNA vaccines based on eta6 and fliC in the form of plasmids pEta6 and pFliC induced, respectively, moderate and marginal protection against E. tarda infection. To improve the vaccine efficacy of eta6, a chimeric DNA vaccine, pCE6, was constructed, which encodes Eta6 fused in-frame to FliC. pCE6 was found to induce significantly higher level of protection than pEta6. Likewise, another chimeric DNA vaccine, pCE18, which expresses FliC fused to a previously identified E. tarda antigen Et18, elicited significantly stronger protective immunity than the DNA vaccine based on et18 alone. Fish immunized with pEta6 and pCE6 produced specific serum antibodies and exhibited significantly enhanced expression of the genes encoding elements that are involved in both innate and adaptive immune responses. Furthermore, the induction magnitudes of most of these genes were significantly higher in pCE6-vaccinated fish than in pEta6-vaccinated fish. (C) 2009 Elsevier Ltd. All rights reserved.

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The hierarchial structure and mathematical property of the simplified Navier-Stokesequations (SNSE) are studied for viscous flow over a sphere and a jet of compressible flu-id. All kinds of the hierarchial SNSE can be divided into three types according to theirmathematical property and also into five groups according to their physical content. Amultilayers structure model for viscous shear flow with a main stream direction is pre-sented. For the example of viscous incompressible flow over a flat plate there existthree layers for both the separated flow and the attached flow; the character of thetransition from the three layers of attached flow to those of separated flow is elucidated.A concept of transition layer being situated between the viscous layer and inviscidlayer is introduced. The transition layer features the interaction between viscous flow andinviscid flow. The inner-outer-layers-matched SNSE proposed by the present author inthe past is developed into the layers matched (LsM)-SNSE.

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合成了具有大π共轭性的对称型芴类衍生物9,9-二(2-乙基已基)-2,7-(2-(4-甲氧基)苯-2,1-乙烯基)芴(简写为MO-F1u—MO)。通过元素分析、质谱、紫外-可见光谱和红外光谱对其进行了表征。测试了该染料在乙腈、二氯甲烷、四氢呋喃和正己烷4种不同极性溶剂中的线性吸收光谱和单光子荧光谱。结果发现溶剂效应对吸收光谱和荧光光谱表现出不同程度的影响,对产生这些光谱行为的主要原因进行了讨论。

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For developing efficient vaccines, it is essential to identify which amino acid changes are most important to the survival of the virus. We investigate the amino acid substitution features in the Avian Infectious Bronchitis Virus (AIBV) antigenic domain o

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Non-human primates such as Chinese rhesus macaques are the favorable models for preclinical study of potential therapeutic drugs, vaccines and mechanisms of human diseases. Little is known about the normal levels of leukocyte subpopulations of Chinese rhe

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有关水生植物净化污水的研究已有广泛报道,但现有成果多来源于静态的室内研究,所用植物多为生活型接近的物种。为了比较不同生活型植物对河道污水的原位净化效果差异,构建了由水芹菜(Oenanthe javanica)、马尾草(Equisetum flu-viatile)、伊乐藻(Elodea Canadensis Michx.)和狐尾藻(Myriophyllum verticillatum L.)等4种不同生活型水生植物组成的水生植物塘系统,研究塘中不同植物对滇池入湖河道污水中氮、磷等指标去除效能的差异。结果表明

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本论文分为两部分,第一部分合成一些新型茂稀土催化剂。一共合成出四类22种稀土金属有机配合物。第二部分尝试了茂基稀土配合物对甲基丙烯酸甲酯(MMA)、丙烯腈(AN)、4-乙烯基吡啶(4-VP)、已内酯(CL)的聚合,研究了其聚合规律,并对其聚合物进行了表征。主要结果如下:1. 合成出四类22种稀土金属有机配合物:第一类:氯化稀土配合物(C_9H_7)_2LnCl(THF)_n (Ln = Y,Yb,Nd,Sm),Me_2Si(Ind)_2 YCl(THF)_n,Me_2Si(Flu)_2YCl(THF)_n, Me_2Si(Ind)(Flu)YCl(THF)_n。第二类:稀土胺化物(C_9H_7)_2LnN(i-Pr)_2(THF) (Ln = Y,Yb), Me_2Si(Ind)_2YN(i-Pr)_2,Me_2Si(Flu)_2Y N(i-Pr)_2, Me_2Si(Ind)(Flu)YN(i-Pr)_2。第三类:稀土与铝双金属配合物(C_9H_7)_2Y(μ-Et)_2AlEt_2,Me_2Si(Flu)_2Y(μ-Et)_2AlEt_2, Me_2Si(Ind)(Flu)Y(μ-Et)_2AlEt_2,(C_9H_7)_2Sm(μ-Me)_2AlMe_2, (C_9H_7)_2Sm(μ-Et)_2AlEt_2。第四类:二价钐配合物(C_9H_7)_2Sm(THF)_3,(C_(13)H_9)_2Sm(THF)_2, Me_2Si(Flu)_2Sm(THF)_x,Me_2Si(Ind)(Flu)Sm (THF)_x, (CH_2)_2(fLU)_2Sm(THF)_x。对每类配合物分别进行了核磁、红外及紫外分析。2.茂稀土配合物催化极性单体聚合(1)甲基丙烯酸甲酯(MMA)聚合 首次发现(C_9H_7)_2Y(μ-Et)_2AlEt_2, (C_9H_7)_2LnN(i-Pr)_2(THF) (Ln = Y,Yb), Me_2Si(Ind)_2YN(i-Pr)_2,Me_2Si(Flu)_2YN(i-Pr)_2, Me_2Si(Ind)(Flu)YN(i-Pr)_2 MMA聚合均表现出极高的催化活性,其中以(C_9H_7)_2Y(μ-Et)_2AlEt_2催化MMA所得的PMMA全同含量(mm)可达94.8%。(2)丙烯腈(AN)聚合:首次发现(C_9H_7)_2Y(μ-Et)_2AlEt_2,(C_9H_7)_2LnN(i-Pr)_2(THF) (Ln=Y,Yb)对AN聚合表现出较高的催化活性,并且发现往此催化体系中加入添加剂PhONa,基催化活性及分子量都明显提高。其聚合物的立构规整性用~(13)C-NMR谱进行了表征,发现聚合物的结构均为无规结构。(3)4-乙烯基吡啶(4-VP)聚合:首次发现(C_9H_7)_2Y(μ-Et)_2AlEt_2,(C_9H_7)_2Sm(THF)_3对4-VP聚合表现出很好的催化活性,并且发现单体浓度及催化剂用量对4-VP聚合有较大的影响。此外,一些桥联配体的二价钐配合物Me_2Si(Flu)_2Sm(THF)_x,Me_2Si(Ind)(Flu)Sm(THF)_x, (CH_2)_2(Flu)_2Sm(THF)_x也能催化4-VP聚合,但其催化活性较低。(4)已内酯(CL)聚合:比较了各类茂稀土催化剂对己内酯开环聚合的催化活性。发现Ind_2Y(μ-Et)_2AlEt_2,Ind_2YN(i-Pr)_2(THF), Me_2Si(Ind)(Flu)YN(i-Pr)_2(THF),Me_2Si(Flu)_2YN(i-Pr)_2(THF), Me_2Si(Ind)_2YN(i-Pr)_2(THF),Ind_2Sm(THF)_x, Me_2Si(Flu)_2Sm(THF)_x,Me_2Si(Ind)(Flu)Sm(THF)_x, (CH_2)_2(Flu)_2Sm(THF)_x均能有效地催化己内酯开环聚合,二价稀土金属配合物的催化活性要比三价稀土金属配合物高。

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therapeutic drugs, vaccines and mechanisms of human diseases. Little is known about the normal levels of leukocyte subpopulations of Chinese rhesus macaques. To obtain these data, 100 blood samples from Chinese rhesus macaques were collected. The normal range of major leukocyte subpopulations, such as T lymphocytes, B lymphocytes, monocytes, myeloid dendritic cells (mDCs) and plasmacytoid dendritic cells (pDCs), were quantitatively analyzed by flow cytometry through BD trucount tubes. The influence of age and sex on the cell counts of leukocyte subpopulations was analyzed. The counts of CD3+ T cells, CD3+CD4+ T cells, CD3+CD8+ T cells and B cells decreased with age, but those of monocytes, mDCs and pDCs had no significant correlation with age. Significant differences existed in the cell counts of most leukocyte subpopulations between the male and female groups except pDCs. Furthermore the values of the females were higher than those of the males. The study provided basic information about the leukocyte subpopulations of Chinese rhesus macaques, and it may be valuable for immunobiological study of Chinese rhesus macaques. Cellular & Molecular Immunology. 2009;6(6):433-440.

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Fluorenyl modified N-heterocyclic carbene ligated rare earth metal bis(alkyl) complexes, (Flu-NHC)Ln(CH2SiMe3)2 (Flu-NHC = (C13H8CH2CH2(NCHCCHN)C6H2Me3-2,4,6); Ln = Sc (1a); Ln = Y (1b); Ln = Ho (1c); Ln = Lit (1d)), were synthesized and fully characterized by NMR and X-ray diffraction analyses. Complexes Ib-d with the activation of (AlBu3)-Bu-i and [Ph3C][B(C6F5)4] exhibited high activity, medium syndio-but remarkably high 3,4-regio-selectivity, and the unprecedented livingness for the polymerization of isoprene. Such distinguished catalytic performances could be maintained under various monomer-to-initiator ratios (500-5000) and broad polymerization temperatures (25-80 degrees C).

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Rare earth metal bis(alkyl) complexes attached by fluorenyl modified N-heterocyclic carbene (NHC) (Flu-NHC)Ln(CH2SiMe3)(2) (Flu-NHC = (C13H8CH2CH2(NCHCCHN)C6H2Me3-2,4,6); Ln = Sc (2a); Y (2b); Ho (2c); Lu (2d)), ((tBu)Flu-NHC)Ln(CH2SiMe3)(2) ((tBu)Flu-NHC = 2,7-(Bu2C13H6CH2CH2)-Bu-t(NCHCCHN)C6H2Me3-2,4,6; Ln = Sc (1a); Lu (1d)) and attached by indenyl modified N-heterocyclic carbene (Ind-NHC)Ln(CH2SiMe3)(2) (Ind-NHC = C9H6CH2CH2(NCHCCHN)C6H2Me3-2,4,6; Ln = Sc (3a); Lu (3d)), under the activation of (AlBu3)-Bu-i and [Ph3C][B(C6F5)(4)], showed varied catalytic activities toward homo- and copolymerization of ethylene and norbornene. Among which the scandium complexes, in spite of ligand type, exhibited medium to high catalytic activity for ethylene polymerization (10(5) g mol(Sc)(-1) h(-1) atm(-1)), but all were almost inert to norbornene polymerization. Remarkably, higher activity was found for the copolymerization of ethylene and norbornene when using Sc based catalytic systems, which reached up to 5 x 10(6) g mol(Sc)(-1) h(-1) atm(-1) with 2a. The composition of the isolated copolymer was varying from random to alternating according to the feed ratio of the two monomers (r(E) = 4.1, r(NB) = 0.013).

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The polymerization of butadiene(Bd), isoprene(Ip) and styrene(St) has been examined using the six catalyst systems composed of lanthanocene, (C5H9Cp)(2)NdCl(I), (C5H9Cp)(2)SmCl(II), (MeCp)(2)SmOAr'(III), (Ind)(2)NdCl(IV), Me2Si(Ind)(2)NdCl(V) and (Flu)(2)NdCl(VI), and methylaluminoxane(MAO) respectively. All of them can be used to form the polyisoprene with molecular weights of 1 to 10 thousand and cis-1,4-unit contents of 41 to 47%. (I), (II) and (III) of them can be also used to form the polybutadiene with molecular weights of 10 to 20 thousand and cis-1,4-unit contents of 62 to 78%. In addition, the catalysts from (II) to (V) are still active for St polymerization and (II) of them gives a syndio -rich random polystyrene. It is noteworthy that (II) and (III) are active for homopolymerization of Bd, Ip and St in the same polymerization condition.

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Aims: Genes uniquely expressed in vivo may contribute to the overall pathogenicity of an organism and are likely to serve as potential targets for the development of new vaccine. This study aims to screen the genes expressed in vivo after Vibrio anguillarum infection by in vivo-induced antigen technology (IVIAT). Methods and Results: The convalescent-phase sera were obtained from turbot (Scophthalmus maximus) survived after infection by the virulent V. anguillarum M3. The pooled sera were thoroughly adsorbed with M3 cells and Escherichia coli BL21 (DE3) cells. A genomic expression library of M3 was constructed and screened for the identification of immunogenic proteins by colony immunoblot analysis with the adsorbed sera. After three rounds of screening, 19 putative in vivo-induced (ivi) genes were obtained. These ivi genes were catalogued into four functional groups: regulator/signalling, metabolism, biological process and hypothetical proteins. Three ivi genes were insertion-mutated, and the growth and 50% lethal dose (LD50) of these mutants were evaluated. Conclusions: The identification of ivi genes in V. anguillarum M3 sheds light on understanding the bacterial pathogenesis and provides novel targets for the development of new vaccines and diagnostic reagents. Significance and Impact of the Study: To the best of our knowledge, this is the first report describing in vivo-expressed genes of V. anguillarum using IVIAT. The screened ivi genes in this study could be new virulent factors and targets for the development of vaccine, which may have implications for the development of diagnostic regents.

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Aims: Genes uniquely expressed in vivo may contribute to the overall pathogenicity of an organism and are likely to serve as potential targets for the development of new vaccine. This study aims to screen the genes expressed in vivo after Vibrio anguillarum infection by in vivo-induced antigen technology (IVIAT). Methods and Results: The convalescent-phase sera were obtained from turbot (Scophthalmus maximus) survived after infection by the virulent V. anguillarum M3. The pooled sera were thoroughly adsorbed with M3 cells and Escherichia coli BL21 (DE3) cells. A genomic expression library of M3 was constructed and screened for the identification of immunogenic proteins by colony immunoblot analysis with the adsorbed sera. After three rounds of screening, 19 putative in vivo-induced (ivi) genes were obtained. These ivi genes were catalogued into four functional groups: regulator/signalling, metabolism, biological process and hypothetical proteins. Three ivi genes were insertion-mutated, and the growth and 50% lethal dose (LD50) of these mutants were evaluated. Conclusions: The identification of ivi genes in V. anguillarum M3 sheds light on understanding the bacterial pathogenesis and provides novel targets for the development of new vaccines and diagnostic reagents. Significance and Impact of the Study: To the best of our knowledge, this is the first report describing in vivo-expressed genes of V. anguillarum using IVIAT. The screened ivi genes in this study could be new virulent factors and targets for the development of vaccine, which may have implications for the development of diagnostic regents.

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Molecular biotechnology of marine algae is referred to as the biotechnology on the identification, modification, production and utilization of marine algal molecules. It involves not only the manipulation of macromolecules such as DNA, RNA and proteins, but also deals with low molecular weight compounds such as secondary metabolites. In the last decade, molecular systematic researches to investigate the relationship and to examine the evolutionary divergence among Chinese marine algae have been carried out by Chinese scientists. For example, RAPD has been widely used in several laboratories to elucidate genetic variations of the reds, such as Porphyra, Gracilaria, Grateloupia and the greens such as Ulva and Enteromorpha. Some important data have been obtained. The study on molecular genetic markers for strain improvement is now in progress. In 1990s, genetic engineering of economic seaweeds such as Laminaria, Undaria, Porphyra, Gracilaria and Grateloupia has been studied in China. For Laminaria japonica, the successfully cultivated kelp in China, a model transformation system has been set up based on the application of plant genetic techniques and knowledge of the algal life history. Progress has been made recently in incorporating a vaccine gene into kelp genome. Evidence has been provided showing the expression of gene products as detectable vaccines. In the present paper, the progress of molecular biotechnological studies of marine algae in China, especially researches on elucidating and manipulating nucleic acids of marine algae, are reviewed.