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131.
明胶-聚乳酸载药纳米微球的制备及其体外释药研究 总被引:21,自引:0,他引:21
采用复合乳液—溶剂挥发法制得明胶—聚乳酸载五氟脲嘧啶(5—Fu)微球,以混合型乳化剂Tween—80:Span—80=5:1—作为初乳乳化剂,O—羧甲基壳聚糖作为复乳乳化剂,考察了明胶—聚乳酸载药微球的制备条件对微球的成球性、药物包封率及体外释药的影响。结果表明乳化剂的选择、内部水相药物浓度和PLA分子量等均对载药微球的结构与性能产生影响,经优化条件得到了成球性和体外释放都比较好的载药微球。 相似文献
132.
Farilla L Tiberti C Luzzago A Yu L Eisenbarth GS Cortese R Dotta F Di Mario U 《European journal of immunology》2002,32(5):1420-1427
Autoantigenic epitope mapping represents a critical issue in autoimmune diseases. The islet tyrosine phosphatase-like protein IA-2/ICA512bdc is a major autoantigen in type 1 diabetes (IDDM), but the epitopes responsible for autoantibody binding have been only partially defined. The aim of our study was to identify ICA512bdc epitopes, and in particular mini-epitopes, utilizing a novel strategy for autoimmune diseases. The study was performed in three sequential steps: (1) construction of a lambda-phage surface-displayed ICA512bdc cDNA library with the methodology of tagged random priming with peptides displayed as a fusion to the C terminus of the capsid protein D; (2) affinity selection of the resulting library, followed by immunoscreening, enzyme-linked immunosorbent assay and sequence analysis of positive clones, and (3) radioimmunoprecipitation to detect autoantibodies to the selected clones. This strategy resulted in the identification of two epitopes (IA-2 residues 761 - 964 and 929 - 979), which were recognized by 100 % and 62.9 % ICA512bdc-positive IDDM patients, respectively. Interestingly, the larger clone was detected also by a proportion (16.7 %) of new onset ICA512bdc-negative patients, thus suggesting that this region contains not only the main autoantigenic repertoire of ICA512bdc molecule, but is able to detect IA-2 autoantibodies in even higher percentages of patients. In addition, this study showed the existence of multiple epitopes located in the C-terminal domain of the IA-2 protein, one of which is formed by the 50 C-terminal amino acids, and provided evidence that the strategy used represents a valid tool for identification of epitopes within autoantigenic molecules. 相似文献
133.
Jacqueline Girard Nam Hai Chua Pierre Bennoun Gregory Schmidt Monique Delosme 《Current genetics》1980,2(3):215-221
Summary Genetic analysis of 25 nuclear mutants defective in the chlorophyll-protein complex CP1 was undertaken. The mutants belong to 13 complementation groups scattered throughout the nuclear genome. All these mutants lack the apoprotein of CP1 and, in addition, a specific set of six low molecular weight thylakoid polypeptides. System I particles obtained by treating WT thylakoid membranes with detergent specifically contain those polypeptides which the mutants lack. These observations suggest that a particular sub-structure of the thylakoid membrane associated with the photosystem I activity is missing from all 25 mutants studied, and that this general phenotype can result from mutation at any one of several unlinked Mendelian loci. 相似文献
134.
用活化的人B细胞株3D5细胞免疫BALB/C小鼠,取小鼠脾脏细胞与SP2/0细胞融合,融合后细胞置甲基纤维素半固体培养基生长。以0.5%甲醛处理的3D5细胞和CEM细胞包被酶细胞反应阳性而与CEM细胞反应阴性的克隆。再经间接免疫荧光染色后,用流式细胞仪复测以上所得33个阳性克隆,结果3D5阳性CEM阴性者27例,占81.82%,表明CELISA法是一个粗筛抗人B细胞分化抗原的简便有效方法。 相似文献
135.
Yang JQ Chun T Liu H Hong S Bui H Van Kaer L Wang CR Singh RR 《European journal of immunology》2004,34(6):1723-1732
Mechanisms responsible for the development of autoimmune skin disease in humans and animal models with lupus remain poorly understood. In this study, we have investigated the role of CD1d, an antigen-presenting molecule known to activate natural killer T cells, in the development of inflammatory dermatitis in lupus-susceptible MRL-lpr/lpr mice. In particular, we have established MRL-lpr/lpr mice carrying a germ-line deletion of the CD1d genes. We demonstrate that CD1d-deficient MRL-lpr/lpr mice, as compared with wild-type littermates, have more frequent and more severe skin disease, with increased local infiltration with mast cells, lymphocytes and dendritic cells, including Langerhans cells. CD1d-deficient MRL-lpr/lpr mice had increased prevalence of CD4(+) T cells in the spleen and liver and of TCR alpha beta (+)B220(+) cells in lymph nodes. Furthermore, CD1d deficiency was associated with decreased T cell production of type 2 cytokines and increased or unchanged type 1 cytokines. These findings indicate a regulatory role of CD1d in inflammatory dermatitis. Understanding the mechanisms by which CD1d deficiency results in splenic T cell expansion and cytokine alterations, with increased dermal infiltration of dendritic cells and lymphocytes in MRL-lpr/lpr mice, will have implications for the pathogenesis of inflammatory skin diseases. 相似文献
136.
利用木瓜蛋白酶分别制备了抗汉坦病毒鼠源性单克隆抗体(mAb)3G1和3D8F(ab′)2片段。通过WaterDEAE40HR阴离子交换色谱柱纯化后,非还原型SDSPAGE呈现单一条带,相对分子质量(Mr)约100000。两种F(ab′)2片段均具有良好的血凝抑制活性、病毒中和活性及对汉坦病毒感染乳鼠的保护作用 相似文献
137.
Zuochen Du Anwei Chen Lu Huang Xin Dai Qiuyue Chen Di Yang Liling Li Heather Miller Lisa Westerberg Yuan Ding Xuemei Tang Masato Kubo Liping Jiang Xiaodong Zhao Hua Wang Chaohong Liu 《The Journal of allergy and clinical immunology》2021,147(5):1907-1923.e6
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138.
Xin-Tong Wei Gui-Juan Feng Hong Zhang Qian Xu Jing-Jing Ni Min Zhao Xiao-Lin Yang Qing Tian Hui Shen Rong Hai Hong-Wen Deng Lei Zhang Yu-Fang Pei 《European journal of human genetics : EJHG》2021,29(4):553
Osteoporosis and obesity are two severe complex diseases threatening public health worldwide. Both diseases are under strong genetic determinants as well as genetically correlated. Aiming to identify pleiotropic genes underlying obesity and osteoporosis, we performed a bivariate genome-wide association (GWA) meta-analysis of hip bone mineral density (BMD) and total body fat mass (TBFM) in 12,981 participants from seven samples, and followed by in silico replication in the UK biobank (UKB) cohort sample (N = 217,822). Combining the results from discovery meta-analysis and replication sample, we identified one novel locus, 17q21.31 (lead SNP rs12150327, :g.44956910G > A, discovery bivariate P = 4.83 × 10−9, replication P = 5.75 × 10−5) at the genome-wide significance level (ɑ = 5.0 × 10−8), which may have pleiotropic effects to both hip BMD and TBFM. Functional annotations highlighted several candidate genes, including KIF18B, C1QL1, and PRPF19 that may exert pleiotropic effects to the development of both body mass and bone mass. Our findings can improve our understanding of the etiology of osteoporosis and obesity, as well as shed light on potential new therapies.Subject terms: NC_000017.11Genome-wide association studies, Gene expression profiling 相似文献
139.
目的:采用磁微粒分离酶联免疫荧光(MEIF)分析技术建立一种简便、高敏感性、定量检测人血清胰岛素(insulin)的新方法.方法:选用2株识别人胰岛素不同表位的单克隆抗体(mAb).一株mAb用异硫氰酸荧光素(FITC)标记, 另一株用碱性磷酸酶(AP)标记;偶联羊抗FITC抗体的磁珠用作固相分离载体, 4-甲基磷酸伞型酮用作荧光底物.结果:成功建立了定量检测人血清胰岛素的MEIF, 灵敏度2.0 μIu/mL, 线形范围0~188.52 μIu/mL, 批内变异系数(CV)为4.3%~5.2%, 批间CV为2.6%~9.5%, 稀释回收率为93%~117%, 加标回收率为94%~113%.实际样品的测定结果与倍爱康公司商品化人insulin磁分离发光系统检测试剂盒的检测结果比较, 具有良好的相关性.结论:MEIF定量测定人insulin方法成本低、灵敏度高、稳定性好, 在临床免疫检测领域具有广阔的应用前景. 相似文献
140.
我国脑膜炎奈瑟菌孔蛋白PorA、PorB的多态性分析 总被引:1,自引:0,他引:1
胡源 邵祝军 闫笑梅 李波清 赵飞 肖迪 任军 郑明寰 樊春祥 何利华 徐丽 顾一心 姜海 郭凤华 李马超 陆美娟 陈霞 邹清华 孟凡亮 张建中 《中华微生物学和免疫学杂志》2007,27(3):218-221
目的以蛋白质组学研究为基础,分析2003—2005年我国流脑暴发流行期间C群脑膜炎奈瑟菌菌株特征,建立以致病性相关蛋白多态性为目标的新分型方法。方法利用双向电泳和MALDI-TOF质谱鉴定分析2003—2005年流脑流行期内分离的66株C群脑膜炎奈瑟菌菌株及2株参考菌株的蛋白表达,重点分析与致病性相关的蛋白多态性特征。结果根据孔蛋白PorA、PorB在双向电泳中的多态性,建立了12个特征菌型。安徽菌株的PorA和PorB蛋白电泳谱型显示出了高度的一致性,而其他地区的菌株则显示出高度的多态性。结论PorA和PorB蛋白2-DE电泳谱型可以作为一种新的菌株分型方法,可能在菌型变迁检测和流脑暴发预警中具有重要应用前景。 相似文献