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单纯疱疹病毒DNA在多形红斑皮损中的表达
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作者 刘恩让 张建军 +1 位作者 王香玲 张磐谏 《岭南皮肤性病科杂志》 1997年第2期4-5,共2页
应用聚合酶链式反应方法,对26例多形红斑组织中的单纯疱疹病毒DNA进行检测。18例为阳性,阳性率为72%。对照组选择结节性红斑11例,固定性药疹8例,均为阴性。结果对研究单纯疱疹病毒在多形红斑发病中的意义和临床治疗有指导价值。
关键词 多形红斑 单纯疱疹病毒dna 聚合酶链式反应 病理学 PCR法
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Quantitation of Genital Herpes Virus DNA by Polymerase Chain Reaction and ELISA 被引量:8
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作者 程培华 《Chinese Journal of Sexually Transmitted Infections》 2002年第1期27-30,共4页
Objective: To detect and quantitate genital herpes simplexvirus (HSV) DNA in specimens from 100 patients clinicallydiagnosed with genital herpes. Methods: Polymerase Chain Reaction (PCR) andenzyme-linked immunosorbent... Objective: To detect and quantitate genital herpes simplexvirus (HSV) DNA in specimens from 100 patients clinicallydiagnosed with genital herpes. Methods: Polymerase Chain Reaction (PCR) andenzyme-linked immunosorbent assay (ELISA) were used witha standard curve of DNA copies of HSV as quantitativecontrast. Results: Ninety-three cases were confirmed HSV positiveand 7 cases were found to be negative. There were 58 cases ofHSV-2 (62.4%) and 35 cases of HSV-1(37.6%) among the 93positive cases. The number of DNA plasmids ranged from 115to 1.1×10~5 per 250μL among the 93 positive samples (mean=7.1×10~4/250μL). The number of HSV DNA plasmids rangedfrom 136 to 1.1×10~5 copies per 250μL(mean=7.6×10~4) amongthose with HSV-2, and 115 to 9.4×10~4 per 250μL(mean=6.3×10~4) among those with HSV-1. Meanwhile 10μL ofextracted and dissolved DNA randomly taken from 8 each ofHSV-2 and HSV-1 samples were tested. The number of HSV-2DNA plasmids ranged from 35 copies to 2.7×10~4 (Mean=1.8×10~4) and the number of HSV-1 DNA ranged from 29 to2.5×10~4 (Mean=1.6×10~4). In the 7 negative cases, the quantityof HSV plasmids was zero. Conclusion: The sensitivity of ELISA quantitation (93%) isequal to that of Southern blot. The sensitivity of PCR fordiagnosis is 91%, and 88% for PCR typing. 展开更多
关键词 HSV dna quantitation PCR ELISA Southern blot
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小鼠MIP-1α真核表达质粒的构建及在HSV-II核酸疫苗中的应用 被引量:4
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作者 邵文爱 李晓眠 《细胞与分子免疫学杂志》 CAS CSCD 北大核心 2006年第3期286-289,共4页
目的构建小鼠巨噬细胞炎性蛋白-1α(MIP-1α)的真核表达质粒,观察其作为分子佐剂对单纯疱疹病毒II型(HSV-II)DNA疫苗免疫效果的影响。方法以LPS刺激RAW264.7细胞提取总RNA。采用RT-PCR扩增出MIP-1α基因的全部编码序列,利用克隆载体pUCm... 目的构建小鼠巨噬细胞炎性蛋白-1α(MIP-1α)的真核表达质粒,观察其作为分子佐剂对单纯疱疹病毒II型(HSV-II)DNA疫苗免疫效果的影响。方法以LPS刺激RAW264.7细胞提取总RNA。采用RT-PCR扩增出MIP-1α基因的全部编码序列,利用克隆载体pUCm-T,将其亚克隆入pcDNA3中,构建出小鼠MIP-1α的真核表达质粒Pm;将其转染COS-7细胞,并用Boyden趋化小室法检测MIP-1α的生物学活性。然后用其与HSV-IIgD的DNA疫苗一起免疫BALB/c小鼠,检测免疫小鼠的特异性抗体、脾T细胞增殖反应及病毒攻击小鼠后对小鼠的保护率,观察MIP-1α对HSV-IIDNA疫苗免疫效果的影响。结果成功构建了小鼠MIP-1α的重组真核表达质粒;免疫BALB/c小鼠发现,其作为分子佐剂可加强HSV-IIgDDNA疫苗的免疫效果。结论小鼠MIP-1α可作为HSV-IIgDDNA疫苗的分子佐剂,为研制新型有效的HSV-IIDNA疫苗提供一定的依据。 展开更多
关键词 小鼠巨噬细胞炎性蛋白-1α(MIP-1α) 单纯疱疹病毒Ⅱ型(HSV-Ⅱ)dna疫苗 分子佐剂
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SPECIFIC IDENTIFICATION OF HERPES SIMPLEX VIRUS IN HUMAN ESOPHAGUS WITH RAPID IN SITU HYBRIDIZATION IN 5 CASES 被引量:1
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作者 Ying-lan Gao Sung-sun Kim +6 位作者 Chang-woo Han Yoo-duk Choi Jong-hee Nam Sang-woo Juhng Jun-shuo Jin Ling-fei Kong Chang-soo Park 《Chinese Medical Sciences Journal》 CAS CSCD 2008年第2期126-128,共3页
HUMAN herpes simplex virus esophagitis (HSVE) was first reported in 1940 by Johnson. ^1HSVE usually occurs in immunocompromised patients,such as those with acquired immunodeficiency syndrome (AIDS), 2-4 malignanc... HUMAN herpes simplex virus esophagitis (HSVE) was first reported in 1940 by Johnson. ^1HSVE usually occurs in immunocompromised patients,such as those with acquired immunodeficiency syndrome (AIDS), 2-4 malignancies, cutaneous burns, connective tissue diseases, inflammatory bowel disease, those taking immuno-suppressive therapy, and those undergoing organ transplantation,5 etc. In the immunocompetent individuals, HSVE is rare, having been reported in 39 cases and mainly affecting young males^6,7 The aim of this study was to delineate the clinical experience in the diagnosis of HSVE using rapid in situ hybridization and assess the various detection methods. 展开更多
关键词 herpes simplex virus ESOPHAGUS oligonucleotide dna probe in situ hybridization
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