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IMMUNOCHEMISTRY OF TYPE II GROUP B STREPTOCOCCI

IMMUNOCHEMISTRY OF TYPE II GROUP B STREPTOCOCCI
II 型 B 族链球菌的免疫化学
批准号:
3129394
负责人:
DAVID G PRITCHARD
金额:
$9.77万
依托单位国家:
美国
项目类别:
财政年份:
1983
资助国家:
美国
项目状态:
已结题
起止时间:
1983-05-01 至 1990-12-31

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中文摘要
翻译
II型B群链球菌是引起人类严重感染的常见原因
英文摘要
Type II group B Streptococci are a frequent cause of serious human infections. They are the major cause of maternal and adult group B streptococcal infections and are second only to type III strains as a cause of neonatal infections. Antibodies directed against the type-specific polysaccharides of group B streptococci are thought to play an important role in host defense against these organisms. However, the precise nature of the immunological determinants against which protective antibodies are directed is not understood. Therefore, the complete chemical structure of the type II polysaccharide will be determined using methylation analysis, specific chemical degradations and 13C-N.M.R. The exact nature of the importance immunological determinants will be defined using various oligosaccharide fragments as inhibitors in an ELISA employing monoclonal antibodies to the type II polysaccharide. In addition, the specificity of naturally occurring antibodies to type II group B streptococci will be examined in selected human sera from patients with known colonization status or infection. Two main antibody assays will be employed: a quantitative ELISA for measuring antibody levels, and an opsonophagocytic assay for assessing the functional role of these antibodies.
期刊论文(3)
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会议论文
DOI: 10.1016/0006-291x(87)91408-2
发表时间: 1987
期刊: Biochemical and biophysical research communications
影响因子: 3.1
作者: [Huang,DH, Pritchard,DG, Sakai,TT, Krishna,NR]
通讯作者: Krishna,NR
DOI: 10.1016/s0008-6215(00)90145-9
发表时间: 1986-11
期刊: Carbohydrate research
影响因子: 3.1
作者: [D. Huang;N. Krishna;D. Pritchard]
通讯作者: D. Huang;N. Krishna;D. Pritchard
B. anthracis Peptidoglycan Deacetylase as a Drug Target
Chemistry & Immunochemistry of Exosporium Carbohydrates
B. anthracis Peptidoglycan Deacetylase as a Drug Target
Inhibition of GBS Carriage by Engineered Lactobacilli
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