Immunoprofiling of older persons
Immunoprofiling of older persons
批准号:
6884349
负责人:
Andrzej K Drukier
金额:
$9.98万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2005
资助国家:
美国
项目状态:
已结题
起止时间:
2005-09-01 至 2006-02-28
关键词:
beta antiadrenergic agentbiomarkercardiovascular disorderclinical researchcytokinediagnosis design /evaluationdiagnosis quality /standardenzyme linked immunosorbent assayfemalehuman middle age (35-64)human old age (65+)human tissueimmune responseimmunologic assay /testinflammationinterferon gammainterleukin 1interleukin 10interleukin 11interleukin 18interleukin 4interleukin 6interleukin 8protein quantitation /detectiontumor necrosis factor alphawomen&aposs health
中文摘要
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英文摘要
DESCRIPTION (provided by applicant):
Abstract: Autoimmune diseases and older people with weakened immune system are a major public health problem; for example, there are about 2 million individuals with RA, i.e. about 1 % of population of USA. Similarly, there are millions of older people with cardiovascular diseases. Better information is needed about the immunoprofiles of older persons.
The specific aims of the proposed Phase I studies are to study the age dependent changes in two cohorts of older women: healthy and with cardiac problems. The last group will be divided into two sub-groups: those treated with beta blockers and those not treated. More specifically, the aims are:
Aim 1: Develop the supersensitive panel of assays targeting cytokines in older persons; i.e. further improve immunoassays for pro-inflammatory cytokines (TNF-alpha, IFN-gamma, IL-1 beta and IL-6) and anti-inflammatory cytokines (IL-4, IL-10, IL-11);
Aim 2: Develop the super-sensitive assay for IL-8 and IL-18;
Aim 3: Study the differences in immunoprofiles between women who are healthy and who have cardiac disorders.
Phase II will continue the clinical validation of assays developed in the Phase I effort, e.g. we will develop supersensitive assays targeting five additional cytokines. MPD enhanced P-chips (P-chips/MPD) will be used to measure all relevant biomarkers concurrently in a low cost, supersensitive modality. We will optimize the sensitivity, accuracy and user-friendliness of the P-chip/MPD. Concurrent quantitation of cytokines and other low level biomarkers will permit studies of correlation between the immune system and cardiac output.
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