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BIOLOGICAL STUDIES OF HUMAN INTERLEUKIN I

BIOLOGICAL STUDIES OF HUMAN INTERLEUKIN I
人白细胞介素 I 的生物学研究
批准号:
3176050
负责人:
Lawrence B Lachman
金额:
$9.02万
依托单位国家:
美国
项目类别:
财政年份:
1984
资助国家:
美国
项目状态:
已结题
起止时间:
1984-07-01 至 1987-06-30

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中文摘要
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英文摘要
The role of monocytes and macrophages in inflammatory and immune responses has yet to be characterized at the molecular level. Although it is clear that activated macrophages an monocytes release a large number of biological mediators at the site of inflammation, the effect of these mediators upon lymphocytes, fibroblasts, endothelial and possibly other cells remains to be determined. A single pluripotent monokine, Interleukin 1 (IL 1), has been demonstrated to affect the inflammatory process at several stages. Although Interleukin 1 has been extensively investigated, it has not been purified to homogeneity in a biologically active form. In addition, monoclonal antibodies to IL 1, which are required to measure IL 1 in biological fluids, to affinity purify IL 1, and to isolate polysomal mRNA for gene cloning, have yet to be developed. Once the primary sequence of IL 1 has been determined, it will be possible to predict antigenic regions to select possible sequences for nuceotide probes specific for IL 1 coding m RNA, and to indicate possible amino acid sequences for antagonists of IL 1 which may be potential anti-inflammatory and anti arthritic agents. It is proposed to determine the primary structure of human IL 1 purified to homogeneity by SDS-polyacrylamide gel electrophoresis. (2) To prepare homogeneously purified human IL 1 which retains biological activity. (3) To prepare monoclonal antibodies and heteranisera to human IL 1. (4) To use the abovementioned antibodies to develop ELISA assays which can quantitate IL 1 levels in complex bodily fluids, and to prepare affinity reagents which can remove IL 1 from these fluids. (5) To continue biological studies using homogeneously purified, biologically active IL 1 to unequivocally establish that a single molecule elevates fever, induces fibroblast proliferation stimulates collagenase release from fibroblasts, stimulates acute phase reactants when injected in vivo, induces B and T lymphocyte proliferation and granulopoeisis, and possibly affects vascular permeability.
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