IMMUNOLOGY OF CUTANEOUS BASOPHIL HYPERSENSITIVITY
皮肤嗜碱性粒细胞过敏的免疫学
基本信息
- 批准号:3480661
- 负责人:
- 金额:$ 38.61万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:1977
- 资助国家:美国
- 起止时间:1977-06-01 至 1992-05-31
- 项目状态:已结题
- 来源:
- 关键词:B lymphocyte T lymphocyte antibody receptor basophils cellular immunity complement delayed hypersensitivity electrofocusing guinea pigs histamine humoral immunity immunochemistry immunoglobulin E immunoglobulin G ion exchange chromatography laboratory mouse laboratory rat lymphokines macrophage mast cell radiotracer serology /serodiagnosis serotonin
项目摘要
Through study of cutaneous basophil hypersensitivity (CBH) it is now clear
that basophils and mast cells, their contained mediators (such as histamine
and serotonin), and their associated anaphylactic antibodies (IgE and
IgG1), are involved in delayed-time course reactions. These findings mean
that immune components improtant in allergic disease and astha are also
potentially important in immune resistance to microbes and parasites and in
rejection of tumors and tissue grafts. This research proposal submits a
comprehensive program for the continued investigation of the role of
antibodies in CBH responses of guinea pigs. We will study the mechanism by
which these antibodies mediate CBH by determining whether circulating
basophils, and basophils arriving at CBH reactions are sensitized with
antibodies that transfer CBH. We will also determine whether these
antibodies are a special subclass of IgG1 and whether lymphocytes or
macrophages are involved in the ability of antibodies to mediate CBH.
Finally, studies will be performed to determine whether these antibodies
are also involved in CBH reactions that are transferred by thymic-derived
lymphocytes (T cells). Studies will also be continued on the requirement
for T cells to activate mast cells to release the vasoactive amine
serotonin in murine delayed-type hypersensitivity (DTH). Serotonin
transport from mast cells in DTH, and in vitro will be studied. A mast
cell-derived serotonin protein that may be important in transport of
serotonin will be characterized. Finally, we will determine the mechanism
by which T cells may activate mast cells in DTH by determining whether
non-specific serotonin releasing lymphokines, or specific IgF-like factors
are involved.
通过对皮肤嗜碱性粒细胞超敏反应(CBH)的研究,
嗜碱性粒细胞和肥大细胞,它们所含的介质(如组胺
和血清素)及其相关的过敏性抗体(IgE和
IgG 1)参与延迟时间过程反应。 这些发现意味
过敏性疾病和哮喘中重要的免疫成分也
在对微生物和寄生虫的免疫抵抗中以及在
肿瘤和组织移植物的排斥反应。 本研究报告提出了一个
继续调查的作用的综合方案
豚鼠CBH反应中的抗体。 我们会研究有关机制,
这些抗体介导CBH通过确定是否循环
嗜碱性粒细胞和到达CBH反应的嗜碱性粒细胞被致敏,
转移CBH的抗体 我们还将确定这些
抗体是IgG 1的一个特殊亚类,无论是淋巴细胞还是
巨噬细胞参与抗体介导CBH的能力。
最后,将进行研究,以确定这些抗体是否
也参与CBH反应,通过胸腺衍生的
淋巴细胞(T细胞)。 还将继续研究
T细胞激活肥大细胞释放血管活性胺
血清素在小鼠迟发型超敏反应(DTH)中的作用。 血清素
从肥大细胞在DTH中的转运,并在体外进行研究。 桅杆
细胞衍生的5-羟色胺蛋白质,可能是重要的运输
5-羟色胺将被表征。 最后,我们将确定机制
通过确定T细胞是否可以激活DTH中的肥大细胞,
非特异性5-羟色胺释放淋巴因子或特异性IGF样因子
参与其中
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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PHILIP William ASKENASE其他文献
PHILIP William ASKENASE的其他文献
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{{ truncateString('PHILIP William ASKENASE', 18)}}的其他基金
Initiation of Contact and Asthmatic Hypersensitivity
接触的开始和哮喘过敏
- 批准号:
7183609 - 财政年份:2004
- 资助金额:
$ 38.61万 - 项目类别:
Initiation of Contact and Asthmatic Hypersensitivity
接触的开始和哮喘过敏
- 批准号:
7023890 - 财政年份:2004
- 资助金额:
$ 38.61万 - 项目类别:
Initiation of Contact and Asthmatic Hypersensitivity
接触的开始和哮喘过敏
- 批准号:
7367191 - 财政年份:2004
- 资助金额:
$ 38.61万 - 项目类别:
Initiation of Contact and Asthmatic Hypersensitivity
接触的开始和哮喘过敏
- 批准号:
6861027 - 财政年份:2004
- 资助金额:
$ 38.61万 - 项目类别:
Initiation of Contact and Asthmatic Hypersensitivity
接触的开始和哮喘过敏
- 批准号:
6759076 - 财政年份:2004
- 资助金额:
$ 38.61万 - 项目类别:
INITIATOR T CELLS IN DELAYED-TYPE HYPERSENSITIVITY
迟发型超敏反应中的启动 T 细胞
- 批准号:
3140567 - 财政年份:1989
- 资助金额:
$ 38.61万 - 项目类别:
INITIATOR CELLS IN DELAYED-TYPE HYPERSENSITIVITY
迟发型超敏反应的起始细胞
- 批准号:
2063492 - 财政年份:1989
- 资助金额:
$ 38.61万 - 项目类别:
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