IMMUNOTOXIC EFFECTS OF IODINE
碘的免疫毒性作用
基本信息
- 批准号:3243232
- 负责人:
- 金额:$ 10.62万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:1992
- 资助国家:美国
- 起止时间:1992-04-01 至 1995-03-31
- 项目状态:已结题
- 来源:
- 关键词:SDS polyacrylamide gel electrophoresis T lymphocyte autoantibody autoimmune thyroiditis cellular immunity enzyme linked immunosorbent assay high performance liquid chromatography human subject immunotoxicity interleukin 2 interleukin 4 iodine laboratory mouse monoclonal antibody thyroglobulin tissue /cell culture western blottings
项目摘要
Increased environmental exposure to iodine from dietary or therapeutic
sources may contribute to the escalating prevalence of autoimmune
thyroiditis in humans. Highly iodinated thyroglobulin, the 660 Kd
glycoprotein major storage form of thyroid hormones, due to increased
iodine intake, has been associated with increased incidence and severity
of spontaneous autoimmune thyroiditis in chickens and in the diabetes-
prone lymphocytic thyroiditis-associated BB/W rat. Clinical observations
in humans also associate excess iodine as a potentiator of autoimmune
thyroid disease, but no experimental information about the pathogenesis
in humans is available. The role of iodine in a multifactorial
autoimmune disease like chronic lymphocytic thyroiditis is a factor that
has too frequently been neglected and may account for many of the
differences in frequency of autoimmune thyroid disease among
geographical areas. We propose to explore the differences in the immune
response to thyroglobulin and its fragments iodinated to varying degrees
between patients suffering from autoimmune thyroid disease compared to
euthyroid individuals with thyroid autoantibodies. First, studies will
concentrate on the preparation, iodination, isolation, and
identification of the relevant thyroglobulin and its fragments. Tryptic-
digest peptide maps resolved by HPLC will enable us to compare patterns
of iodination among the various Tg preparations. Second, we propose, to
evaluate cellular human immune response to variously iodinated
thyroglobulin or its fragments. The functional responses of human
lymphocytes to variously iodinated thyroglobulin and its fragments will
be tested by means of cell proliferation assays. We will develop a
series of T cell lines/clones to test the fine specificities of the
cellular response. We will then investigate markers of cellular
proliferation (e.g. IL-2, IL-4 secretion) to pinpoint the specific stage
at which the thyroglobulin or its fragments is playing a role. The
ultimate goal is to understand the immunotoxic role of iodine in
inducing autoimmune thyroid disease with the hope of developing
preventive strategies.
从饮食或治疗中摄入碘的环境暴露增加
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)
数据更新时间:{{ journalArticles.updateTime }}
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
数据更新时间:{{ journalArticles.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ monograph.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ sciAawards.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ conferencePapers.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ patent.updateTime }}
Carol Lynne Burek其他文献
Carol Lynne Burek的其他文献
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
{{ truncateString('Carol Lynne Burek', 18)}}的其他基金
NOD-H2H4 MICE AS A SENTINEL MODEL FOR AUTOIMMUNE THYROID
NOD-H2H4 小鼠作为自身免疫性甲状腺的哨兵模型
- 批准号:
6382344 - 财政年份:1999
- 资助金额:
$ 10.62万 - 项目类别:
NOD-H2H4 MICE AS A SENTINEL MODEL FOR AUTOIMMUNE THYROID
NOD-H2H4 小鼠作为自身免疫性甲状腺的哨兵模型
- 批准号:
6178201 - 财政年份:1999
- 资助金额:
$ 10.62万 - 项目类别:
NOD H2H4 MICE AS A SENTINEL MODEL FOR AUTOIMMUNE THYROID
NOD H2H4 小鼠作为自身免疫性甲状腺的哨兵模型
- 批准号:
6078591 - 财政年份:1999
- 资助金额:
$ 10.62万 - 项目类别:
相似海外基金
Modulation of T lymphocyte Activation by Ã2-Adrenergic Receptor Signalling Pathways
α2-肾上腺素能受体信号通路对 T 淋巴细胞激活的调节
- 批准号:
RGPIN-2019-06980 - 财政年份:2022
- 资助金额:
$ 10.62万 - 项目类别:
Discovery Grants Program - Individual
A precision tumor neoantigen identification pipeline for cytotoxic T-lymphocyte-based cancer immunotherapies
用于基于细胞毒性 T 淋巴细胞的癌症免疫疗法的精准肿瘤新抗原识别流程
- 批准号:
10581488 - 财政年份:2022
- 资助金额:
$ 10.62万 - 项目类别:
Modulation of T lymphocyte Activation by ß2-adrenergic Receptor Signalling Pathways
α2-肾上腺素能受体信号通路对 T 淋巴细胞激活的调节
- 批准号:
574979-2022 - 财政年份:2022
- 资助金额:
$ 10.62万 - 项目类别:
University Undergraduate Student Research Awards
A precision tumor neoantigen identification pipeline for cytotoxic T-lymphocyte-based cancer immunotherapies
用于基于细胞毒性 T 淋巴细胞的癌症免疫疗法的精准肿瘤新抗原识别流程
- 批准号:
10332251 - 财政年份:2022
- 资助金额:
$ 10.62万 - 项目类别:
Modulation of T lymphocyte Activation by Ã2-adrenergic Receptor Signalling Pathways
α2-肾上腺素能受体信号通路对 T 淋巴细胞激活的调节
- 批准号:
574984-2022 - 财政年份:2022
- 资助金额:
$ 10.62万 - 项目类别:
University Undergraduate Student Research Awards
Modulation of T lymphocyte Activation by ß2-adrenergic Receptor Signalling Pathways
α2-肾上腺素能受体信号通路对 T 淋巴细胞激活的调节
- 批准号:
574985-2022 - 财政年份:2022
- 资助金额:
$ 10.62万 - 项目类别:
University Undergraduate Student Research Awards
Modulation of T lymphocyte Activation by Ã2-adrenergic Receptor Signalling Pathways
α2-肾上腺素能受体信号通路对 T 淋巴细胞激活的调节
- 批准号:
574978-2022 - 财政年份:2022
- 资助金额:
$ 10.62万 - 项目类别:
University Undergraduate Student Research Awards
Investigating the cell-based activity of a new class of cytotoxic T-lymphocyte antigen-4 (CTLA-4) small molecule inhibitors
研究一类新型细胞毒性 T 淋巴细胞抗原 4 (CTLA-4) 小分子抑制剂的细胞活性
- 批准号:
444149 - 财政年份:2021
- 资助金额:
$ 10.62万 - 项目类别:
Operating Grants
Novel pathways in T lymphocyte differentiation and function
T 淋巴细胞分化和功能的新途径
- 批准号:
RGPIN-2015-05491 - 财政年份:2021
- 资助金额:
$ 10.62万 - 项目类别:
Discovery Grants Program - Individual
Modulation of T lymphocyte Activation by ß2-Adrenergic Receptor Signalling Pathways
通过 α2-肾上腺素能受体信号通路调节 T 淋巴细胞激活
- 批准号:
RGPIN-2019-06980 - 财政年份:2021
- 资助金额:
$ 10.62万 - 项目类别:
Discovery Grants Program - Individual