ROLE OF CTLA 4 IN IMMUNE TOLERANCE IN HUMANS
CTLA 4 在人类免疫耐受中的作用
基本信息
- 批准号:6633680
- 负责人:
- 金额:$ 26.27万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2001
- 资助国家:美国
- 起止时间:2001-03-01 至 2005-02-28
- 项目状态:已结题
- 来源:
- 关键词:CD28 molecule CD3 molecule SCID mouse T lymphocyte acid phosphatase cyclins immune tolerance /unresponsiveness interleukin 2 membrane proteins mitogen activated protein kinase mixed tissue /cell culture neoplasm /cancer immunology neoplasm /cancer immunotherapy neutralizing antibody nonhuman therapy evaluation proliferating cell nuclear antigen prostate neoplasms surface antigens tumor antigens
项目摘要
DESCRIPTION: (Adapted from applicant's abstract) CTLA-4, a transmembrane
protein expressed transiently on activated T cells, downregulates T cell
activation and promotes tolerance in experimental animals. However, neither the
molecular basis for these effects nor the extent to which CTLA-4 influences the
human immune system are known. Our preliminary findings indicate that CTLA-4
triggering blocks cell cycle progression and promotes anergy in human CD4+ T
cells, in vitro. The goals of this project are to define the molecular basis
for these effects and determine if CTLA-4 plays a role in regulating human T
cell responses, in vivo. Four specific aims are proposed: 1) to determine the
function of CTLA-4 in the induction and maintenance of anergy in adult human T
cells; 2) to define the molecular basis for CTLA-4 signalling by introducing
into human T cells selected mutant forms of CTLA-4 and a variety of signalling
intermediates; 3) to determine the role of CTLA-4 in regulating the immune
response to self and non-self antigens, in vivo, in immunocompetent SCID/Hu
mice; and 4) to determine if administration of anti-CTLA-4 antibody can reverse
tolerance to a tumor associated antigen, in vivo, under conditions that mimic
those in human cancer. The results of these studies should not only allow us to
determine if and how CTLA-4 affects tolerance induction and maintenance in
humans but potentially provide the basis for an effective immunotherapeutic
approach to cancer.
描述:(改编自申请人摘要)CTLA-4,一种跨膜
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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EDGAR G. ENGLEMAN其他文献
EDGAR G. ENGLEMAN的其他文献
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{{ truncateString('EDGAR G. ENGLEMAN', 18)}}的其他基金
Systems Biology of Tumor-Immune-Stromal Interactions in Metastatic Progression
转移进展中肿瘤-免疫-基质相互作用的系统生物学
- 批准号:
10729464 - 财政年份:2023
- 资助金额:
$ 26.27万 - 项目类别:
Project 3: Impact of tumor genetics on PDAC immunobiology and responses to macrophage-targeted immunotherapy
项目 3:肿瘤遗传学对 PDAC 免疫生物学的影响以及对巨噬细胞靶向免疫治疗的反应
- 批准号:
10704089 - 财政年份:2021
- 资助金额:
$ 26.27万 - 项目类别:
Targeting Lymph Node Dependent Immune Tolerance in Cancer
针对癌症中的淋巴结依赖性免疫耐受
- 批准号:
10210557 - 财政年份:2021
- 资助金额:
$ 26.27万 - 项目类别:
Innate Immune Mechanisms Contributing to Cancer Growth in Obesity
肥胖导致癌症生长的先天免疫机制
- 批准号:
10654802 - 财政年份:2021
- 资助金额:
$ 26.27万 - 项目类别:
Innate Immune Mechanisms Contributing to Cancer Growth in Obesity
肥胖导致癌症生长的先天免疫机制
- 批准号:
10430268 - 财政年份:2021
- 资助金额:
$ 26.27万 - 项目类别:
Innate Immune Mechanisms Contributing to Cancer Growth in Obesity
肥胖导致癌症生长的先天免疫机制
- 批准号:
10278250 - 财政年份:2021
- 资助金额:
$ 26.27万 - 项目类别:
Project 3: Impact of tumor genetics on PDAC immunobiology and responses to macrophage-targeted immunotherapy
项目 3:肿瘤遗传学对 PDAC 免疫生物学的影响以及巨噬细胞靶向免疫治疗的反应
- 批准号:
10456771 - 财政年份:2021
- 资助金额:
$ 26.27万 - 项目类别:
Innate Immune Mechanisms Contributing to Cancer Growth in Obesity
肥胖导致癌症生长的先天免疫机制
- 批准号:
10706825 - 财政年份:2021
- 资助金额:
$ 26.27万 - 项目类别:
Project 3: Impact of tumor genetics on PDAC immunobiology and responses to macrophage-targeted immunotherapy
项目 3:肿瘤遗传学对 PDAC 免疫生物学的影响以及对巨噬细胞靶向免疫治疗的反应
- 批准号:
10187127 - 财政年份:2021
- 资助金额:
$ 26.27万 - 项目类别:
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