REGULATORY MECHANISMS IN THE IMMUNE RESPONSE
REGULATORY MECHANISMS IN THE IMMUNE RESPONSE
批准号:
3480905
负责人:
JOHN W KAPPLER
金额:
$11.33万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
1979
资助国家:
美国
项目状态:
已结题
起止时间:
1979-12-01 至 1991-11-30
关键词:
B lymphocyte T cell receptor T lymphocyte affinity chromatography antigens antireceptor antibody autoradiography biological signal transduction cell cell interaction cellular immunity concanavalin A flow cytometry gel electrophoresis genetically modified animals helper T lymphocyte high performance liquid chromatography hybridomas immunoglobulin M immunoregulation interferons interleukin 1 interleukin 2 laboratory mouse laboratory rat leukocyte activation /transformation liposomes lymphokines major histocompatibility complex membrane activity membrane proteins monoclonal antibody neoplastic cell culture for noncancer research tissue /cell culture
中文摘要
这项建议的目的是详细了解
T细胞帮助B细胞对抗原做出反应。我们是
对发生的两个过程特别感兴趣;第一,
启动B细胞反应的事件,其次,对
淋巴因子B细胞刺激因子-1(BSF1)。
尽管淋巴因子本身可以驱动B细胞对
B细胞对多种抗原的某些抗原反应,尤其是
那些出生在蛋白质上的人,需要携带者特异性T细胞的存在
细胞和淋巴因子。这些T细胞似乎参与了
主要是在B细胞反应的开始阶段。他们可能是
通过分泌一些迄今未被发现的淋巴因子或通过
它们自己的膜蛋白与T上的配体直接接触
或B细胞和/或分离的膜蛋白,我们计划
调查以下哪种可能性是正确的。膜
要研究的成分包括T细胞受体,L3T4,
LFA-1和II类分子。例如,我们将隔离
来自特定辅助T细胞杂交瘤的受体并通过
这些受体是否与抗原+结合的各种策略
MHC。这些受体将用于脂质体或在此之后
转移到另一个T细胞杂交瘤进行抗原特异性检测
帮助者活动。
BSF1对B细胞有多种影响。它诱导Ia合成
在静息细胞中,并刺激亚最大增殖
激活的B细胞。我们计划分离B细胞上BSF1的受体
细胞,并详细研究这种淋巴因子的诱导作用。
没有休眠细胞。
英文摘要
The aims of this proposal are to understand in detail the means
whereby T cells help B cells respond to antigen. We are
particularly interested in two processes which occur; first, the
events which initiate B cell response and secondly, the effects on
B cells of the lymphokine B cell stimulating factor-1 (BSF1).
Although lymphokines alone can drive the responses of B cells to
some antigens responses of B cells to many antigens, particularly
those born on proteins, require the presence of carrier-specific T
cells as well as lymphokines. These T cells appear to be involved
chiefly at the beginning of the B cell response. they may be
acting by secreting some hitherto undiscovered lymphokine or by
direct contact of their own membrane proteins with ligands on T
or B cells and/or isolated membrane proteins, we plan to
investigate which of these possibilities is correct. Membrane
components to be studied will include the T cell receptor, L3T4,
LFA-1 and Class II molecules. For example, we will isolate
receptors from a particular helper T cell hybridoma and test by
various strategies whether these receptors bind antigen plus
MHC. These receptors will be used in liposomes or after
transfer to another T cell hybridoma to test for antigen-specific
helper activity.
BSF1 has a number of effects on B cells. It induces Ia synthesis
in resting cells, and stimulates proliferation of sub-maximally
activated B cells. We plan to isolate the receptor for BSF1 on B
cells, and study in detail the inductive effects of this lymphokine
no resting cells.
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