MONOCLONAL T LYMPHOCYTE FACTOR REGULATION OF MYELOMA
MONOCLONAL T LYMPHOCYTE FACTOR REGULATION OF MYELOMA
批准号:
3173252
负责人:
JAMES W ROHRER
金额:
$13.01万
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:
1984-04-01 至 1990-03-31
关键词:
T cell receptor affinity chromatography cell growth regulation clone cells erythrocytes gel electrophoresis helper T lymphocyte immune adherence reaction immunochemistry immunoglobulin A immunoglobulin idiotypes immunologic techniques immunomodulators immunoregulation laboratory mouse leukocyte activation /transformation lymphokines macrophage major histocompatibility complex multiple myeloma neoplasm /cancer immunotherapy secretory immune system suppressor T lymphocyte
中文摘要
MOPC-315是一种抗tnp分泌iga的BALB/c浆细胞瘤
英文摘要
MOPC-315 is an anti-TNP IgA-secreting BALB/c plasmacytoma
which is composed of lymphocytoid, non-secretory cells, IgA 315-
secreting plasmacytoid cells, and intermediate cells. During in
vivo growth the lymphocytoid, non-secretory 315 cells proliferate
and differentiate into the IgA 315-secreting plasmacytoid cells.
That growth and differentiation can be regulated in vivo and in
vitro by carrier-specific helper, suppressor, and contrasuppressor
T cells. Some of the differentiation regulating T cells specifically
recognize not only carrier antigen but also IgA 315 idiotopes. The
experiments described herein involve production and
characterization of monoclonal T cell lines from sheep
erythrocyte (SRBC)-immune BALB/c mice which can enhance,
suppress, or contrasuppress the growth or secretory
differentiation of MOPC-315 cells in vitro. Since in vivo and in
vitro experiments suggest that regulation is occurring due to T
cell release of soluble regulatory factors, this grant also is
focused on purification, and biochemical and serological
characterization of the regulatory factors. This is particularly
important since all of the regulatory cells appear to act on the
non-secretory lymphocytoid population of MOPC-315 and appear
to interact with the cells through either surface IgA 315 idiotopes
or through surface IgA 315 binding TNP-SRBC. Thus, information
about structure-function relationships of these factors is possible
to obtain. Idiotype 315-specific differentiation helper T (THd)
cell, SRBC-specific differentiation suppressor T (Tsd) cell, and
idiotype 315-specific differentiation contrasuppressor T (TCSd)
cell monoclonal lines have already been produced. Polyclonal THd
cells can protect mice against MOPC-315 tumor growth by
apparently reducing the cells proliferative potential by inducing
its differentiation. Experiments designed to determine the
mechanism by which THd cells can inhibit tumor progression in
mice and efficacy of using purified idiotype 315- and SRBC-
specific THd helper factors as therapeutic drugs against MOPC-
315 cells in vivo are described herein. These experiments may
demonstrate that regulatory stimuli as well as cytotoxic
intervention can have therapeutic effects on some tumors'
progression.
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MONOCLONAL T LYMPHOCYTE FACTOR REGULATION OF MYELOMA
-
批准号:3173251
-
项目类别:
-
资助金额:$12.81万
-
财政年份:1984
-
负责人:JAMES W ROHRER
-
依托单位:
MONOCLONAL T LYMPHOCYTE FACTOR REGULATION OF MYELOMA
-
批准号:3173249
-
项目类别:
-
资助金额:$9.33万
-
财政年份:1984
-
负责人:JAMES W ROHRER
-
依托单位:
MONOCLONAL T LYMPHOCYTE FACTOR REGULATION OF MYELOMA
-
批准号:3173247
-
项目类别:
-
资助金额:$13.59万
-
财政年份:1984
-
负责人:JAMES W ROHRER
-
依托单位:
MONOCLONAL T LYMPHOCYTE FACTOR REGULATION OF MYELOMA
-
批准号:3173250
-
项目类别:
-
资助金额:$9.49万
-
财政年份:1984
-
负责人:JAMES W ROHRER
-
依托单位:
IMMUNOREGULATION OF MYELOMA CELL DIFFERENTIATION
-
批准号:3168293
-
项目类别:
-
资助金额:$8.78万
-
财政年份:1980
-
负责人:JAMES W ROHRER
-
依托单位:
IMMUNOREGULATION OF MYELOMA CELL DIFFERENTIATION
-
批准号:3168294
-
项目类别:
-
资助金额:$8.94万
-
财政年份:1980
-
负责人:JAMES W ROHRER
-
依托单位:
海外基金