课题基金 / 基金详情

MONOCLONAL T LYMPHOCYTE FACTOR REGULATION OF MYELOMA

MONOCLONAL T LYMPHOCYTE FACTOR REGULATION OF MYELOMA
骨髓瘤的单克隆 T 淋巴细胞因子调节
批准号:
3173252
负责人:
JAMES W ROHRER
金额:
$13.01万
依托单位:
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

项目摘要

项目成果

JAMES W ROHRER的其他基金

相似基金

相关文献

中文摘要
翻译
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.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
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:
海外基金