Mechanisms ot Maternal Immune Tolerence
Mechanisms ot Maternal Immune Tolerence
批准号:
6619506
负责人:
LAURIE Hollis GLIMCHER
金额:
$40.5万
依托单位国家:
美国
项目类别:
财政年份:
2002
资助国家:
美国
项目状态:
已结题
起止时间:
2002-08-01 至 2007-05-31
关键词:
antigen presenting cell cytotoxic T lymphocyte dendritic cells genetically modified animals helper T lymphocyte hormone regulation /control mechanism immune tolerance /unresponsiveness laboratory mouse leukocyte activation /transformation ovalbumin placenta pregnancy immunology tissue /cell culture trophoblast uterus
中文摘要
描述(由申请人提供):异体胎儿如何避免母体
英文摘要
Description (provided by applicant): How the allogeneic fetus avoids maternal
immune rejection during pregnancy is not only one of the outstanding questions
in contemporary immunology, but is also now recognized to have major clinical
relevance towards diseases such as recurrent spontaneous abortion and
preeclampsia, as well as application towards organ transplantation. Although
it is generally accepted that the maternal immune system is ?aware? that the
fetus and placenta exist, studies to date have only focused on CD8+ T cells
and B cells, and thus have not addressed the behavior of potentially reactive
CD4+ T helper cells, the lymphocyte subset likely to play the most important
role in any form of antigen-specific tolerance induction. Here, we will
directly characterize the responses of both maternal CD4+ and CD8+ T cells
towards a placentally expressed antigen, taking advantage of transgenic mice
we have recently made that express the well-characterized model antigen
ovalbumin in placental tissues (Aim 1). The use of this system will also allow
us to test whether maternal tolerance towards the fetus and placenta is local
or systemic, and whether it involves attenuation of affector or effector arms
of the immune response. The nature of antigen presenting cells (APCs) in the
pregnant uterus is another area that is virtually unexplored, despite the
central role of these cells in regulating tolerance induction. Thus, we will
characterize the behavior and antigen-presenting capacity of APCs in the
pregnant uterus, focusing on resident dendritic cells, which have been
completely uncharacterized in mice (Aim 2). Lastly, we describe the generation
of novel transformed murine trophoblast cell lines directly from cultured
trophoblast stem cells. Since these transformed trophoblasts are rejected in
non-pregnant allogeneic mice following subcutaneous injection, they provide a
powerful reagent for dissecting the relative importance of trophoblasts, the
uterine environment, and the hormonal state of pregnancy in establishing
maternal tolerance (Aim 3).
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海外基金