INDUCTION OF ALLOGRAFT TOLERANCE
INDUCTION OF ALLOGRAFT TOLERANCE
批准号:
2390225
负责人:
CHRISTENE A HUANG
金额:
$2.44万
依托单位国家:
美国
项目类别:
财政年份:
1997
资助国家:
美国
项目状态:
未结题
起止时间:
1997-04-01 至
关键词:
Primates biomarker bone marrow transplantation cellular immunity disease /disorder model histocompatibility typing homologous transplantation immune tolerance /unresponsiveness immunocytochemistry immunogenetics kidney transplantation messenger RNA polymerase chain reaction tissue /cell culture transplantation immunology
中文摘要
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英文摘要
This proposal is designed to study the mechanism of donor specific
allograft tolerance induced through mixed allogeneic bone marrow chimerism
in the clinically relevant monkey model. The specific aims of this
project include determining what particular cells from the donor bone
marrow are necessary to establish immunological tolerance and whether or
not long-term chimerism is necessary to maintain tolerance to the
allograft. In tolerant animals whose donor derived cells are undetectable
in the peripheral blood, lymphoid tissues will be extensively examined for
evidence of chimerism. The role of the allograft itself in the
maintenance of long-term immunological tolerance will also be studied.
Donor bone marrow will be fractionated using magnetic bead separation of
cells labeled with mAbs to particular cell lineage markers. The
particular bone marrow cell subsets will be transferred into MHC
mismatched recipients which have been subjected to the non-lethal
preparative regimen to allow for bone marrow engraftment and establishment
of mixed chimerism. Lymphoid tissues will then be examined by
immunohistochemistry and by PCR to detect donor derived cell lineages at
sequential times after bone marrow transfer. Irradiated bone marrow will
be transferred at the time of kidney transplant to determine whether the
donor bone marrow acts passively as a source of antigen rather than
actively in the establishment of tolerance. These studies will have
important implications for the understanding of tolerance in primates and
may ultimately lead to establishment of clinical protocols to prevent
organ transplant rejection across allogeneic barriers without the need for
chronic immunosuppression.
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