RISK OF PORCINE PICORNAVIRUS IN XENOTRANSPLATATION
RISK OF PORCINE PICORNAVIRUS IN XENOTRANSPLATATION
批准号:
6526575
负责人:
M KARIUKI NJENGA
金额:
$14.2万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2000
资助国家:
美国
项目状态:
已结题
起止时间:
2000-09-01 至 2004-08-31
关键词:
Picornaviridae SCID mouse communicable disease transmission density gradient ultracentrifugation disease /disorder model disease /disorder proneness /risk electron microscopy encephalomyocarditis virus epizootiology heart transplantation human tissue immunosuppression in situ hybridization laboratory rabbit light microscopy organ culture pancreas transplantation polymerase chain reaction southern blotting swine virus infection mechanism virus replication western blottings xenotransplantation zoonosis
中文摘要
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英文摘要
DESCRIPTION
(Adapted from applicant's abstract) This research career award is designed to
provide the candidate with research experience in xenotransplantation biology
and porcine animal model of infectious diseases, with the long-term objective
of establishing a research program in xenozoonosis. The candidate has
research experience in cellular and molecular virology and the mouse animal
model and he has recently taken a faculty position at the University of
Minnesota, which is renowned for research in the fields of transplantation and
pig diseases. The research project will investigate the risk posed by
persistent porcine viruses, which may escape detection by standard screening
methods to become pathogenic in humans following xenotransplatation. The
experiments will utilize porcine encephalomyocarditis virus (EMCV), which has
been shown to cause-species infection, to evaluate the risk of human infection
after transplantation of pig tissues by examining various pigs tissues/organs
using sensitive molecular techniques to determine where the virus persists.
Subsequently, the applicants will transplant chronically EMCV-infected porcine
tissues into SCID (severe combined immunodeficient) mice reconstituted with
human peripheral blood lymphocytes followed by immunosuppressive treatment
(hu-PBL-ISCID), in order to determine the risk of such tissues transmitting
disease. The hu-PBL-ISCID mice will serve as a model of suppressed immune
system in transplant patients. This training program will also require the
candidate to observe and assist in monkey-to-monkey (allo-) and pig-to-monkey
(xeno-) transplantations in an established transplantation laboratory. The
long-term goal is to transplant pig organs/tissues containing persistent
porcine virus into primates in order to determine the risk of disease.
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会议论文
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