MURINE AIDS MODEL: C PARVUM PROBIOTICS, OPPORTUNISTIC INFEC: MAIDS: TCR GENE:
MURINE AIDS MODEL: C PARVUM PROBIOTICS, OPPORTUNISTIC INFEC: MAIDS: TCR GENE:
批准号:
6506355
负责人:
JOHN I ALAK
金额:
$11.63万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2001
资助国家:
美国
项目状态:
已结题
起止时间:
2001-06-01 至 2002-05-31
中文摘要
本提案的总体目标是研究
英文摘要
The overall objective of this proposal is to study the
host/pathogen interaction at mucosal surfaces and to develop
prevention strategies that maximize protective mucosal immune
responses to Cryptosporidiumum parvum (C parvum). We will develop and
maintain a murine model for murine acquired immunodeficiency syndrome
(MAIDS) which will be used to study the pathogenesis of C parmm; a
potential pathogen commonly associated with AIDS. To develop the
MAIDS model, C57BI_16 female mice win be immunosuppressed by
inoculation with LP-BM5; then challenged with C parvum 3 months post
LP-BM5 infection. Studies of experimentally induced cryptosporidiosis
using this model, will serve as a relevant tool for evaluating various
therapies for prevention of this opportunistic disease as our previous
studies have confirmed that mice infected with LP-BM5, develop
persistent experimental cryptosporidiosis with high numbers of oocysts
shed in the feces. Since the spread of AIDS is global and frequently
assoc iated with opportunistic infections including cryptosporidiosis,
it is critical to control AIDS-related o0portunistic diseases to
alleviate human suffering in order to minimize both social and
economic impact on society. Our long range goal will be to develop
effective prophylactic regimens for the control of Cryptosporidium.
infection, especially through nutritional, immunotherapeutic or
chemotherapeutic interventions. As yet, no effective treatment for
cryptosporidiosis has been reported. We will achieve the following
specific aims during these studies: elucidate the role of cellular
gut immunity to C parvum in this MAIDS model by determining the roles
and phenotypic frequencies of intestinal (1) intraepithelial (EEL's)
and (2) lamina propria (LPL) subpopulations (CD4', CD8, IgA, IgG' and
IgM') and cytokine (TNF-a , IFN-y, IL-1, IL-2, 4, 5 and 10) production
post C parvum challenge. (3) evaluate the efficacy of Lactobacillus
reuteri and L. acidophilus as probiotics for the control of
cryptosporidiosis and (4) evaluate the efficacy of probiotics and (5)
vavvines administered simultaneously for the control of
cryptosporidiosis. Results obtained from these studies will be
relevant in the development of new therapies for the control of
cryptosporidiosis and other opportunistic diseases in immuncompromised
individuals especially AIDS subjects.
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会议论文
MURINE AIDS MODEL: C PARVUM PROBIOTICS, OPPORTUNISTIC INFEC: MAIDS: TCR GENE:
-
批准号:6604785
-
项目类别:
-
资助金额:$11.63万
-
财政年份:2002
-
负责人:JOHN I ALAK
-
依托单位:
MURINE AIDS MODEL: C PARVUM PROBIOTICS, OPPORTUNISTIC INFEC: MAIDS: TCR GENE:
-
批准号:6593140
-
项目类别:
-
资助金额:$11.63万
-
财政年份:2001
-
负责人:JOHN I ALAK
-
依托单位:
MURINE AIDS MODEL: C PARVUM PROBIOTICS, OPPORTUNISTIC INFEC: MAIDS: TCR GENE:
-
批准号:6475068
-
项目类别:
-
资助金额:$3.95万
-
财政年份:2001
-
负责人:JOHN I ALAK
-
依托单位:
MURINE AIDS MODEL: C PARVUM PROBIOTICS, OPPORTUNISTIC INFEC: MAIDS: TCR GENE:
-
批准号:6326184
-
项目类别:
-
资助金额:$11.79万
-
财政年份:2000
-
负责人:JOHN I ALAK
-
依托单位:
MURINE AIDS MODEL: C PARVUM PROBIOTICS, OPPORTUNISTIC INFEC: MAIDS: TCR GENE:
-
批准号:6348005
-
项目类别:
-
资助金额:$3.95万
-
财政年份:2000
-
负责人:JOHN I ALAK
-
依托单位:
MURINE AIDS MODEL: C PARVUM PROBIOTICS, OPPORTUNISTIC INFEC: MAIDS: TCR GENE:
-
批准号:6121526
-
项目类别:
-
资助金额:$11.79万
-
财政年份:1999
-
负责人:JOHN I ALAK
-
依托单位:
海外基金