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HOST LYMPHOCYTE RESISTANCE TO HIV1

HOST LYMPHOCYTE RESISTANCE TO HIV1
宿主淋巴细胞对 HIV1 的抵抗力
批准号:
6169290
负责人:
Miles W. Cloyd
金额:
$25.68万
依托单位国家:
美国
项目类别:
财政年份:
1995
资助国家:
美国
项目状态:
已结题
起止时间:
1995-09-15 至 2002-06-30

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中文摘要
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英文摘要
DESCRIPTION (adapted from the Abstract): This is project to continue the study of host genetic resistance to HIV-1. The project evolved from early studies which showed that CD4 lymphocytes from random individuals possessed differential susceptibility to certain strains of T cell- trophic HIV. This appeared to be genetically determined because the susceptible or resistant phenotype was consistent for a given donor and a given HIV strain, and because it segregated in a family. Two years of work have demonstrated further that this differential susceptibility is genetically determined as judged by more family segregation studies, and that it appears to be a unique resistance which is a post-entry restriction of the virus and is not receptor-mediated. Other studies during this period have shown, also, that two cases of "transient" HIV infection in adults are associated with this host lymphocyte resistance. Two new cohorts of high-risk individuals have been established and are currently under study to determine the frequency of transient infection and if host genetic resistance to T cell-trophic HIV strains is playing a role in both transient infection and in resistance to infection. The specific aims of the project: (1) to map the viral determinant of this host resistance; (2) to map the resistance genes in the human genome; and (3) to demonstrate further whether these genes have a role in the human population in either preventing infection or retarding disease progression. In effect, the researchers in this project will characterize a third type of genetic resistance to HIV, adding to the HLA/TAP complex and the chemokine receptor polymorphisms.
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Determining Whether Transient HIV Infection Occurs
Determining Whether Transient HIV Infection Occurs
Determining Whether Transient HIV Infection Occurs
Studies of HIV Latency in Primary CD4 T-Lymphocytes
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