MHC characterization in Chinese rhesus macaques
MHC characterization in Chinese rhesus macaques
批准号:
8541665
负责人:
Bianca Romina Mothe
金额:
$37.0万
依托单位国家:
美国
项目类别:
财政年份:
2005
资助国家:
美国
项目状态:
已结题
起止时间:
2005-05-15 至 2017-01-31
关键词:
Acquired Immunodeficiency SyndromeAllelesAnimalsBindingBiological AssayCaliforniaCellsChinese PeopleDataDideoxy Chain Termination DNA SequencingEpitopesExposure toGene FrequencyGoalsGrantHLA-A2 AntigenHLA-A3 AntigenHLA-B7 AntigenHumanImmune responseImmunogeneticsImmunologic MarkersIn VitroInfectionLaboratoriesLearningMacacaMacaca mulattaMajor Histocompatibility ComplexManuscriptsMethodsModelingPaperPeptidesPeripheral Blood Mononuclear CellPrimatesProcessPublicationsResearchResearch PersonnelSIVScientistStudentsTechnologyTestingTrainingUniversitiesVaccinesWashingtonWorkWritingbasecross reactivitydesignenzyme linked immunospot assayinterestnew technologynext generation sequencingnonhuman primatepublic health relevanceresearch study
中文摘要
描述(由申请人提供):我们将通过检测来自艾滋病感染的中国恒河猴的表达特定等位基因的细胞来确定HLA类比是否扩展到细胞反应性。我们还将确定在一组受感染动物中常见的MHC等位基因
英文摘要
DESCRIPTION (provided by applicant): We will determine if HLA analogy extends to cellular reactivity by testing cells from AIDS- infected Chinese rhesus macaques expressing specific alleles of interest. We will also identify MHC alleles that are common in a set of infected animals
and characterize them to identify SIV-specific epitopes. We propose to expand and continue the work we performed in our previous AREA grant. In the original grant, we characterized rhesus macaques based on the definition of MHC-peptide binding motifs, data from in vitro MHC-peptide binding assays, and have identified sets of analogous MHC molecules in humans and rhesus macaques. Analogous MHC molecules are defined as MHC molecules associated with a high degree of interspecies cross-reactivity (largely overlapping peptide binding repertoires). We now propose to advance these analyses using new technology consisting of next generation sequencing, to identify MHC molecules in a set of SIV-infected Chinese rhesus macaques. We will determine if HLA analogy extends to cellular reactivity by testing cells from SIV- infected Chinese rhesus macaques expressing specific alleles of interest. Furthermore, we will identify MHC alleles that are common in these infected animals and characterize them to identify SIV- specific epitopes. Our goal is also to understand HLA analogy from a functional perspective as well as identify any new commonly expressed MHC class I alleles. Accordingly, we propose the following specific aims: 1) To identify the complete set of MHC class I alleles in a set of SIVmac239- infected Chinese rhesus macaques using next generation sequencing. 2) To characterize MHC:peptide binding motifs and associated functional immune responses specific in Chinese rhesus macaques. Fifty-six Chinese rhesus macaques are being studied as part of a vaccine study at Washington National Primate Center. We already have preliminary MHC data on a subset of these animals as part of our previous AREA grant. These studies were performed using traditional Sanger sequencing methods. We will now expand the MHC typing of these efforts using next generation sequencing on the [MiSeq platform]. Upon MHC identification of these 56 animals, we will perform additional studies to characterize cellular immune responses. We will receive PBMC which we will use to analyze immune responses. From these data, we will be able to determine cellular reactivity in the context of analogous MHC alleles in Chinese rhesus macaque to HLA alleles and whether there are additional high frequency alleles.
期刊论文(3)
专著(0)
科研奖励(0)
会议论文
DOI:
10.1111/j.1600-0684.2011.00487.x
发表时间:
2011-08
期刊:
Journal of medical primatology
影响因子:
0.7
作者:
[Wambua D, Henderson R, Solomon C, Hunter M, Marx P, Sette A, Mothé BR]
通讯作者:
Mothé BR
DOI:
10.1007/s00251-010-0450-3
发表时间:
2010-07
期刊:
IMMUNOGENETICS
影响因子:
3.2
作者:
[Solomon, Christopher, Southwood, Scott, Hoof, Ilka, Rudersdorf, Richard, Peters, Bjoern, Sidney, John, Pinilla, Clemencia, Marcondes, Maria Cecilia Garibaldi, Ling, Binhua, Marx, Preston, Sette, Alessandro, Mothe, Bianca R.]
通讯作者:
Mothe, Bianca R.
DOI:
10.1007/s00251-010-0502-8
发表时间:
2011-05
期刊:
IMMUNOGENETICS
影响因子:
3.2
作者:
[Southwood, Scott, Solomon, Christopher, Hoof, Ilka, Rudersdorf, Richard, Sidney, John, Peters, Bjoern, Wahl, Angela, Hawkins, Oriana, Hildebrand, William, Mothe, Bianca R., Sette, Alessandro]
通讯作者:
Sette, Alessandro
The role of CD4+ Cell Responses in LCMV Infection
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批准号:7755821
-
项目类别:
-
资助金额:$11.1万
-
财政年份:2008
-
负责人:Bianca Romina Mothe
-
依托单位:
The role of CD4+ Cell Responses in LCMV Infection
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批准号:8015600
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项目类别:
-
资助金额:$10.99万
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财政年份:2008
-
负责人:Bianca Romina Mothe
-
依托单位:
The role of CD4+ Cell Responses in LCMV Infection
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批准号:7342586
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项目类别:
-
资助金额:$11.1万
-
财政年份:2008
-
负责人:Bianca Romina Mothe
-
依托单位:
The role of CD4+ Cell Responses in LCMV Infection
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批准号:7561094
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项目类别:
-
资助金额:$11.1万
-
财政年份:2008
-
负责人:Bianca Romina Mothe
-
依托单位:
MHC Analogy for Biodefense Animal Model Development
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批准号:6897721
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项目类别:
-
资助金额:$18.5万
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财政年份:2005
-
负责人:Bianca Romina Mothe
-
依托单位:
MHC analogy and T-cell activation in SIV infection
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批准号:7494893
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项目类别:
-
资助金额:$23.45万
-
财政年份:2005
-
负责人:Bianca Romina Mothe
-
依托单位:
海外基金