Dissecting the signals that maintain HIV-specific CD8+ T cell exhaustion - administrative supplement
Dissecting the signals that maintain HIV-specific CD8+ T cell exhaustion - administrative supplement
批准号:
10158069
负责人:
Rachel Lena Rutishauser
金额:
$5.4万
依托单位国家:
美国
项目类别:
财政年份:
2020
资助国家:
美国
项目状态:
已结题
起止时间:
2020-08-17 至 2023-01-31
关键词:
Administrative SupplementAntigensAreaBlood CellsBlood specimenCD8-Positive T-LymphocytesCell physiologyCellsCellular biologyChronicClinicalClinical ResearchCommunicable DiseasesDevelopmentDiseaseDisease remissionDoctor of PhilosophyEffector CellFundingGenetic TranscriptionGoalsHIVHIV InfectionsHumanImmune responseImmunologicsImmunologistImmunologyIndividualInfection ControlInflammationInterleukin-1 betaInterventionLaboratoriesMHC Class I GenesMalignant NeoplasmsMemoryMentored Patient-Oriented Research Career Development AwardMentorsPathogenesisPhenotypeProliferatingResearchResearch PersonnelResearch PrioritySchoolsScientistSignal TransductionSpecialistT cell differentiationTissuesToxic effectTrainingUnited States National Institutes of HealthVaccine TherapyVaccinesantiretroviral therapybasecareerchronic infectioncohorteffective therapyexhaustexhaustionimmune activationimmunomodulatory therapiesinhibitor/antagonistlymph nodesnovel therapeuticsnovel vaccinesparent grantpatient oriented researchperipheral bloodprogramsrecruitregenerativeskillstherapeutic developmenttranscriptomicstranslational scientist
中文摘要
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英文摘要
PROJECT SUMMARY OF PARENT GRANT
This is an application for a K23 award for Dr. Rachel Rutishauser, MD, PhD, is establishing herself as a
young investigator in patient-oriented studies of HIV immunology. Her goal is to apply her PhD graduate
school background in basic CD8+ T cell biology to study the mechanisms that underlie protective and
dysfunctional immune responses in HIV infection. Nearly forty million people worldwide are infected with
HIV and identifying interventions to induce HIV remission or cure is an NIH high priority research area.
Many approaches propose to do so by eliciting protective HIV-specific CD8+ T cells. However, in order to be
effective, these therapies need to overcome HIV-specific CD8+ T cell exhaustion. Exhaustion is defined as
a loss in the regenerative capacity of antigen-specific CD8+ T cells to proliferate and generate functional
effector cells. This K23 award will provide Dr. Rutishauser with the support to explore how HIV-specific CD8
+ T cell exhaustion is regulated by: (1) memory CD8+ T cell-associated transcriptional programs, (2) tissue
microenvironments, and (3) chronic inflammation. Specifically, she will perform phenotypic, functional, and
single-cell transcriptomic analysis of HIV-specific MHC Class I tetramer+ CD8+ T cells from the peripheral
blood, lymph node, and gut tissue of thirty HIV-infected individuals who she will recruit from the UCSF-
based SCOPE cohort from three clinical groups: individuals who naturally control infection (controllers), as
well as non-controllers on and off of antiretroviral therapy (ART). She will also determine if reducing chronic
inflammation can enhance HIV-specific CD8+ T cell function by leveraging peripheral blood samples from
an ongoing NIH-funded clinical study (NCT02272946) of ART-suppressed HIV-infected individuals who are
administered the IL-1β inhibitor, canakinumab. To achieve these goals, Dr. Rutishauser will be co-mentored
by Dr. Peter Hunt, an HIV translational immunologist and expert in the mechanisms of HIV immune
activation, Dr. Joseph Mike McCune, a laboratory-based scientist who has made several fundamental
discoveries about HIV pathogenesis, Dr. Steven Deeks, a leader in the HIV cure field, and Dr. Mark Ansel,
an immunologist with expertise in T cell differentiation. Through a focused program of mentored training and
coursework, the candidate will develop advanced skills in clinical research, human translational
immunology, and single-cell transcriptional analysis. The results of these studies are anticipated to be
directly relevant to HIV cure research and widely applicable to developing treatments for other disease
states in which exhausted antigen-specific CD8+ T cells arise, such as other chronic infections and cancer.
Ultimately, the training and research plans outlined here will support Dr. Rutishauser as she transitions from
being a basic immunologist and clinical infectious disease specialist to being a translational researcher
equipped with the skills to pursue an independent career focused on elucidating the fundamental principles
of CD8+ T cell biology and informing the development of therapeutics and vaccines for infectious diseases.
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Targeting HIV-specific T cell differentiation programs to enhance post-treatment control of HIV
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批准号:10483785
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项目类别:
-
资助金额:$79.15万
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财政年份:2022
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负责人:Rachel Lena Rutishauser
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依托单位:
Targeting HIV-specific T cell differentiation programs to enhance post-treatment control of HIV
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批准号:10552650
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项目类别:
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资助金额:$81.4万
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财政年份:2022
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负责人:Rachel Lena Rutishauser
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依托单位:
Dissecting the signals that maintain HIV-specific CD8+ T cell exhaustion
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批准号:10330433
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项目类别:
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资助金额:$20.84万
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财政年份:2018
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负责人:Rachel Lena Rutishauser
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项目类别:省市级项目
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批准年份:2008
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依托单位: