Exploiting Natural Killer cells in HIV/HBV co-infection to achieve eradication
Exploiting Natural Killer cells in HIV/HBV co-infection to achieve eradication
批准号:
10650148
负责人:
Dimitra Peppa
金额:
$33.56万
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:
未结题
起止时间:
2020-07-09 至 2025-06-30
关键词:
AntibodiesAutologousBloodCD8-Positive T-LymphocytesCell physiologyCellsChronicClinicalClinical TrialsDevelopmentEndosomesEndowmentExclusionExhibitsFine needle aspiration biopsyGenetic TranscriptionGoalsHIVHIV InfectionsHepaticHepatitis B InfectionHepatitis B VirusHumanImmuneImmune responseImmunologicsImmunotherapeutic agentKnowledgeLiverMalignant NeoplasmsMediatingMemoryMetabolicMolecularNatural Killer Cell ImmunotherapyNatural Killer CellsOutcomePathogenicityPathway interactionsPatientsPeripheralPhenotypePopulationProcessProductionPropertyProteomicsRecoveryReportingResidual stateResolutionRoleSiteT-Cell ActivationT-LymphocyteTestingTherapeuticTissuesToxic effectVaccinationVaccine TherapyViralVirusVirus DiseasesVirus ReplicationWorkantiretroviral therapyclinical materialco-infectioncohortcytokineeffective therapyefficacy evaluationenv Gene Productsexhaustionhigh riskimmune activationimmunoregulationinnovationneutralizing antibodynovelperipheral bloodreceptorresponserestraintsingle cell analysissingle-cell RNA sequencingtranscriptomics
中文摘要
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英文摘要
Exploiting adaptive NK cells in HIV/HBV co-infection towards eradication
Project Summary/Abstract
Despite the benefits of combined antiretroviral treatment (ART) with dual activity against HIV
and HBV, the differences in outcome between HIV/HBV co-infected and HBV mono-infected
populations still persist. Our current understanding of the degree of immunological recovery
with therapy in these two groups, in particular in terms of hepatic immune responses is scarce,
identifying a significant knowledge gap and a barrier to the development of effective functional
cures. Recent technical advances, including the use of single-cell RNA sequencing (scRNA-
seq) and high-throughput single cell analysis along with fine needle aspirates (FNAs) of the
liver from appropriately matched clinical cohorts provide new exciting opportunities to probe
hepatic versus peripheral immune signatures. These innovative approaches will be applied to
ascertain the transcriptional landscape, proteomic and functional features of immune cell
populations in the liver and peripheral blood between HIV/HBV co-infected versus HBV mono-
infected patients at an entirely new level of resolution. Particular emphasis will be placed on
Natural Killer (NK) cells with adaptive properties and unique subpopulations of NK cells with
‘memory’ features enriched in the liver. These specialised subpopulations that arise in
response to chronic viral infections and following vaccination with HIV-encoded envelope
protein and endowed with enhanced functionality hold tremendous potential for effective
control of virus replication. Therefore, clinical exploitation of adaptive NK cells represents a
transformative approach to augment therapy of chronic viral infection. We aim to develop a
robust and scalable platform for the expansion of adaptive NK cells with enhanced
functionality and predictable selectivity that could circumvent many of the limitations inherent
to the various immunotherapeutic approaches tested so far, representing a novel avenue for
new or complementary curative strategies.
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DOI:
10.3389/fimmu.2022.908697
发表时间:
2022
期刊:
Frontiers in immunology
影响因子:
7.3
作者:
[]
通讯作者:
DOI:
10.1038/s41577-021-00551-w
发表时间:
2021-05
期刊:
Nature reviews. Immunology
影响因子:
--
作者:
[Alrubayyi A, Peppa D]
通讯作者:
Peppa D
Attenuated humoral responses in HIV after SARS-CoV-2 vaccination linked to B cell defects and altered immune profiles.
SARS-COV-2疫苗接种后与B细胞缺陷和免疫谱改变的SARS-COV-2疫苗接种后,HIV中的体液反应减弱。
DOI:
10.1016/j.isci.2022.105862
发表时间:
2023-01-20
期刊:
ISCIENCE
影响因子:
5.8
作者:
[Touizer, Emma, Alrubayyi, Aljawharah, Ford, Rosemarie, Hussain, Noshin, Gerber, Pehuen Pereyra, Shum, Hiu-Long, Rees-Spear, Chloe, Muir, Luke, Gea-Mallorqui, Ester, Kopycinski, Jakub, Jankovic, Dylan, Jeffery-Smith, Anna, Pinder, Christopher L., Fox, Thomas A., Williams, Ian, Mullender, Claire, Maan, Irfaan, Waters, Laura, Johnson, Margaret, Madge, Sara, Youle, Michael, Barber, Tristan J., Burns, Fiona, Kinloch, Sabine, Rowland-Jones, Sarah, Gilson, Richard, Matheson, Nicholas J., Morris, Emma, Peppa, Dimitra, McCoy, Laura E.]
通讯作者:
McCoy, Laura E.
DOI:
10.1097/qad.0000000000003319
发表时间:
2022-11-15
期刊:
AIDS (London, England)
影响因子:
--
作者:
[]
通讯作者:
DOI:
10.1038/s41598-023-45412-9
发表时间:
2023-11-03
期刊:
SCIENTIFIC REPORTS
影响因子:
4.6
作者:
[Alrubayyi, Aljawharah, Touizer, Emma, Hameiri-Bowen, Dan, Charlton, Bethany, Gea-Mallorqui, Ester, Hussain, Noshin, da Costa, Kelly A. S., Ford, Rosemarie, Rees-Spear, Chloe, Fox, Thomas A., Williams, Ian, Waters, Laura, Barber, Tristan J., Burns, Fiona, Kinloch, Sabine, Morris, Emma, Rowland-Jones, Sarah, McCoy, Laura E., Peppa, Dimitra]
通讯作者:
Peppa, Dimitra
共 9 条
Exploiting Natural Killer cells in HIV/HBV co-infection to achieve eradication
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批准号:10447197
-
项目类别:
-
资助金额:$34.22万
-
财政年份:2020
-
负责人:Dimitra Peppa
-
依托单位:
Exploiting Natural Killer cells in HIV/HBV co-infection to achieve eradication
-
批准号:10399177
-
项目类别:
-
资助金额:$45.03万
-
财政年份:2020
-
负责人:Dimitra Peppa
-
依托单位:
Exploiting Natural Killer cells in HIV/HBV co-infection to achieve eradication
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批准号:10082480
-
项目类别:
-
资助金额:$47.61万
-
财政年份:2020
-
负责人:Dimitra Peppa
-
依托单位:
海外基金