Exploiting Natural Killer cells in HIV/HBV co-infection to achieve eradication

Information

  • Research Project
  • 10082480
  • ApplicationId
    10082480
  • Core Project Number
    R01AI155182
  • Full Project Number
    1R01AI155182-01
  • Serial Number
    155182
  • FOA Number
    PAS-19-097
  • Sub Project Id
  • Project Start Date
    7/9/2020 - 4 years ago
  • Project End Date
    6/30/2025 - 6 months from now
  • Program Officer Name
    CHIOU, CHEN-CHIA CHRISTINE C
  • Budget Start Date
    7/9/2020 - 4 years ago
  • Budget End Date
    6/30/2021 - 3 years ago
  • Fiscal Year
    2020
  • Support Year
    01
  • Suffix
  • Award Notice Date
    7/9/2020 - 4 years ago
Organizations

Exploiting Natural Killer cells in HIV/HBV co-infection to achieve eradication

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.

IC Name
NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES
  • Activity
    R01
  • Administering IC
    AI
  • Application Type
    1
  • Direct Cost Amount
    440806
  • Indirect Cost Amount
    35264
  • Total Cost
    476070
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    855
  • Ed Inst. Type
  • Funding ICs
    NIAID:476070\
  • Funding Mechanism
    Non-SBIR/STTR RPGs
  • Study Section
    HIVD
  • Study Section Name
    HIV Immunopathogenesis and Vaccine Development Study Section
  • Organization Name
    UNIVERSITY OF OXFORD
  • Organization Department
  • Organization DUNS
    226694883
  • Organization City
    OXFORD
  • Organization State
  • Organization Country
    UNITED KINGDOM
  • Organization Zip Code
    OX1 2JD
  • Organization District
    UNITED KINGDOM