Mission Remission: Integrated characterization of the HIV Reservoir and Host Immune Responses after Antibody-Immunotherapy
This project aims to investigate the mechanisms behind higher rates of HIV remission through antibody-based immunotherapy to develop effective, drug-free HIV cure strategies.
Projectdetails
Introduction
The search for a therapeutic intervention that can lead to HIV remission or cure is a global priority of the HIV field. HIV-specific antibodies have the potential to alter the clinical course of infection and enhance antiviral immune responses.
Recent Findings
In addition, we have recently demonstrated that antibody-based HIV immunotherapy results in higher-than-average cases of durable HIV remission in the absence of antiretroviral medication.
Impact on HIV Reservoir
Moreover, passive administration of HIV-specific antibodies was associated with reductions in the size of the replication-competent HIV reservoir, which is the major barrier towards a cure for HIV.
Importance of Understanding Mechanisms
While these results highlight the exceptional potential of HIV immunotherapy, it is critical to understand the underlying mechanisms responsible for higher rates of HIV remission and antibody-mediated changes in the reservoir.
Research Objectives
Therefore, we will identify individuals with long-term HIV remission from clinical antibody-immunotherapy trials before comprehensively characterizing:
- Host immune responses
- Host-viral gene expression
- The HIV latent reservoir
By combining highly valuable clinical samples with novel strategies for the characterization of viral immunity and persistence, we aim to establish a relationship between:
- Antibody-based HIV immunotherapy
- Host immunological factors
- Adaptive immune responses
- The nature of the viral reservoir
With the overarching goal of developing clinical interventions for long-term, drug-free HIV remission or cure.
Financiële details & Tijdlijn
Financiële details
Subsidiebedrag | € 1.498.130 |
Totale projectbegroting | € 1.498.130 |
Tijdlijn
Startdatum | 1-11-2024 |
Einddatum | 31-10-2029 |
Subsidiejaar | 2024 |
Partners & Locaties
Projectpartners
- CHARITE - UNIVERSITAETSMEDIZIN BERLINpenvoerder
Land(en)
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The project aims to understand and reverse vaccine hypo-responsiveness across populations by investigating immunological and metabolic factors, ultimately improving vaccine efficacy globally.
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This project aims to use CRISPR/Cas9 technology with HIV-1 to uncover antiviral mechanisms, enhancing our understanding and control of viral pathogens for better prevention and therapy.
REVisiting Antibody structures and repertoires through advances in Mass spectrometry and Proteomics
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Tracing virus-specific CD8+ T cell clonotype zonation and function in humans
This project aims to redefine the role and distribution of CD8+ T cells in viral immunity using single-cell technologies, focusing on their function against SARS-CoV-2 and informing future vaccine development.
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InnomABs
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