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Improved Nanoparticle Targeting of Tissue Myeloid Cells for HIV-1 Long-acting Pre-exposure Prophylaxis

Award Number: R01AI175068
ORGANIZATION: NATIONAL INSTITUTE OF ALLERGY & INFECTIOUS DISEASES
OPDIV: NIH
AWARD CLASS: DISCRETIONARY
AWARD ACTIVITY TYPE: SCIENTIFIC/HEALTH RESEARCH (INCLUDES SURVEYS)
PERIOD OF PERFORMANCE START DATE: 03/17/2023
PERIOD OF PERFORMANCE END DATE: 02/28/2027

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Improved Nanoparticle Targeting of Tissue Myeloid Cells for HIV-1 Long-acting Pre-exposure Prophylaxis - Summary Antiretroviral pre-exposure prophylaxis (PrEP) is an important tool for preventing transmission to virus naïve individuals and plays an important role in current efforts to end the HIV epidemic. If taken daily current oral PrEP strategies reliably block HIV transmission. However, the requirement of strict adherence to daily pill uptake, pill fatigue and other institutional barriers to access leave oral PrEP underutilized. Long-acting injectable PrEP strategies have the potential to address many of the problems associated with oral PrEP but the realization of drug formulations and delivery strategies that ensure sustained drug release for at least three months has remained challenging and motivates the development of entirely new long-acting PrEP strategies. This project develops a long-acting injectable PrEP strategy based on membrane-wrapped nanoparticles (NPs) that establish cellular depots for sustained maintenance of inhibitory concentrations of antiretrovirals (ARVs) at primary tissue sites of HIV-1 transmission in the female genital tract (FGT) and rectum. Selective targeting of CD169-expressing macrophages and dendritic cells is accomplished through incorporation of the ganglioside GM3 in the NP membrane. GM3-CD169 binding triggers uptake and sequestration of NPs in non-endolysosomal compartments that share distinct similarities with virus containing compartments (VCCs) in tissue-associated macrophages and dendritic cells. These compartments represent protected sites from where NPs can release drugs into the surrounding tissue for an extended period of time. Membrane-wrapped inverse micelles of block copolymers will be engineered as a GM3-NP platform for long-acting PrEP. A combination of long-acting tenofovir (TFV) and emtricitabine (FTC) prodrugs will be used as active compounds to validate the approach. The block copolymer NPs will contain TFV covalently linked to a polymer shell that encapsulates an aqueous core holding FTC conjugated to dendrimers. After quantifying drug loading and release in vitro, the GM3-mediated targeting of CD169+ myeloid cells in the FGT and rectum of a humanized mouse model will be tested. In parallel, the GM3- NP platform will be optimized to achieve sustained drug release in the target tissues. The hypothesis that the optimized NPs provide protection from mucosal HIV infection in a humanized mouse model for at least three months will be tested. The specific aims of this application are: Aim 1: To develop membrane-wrapped multicomponent NPs for sustained release of TFV/FTC. Aim 2: To target CD169-expressing myeloid cells in the FGT and SLTs for sustained TFV/FTC release. Aim 3: To demonstrate long-term protection from mucosal HIV-1 transmission in humanized mice by TFV/FTC incorporating GM3-NPs.


Issue Date FY	Funding FY	Legal Entity Name	Legal Entity Address	Legal Entity City	Legal Entity State	Legal Entity Zip Code	Legal Entity COUNTY	Legal Entity COUNTRY	Assistance Listing	Award Code	Budget Year	Action Date	Action Type	Action Amount

Issue Date FY: 2026 ( Subtotal = $703,756 )
2026	2026	TRUSTEES OF BOSTON UNIVERSITY	1 SILBER WAY	BOSTON	MA	02215	SUFFOLK	USA	Allergy and Infectious Diseases Research	000	4	2/19/2026	NON-COMPETING CONTINUATION	$703,756
														Subtotal = $703,756

Issue Date FY: 2025 ( Subtotal = $657,525 )
2025	2025	TRUSTEES OF BOSTON UNIVERSITY	1 SILBER WAY	BOSTON	MA	02215	SUFFOLK	USA	Allergy and Infectious Diseases Research	000	3	3/28/2025	NON-COMPETING CONTINUATION	$657,525
														Subtotal = $657,525

Issue Date FY: 2024 ( Subtotal = $788,992 )
2024	2024	TRUSTEES OF BOSTON UNIVERSITY	1 SILBER WAY	BOSTON	MA	02215	SUFFOLK	USA	Allergy and Infectious Diseases Research	000	2	2/20/2024	NON-COMPETING CONTINUATION	$710,093
2024	2024	TRUSTEES OF BOSTON UNIVERSITY	1 SILBER WAY	BOSTON	MA	02215	SUFFOLK	USA	Allergy and Infectious Diseases Research	002	2	7/2/2024	NON-COMPETING CONTINUATION	$0
2024	2024	TRUSTEES OF BOSTON UNIVERSITY	1 SILBER WAY	BOSTON	MA	02215	SUFFOLK	USA	Allergy and Infectious Diseases Research	001	2	5/23/2024	NON-COMPETING CONTINUATION	$78,899
														Subtotal = $788,992

Issue Date FY: 2023 ( Subtotal = $787,467 )
2023	2023	TRUSTEES OF BOSTON UNIVERSITY	1 SILBER WAY	BOSTON	MA	02215	SUFFOLK	USA	Allergy and Infectious Diseases Research	000	1	3/17/2023	NEW	$787,467
2023	2023	TRUSTEES OF BOSTON UNIVERSITY	1 SILBER WAY	BOSTON	MA	02215	SUFFOLK	USA	Allergy and Infectious Diseases Research	002	1	6/14/2023	NEW	$0
2023	2023	TRUSTEES OF BOSTON UNIVERSITY	1 SILBER WAY	BOSTON	MA	02215	SUFFOLK	USA	Allergy and Infectious Diseases Research	001	1	5/18/2023	NEW	$0
														Subtotal = $787,467

Grand Total All Awards = $2,937,740

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Improved Nanoparticle Targeting of Tissue Myeloid Cells for HIV-1 Long-acting Pre-exposure Prophylaxis

Award Number: R01AI175068

ORGANIZATION: NATIONAL INSTITUTE OF ALLERGY & INFECTIOUS DISEASES

OPDIV: NIH

AWARD CLASS: DISCRETIONARY

AWARD ACTIVITY TYPE: SCIENTIFIC/HEALTH RESEARCH (INCLUDES SURVEYS)

PERIOD OF PERFORMANCE START DATE: 03/17/2023

PERIOD OF PERFORMANCE END DATE: 02/28/2027

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