R37AI189285
Project Grant
Overview
Grant Description
Characterization of allogeneic T cells mediating HIV cure - Project summary
With the most people ever in history currently living with HIV, stopping the HIV epidemic remains imperative.
Combination antiretroviral therapy (ART) limits viral replication, but is not curative.
Thus, there is an urgent need to design a functional cure via elimination of the viral reservoir.
Five individuals, Timothy Brown (Berlin patient), Adam Castillejo (London patient), Paul Edmonds (City of Hope patient), Marc Franke (Düsseldorf patient), and the New York City patient who has not released their identity were cured of HIV following leukemia-related, MHC-matched, allogeneic hematopoietic stem cell transplantation (ALLOSCT).
How ALLOSCT mediates cure of HIV is unknown.
Using our ALLOSCT model in Mauritian cynomolgus macaque (MCM), we have demonstrated that the allogeneic immune response can potently purge the latent reservoir.
Therefore, we hypothesize that allogeneic T cell responses targeting minor antigens mediate HIV cure similar to how they mediate cure of leukemia.
We propose here to define the allogeneic T cell responses in both the individuals who were cured of HIV, as well as the two MCM cured of SIV following ALLOSCT.
In Specific Aim 1, we will define the allogeneic T cell responses and their targets in three of the individuals cured of HIV (Adam, Paul, and Marc), as well in a number of other cases where individuals underwent ALLOSCT and experienced a disappearance of HIV from the blood.
In Specific Aim 2, we will define the allogeneic T cell responses and their targets in the two MCM cured of SIV post ALLOSCT, as well as in a further longitudinal cohort of SIV+ MCM that underwent ALLOSCT and experienced a decrease in the viral reservoir.
In Aim 3, we will adoptively transfer T cells expressing human or MCM allogeneic T cell receptors into HIV+ humanized mice or SIV+ MCM, respectively, to measure the safety and efficacy of allogeneic T cells for HIV cure.
This work would expand our knowledge of the mechanism of HIV cure in the setting of allogeneic HSCT and establish a new therapeutic approach for HIV cure.
With the most people ever in history currently living with HIV, stopping the HIV epidemic remains imperative.
Combination antiretroviral therapy (ART) limits viral replication, but is not curative.
Thus, there is an urgent need to design a functional cure via elimination of the viral reservoir.
Five individuals, Timothy Brown (Berlin patient), Adam Castillejo (London patient), Paul Edmonds (City of Hope patient), Marc Franke (Düsseldorf patient), and the New York City patient who has not released their identity were cured of HIV following leukemia-related, MHC-matched, allogeneic hematopoietic stem cell transplantation (ALLOSCT).
How ALLOSCT mediates cure of HIV is unknown.
Using our ALLOSCT model in Mauritian cynomolgus macaque (MCM), we have demonstrated that the allogeneic immune response can potently purge the latent reservoir.
Therefore, we hypothesize that allogeneic T cell responses targeting minor antigens mediate HIV cure similar to how they mediate cure of leukemia.
We propose here to define the allogeneic T cell responses in both the individuals who were cured of HIV, as well as the two MCM cured of SIV following ALLOSCT.
In Specific Aim 1, we will define the allogeneic T cell responses and their targets in three of the individuals cured of HIV (Adam, Paul, and Marc), as well in a number of other cases where individuals underwent ALLOSCT and experienced a disappearance of HIV from the blood.
In Specific Aim 2, we will define the allogeneic T cell responses and their targets in the two MCM cured of SIV post ALLOSCT, as well as in a further longitudinal cohort of SIV+ MCM that underwent ALLOSCT and experienced a decrease in the viral reservoir.
In Aim 3, we will adoptively transfer T cells expressing human or MCM allogeneic T cell receptors into HIV+ humanized mice or SIV+ MCM, respectively, to measure the safety and efficacy of allogeneic T cells for HIV cure.
This work would expand our knowledge of the mechanism of HIV cure in the setting of allogeneic HSCT and establish a new therapeutic approach for HIV cure.
Funding Goals
NOT APPLICABLE
Grant Program (CFDA)
Awarding / Funding Agency
Place of Performance
Portland,
Oregon
972393011
United States
Geographic Scope
Single Zip Code
Related Opportunity
Analysis Notes
Amendment Since initial award the total obligations have increased 99% from $1,657,972 to $3,297,069.
Oregon Health & Science University was awarded
Allogeneic T Cell Responses HIV Cure: Mechanism Therapeutic Potential
Project Grant R37AI189285
worth $3,297,069
from the National Institute of Allergy and Infectious Diseases in June 2025 with work to be completed primarily in Portland Oregon United States.
The grant
has a duration of 5 years and
was awarded through assistance program 93.855 Allergy and Infectious Diseases Research.
The Project Grant was awarded through grant opportunity NIH Research Project Grant (Parent R01 Clinical Trial Not Allowed).
Status
(Ongoing)
Last Modified 6/22/26
Period of Performance
6/16/25
Start Date
5/31/30
End Date
Funding Split
$3.3M
Federal Obligation
$0.0
Non-Federal Obligation
$3.3M
Total Obligated
Activity Timeline
Subgrant Awards
Disclosed subgrants for R37AI189285
Transaction History
Modifications to R37AI189285
Additional Detail
Award ID FAIN
R37AI189285
SAI Number
R37AI189285-171285046
Award ID URI
SAI UNAVAILABLE
Awardee Classifications
Public/State Controlled Institution Of Higher Education
Awarding Office
75NM00 NIH National Institute of Allergy and Infectious Diseases
Funding Office
75NM00 NIH National Institute of Allergy and Infectious Diseases
Awardee UEI
NPSNT86JKN51
Awardee CAGE
0YUJ3
Performance District
OR-01
Senators
Jeff Merkley
Ron Wyden
Ron Wyden
Modified: 6/22/26