State of the ART: HIV Cure – where are we now and where are we going?
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Transcript of State of the ART: HIV Cure – where are we now and where are we going?
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The views expressed are those of the authors and should not be construed to represent the positions of the U.S. Army or the Department of Defense.
State of the ART: HIV Cure – where are we now and where are we going?
Jintanat Ananworanich, MD, PhD
Associate Director for Therapeutics ResearchUS Military HIV Research Program (MHRP)
Maryland, USA
Deputy Director of SEARCH The Thai Red Cross AIDS Research Center
Bangkok, Thailand
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Outline
Is HIV cure possible? HIV persistence
Cure Strategies
Ethical and social considerations
Short video on patients’ perspectives on cure
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A Case of Cure
The Berlin PatientOff ART 6 years
Treatment CCR5-/- bone marrow transplant
Mechanism Make cells Resistant to HIV
Lesson Eliminate CCR5+/+ cells
Hutter G, NEJM 2009; Allers K, Blood 2011; Yukl SA, Plos Pathogens 2013;
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Transient but Encouraging HIV Remission
Two Boston Patients1,2
The Mississippi Child3
Treatment CCR5+/+bone marrow
transplant
Early ART
Off ART 3 months and 7 months
2.5 years
Lesson Delayed viral rebound is achievableBut unknown biomarkers for HIV remission
1Henrich T, JID 2013; 2Annals Internal Medicine (in press); 3Persaud D, NEJM 2014
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HIV Persistence
cell death
resting state
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Measuring the HIV Reservoir
Total HIV DNA
Replication competent
virus
Ho, Cell, 2013; Cillo, PNAS 2014
Integrated HIV DNA
HIV DNA (100%)
Replication competent (0.1%)
Intact, inducible (10%)
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Reservoir and Immunity
Boston patients
Mississippi child
immunity
latentvirus
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Strategies to Eliminate HIV Persistence
Before HIV Infection
Viral LoadSuppressed
“Shock and Kill”Eliminate Infected CellsVaccine
Chronic HIV Infection
Possible interventions:
• Latency reversing agents
• Broadly neutralizing antibody
• Gene-editing therapy
AcuteHIV Infection
ART
HIV RNA
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Novel vaccine given before exposuremay aid in viral control: SIV/macaque
model
Hansen SG and Picker LJ, Nature 2013
No protection
but
Virus eradicated in
50%
Controllers (n=9)
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VISCONTI Cohort of Post-Treatment Controllers
Why are these patients able to control HIV without ART?
HIV reservoir amount and location?
✔ Low HIV DNA✔ In shorter-lived CD4 cells
Saez-Cirion A, Plos Pathogens 2013
14 peopleART in first3 months
Control VLafter
stopping ART
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Early ART limits persistence of HIV reservoir in Long-lived CD4+ T cell subsets (RV254/SEARCH010)
Nicolas Chomont (VGTI-Florida)Updated from Ananworanich J, 2013 CROI
Long-lived central memory
CD4+ T cells
100%
63%
0%
Duration of HIVat ART initiation
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Early ART in Infants
Three US teenagers treated from infancy have no replication competent HIV Luzuriaga K, JID 2014
N=15 Ananworanich J, AIDS 2014
Viscontipost treatment
controllers
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Shocked but not KilledHDACi Panobinostat
days
Fol
d in
crea
se in
CA
-US
RN
A
ANOVA p<0.0001
Replication competent virus did not decline
Rasmussen et al, 2014 CROI
n=16
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Broadly Neutralizing Antibody
• > 30 antibodies identified
• Human studies
• VRC01: RV397/398 in acute HIV
• 3BNC117, 10-1074, PGT121
Viral clearanceCell death
Barouch DH, Nature 2013
0 20 40 60 80 1002
3
4
5
6Viral load suppression
in macaques(n=3)
VL
log
Days after infusion
PGT121
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Gene therapy to eliminate CCR5
LeukapharesisCD4+ T-cell isolation
ZFN cutCCR5 gene
Re-infuse
Tebas P, NEJM 2014
CCR5-
CCR5+
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Examples of strategies currently in human studies
SHOCKReactivating latently-
infected cellsInhibit histone deacetylase
Inhibit bromodomain extraterminal
Activate toll-like receptors Activate protein kinase C
KILLViral clearance by the
immune systemBroadly neutralizing antibodies
Therapeutic HIV vaccines Anti programmed cell
death (PD)1Anti PD ligand 1
HIV RESISTANT CELLSTransfusing cells without CCR5 gene
Gene-editing therapyBone marrow or cord blood transplantation
MINIMIZE RESERVOIRLimit reservoir with early treatment
Antiretroviral therapyBroadly neutralizing antibodies
Combination Cure
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HIV Cure and Cure Research:Social and Ethical
Considerations
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Societal and Individual Expectation
Eradicated = normal or free of disease or healed
Long-term adverse consequences of HIV New normal
Long-term monitoring of viral load
Stigma and discrimination
When to call someone “cured”?1
Best measure of reservoir is not known HIV remission
• VSLLDOTtime = Viral Suppression Off ART
1Forum Cure Project (V. Miller)
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Australian Participants’ Priorities on Outcomes of Cure Research
20 participants with chronic HIV infection in vorinostat (HDACi) trial
McMahon J, Elliott J and Lewin S, 2013 IAS
No longer needing to see a doctor
Stopping HIV medications
Being considered as a person not infected with HIV
Not getting HIV a second time
Not passing virus onto others
0 5 10 15 20 25 30 35 40 45 50
0
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Ethics of HIV cure
Ideal candidates are persons who are well with viral suppression
Potentially toxic interventions
ART interruption
Cost and accessibility
Shah SK, Lancet ID 2014; Lo B and Grady C, Curr Opin HIV AIDS 2013
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Preventive HIV Vaccine
-Prevent infection -Modulate immunity to limit viral reservoir
Early DiagnosisEarly Treatment
-Limit HIV reservoir and replication
Novel Therapy-Eliminate all cells capable of producing HIV
What might the future look like?
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Acknowledgements
Monash UniversitySharon Lewin
Thai Red Cross AIDS Research CenterPraphan PhanuphakNittaya PhanuphakSuteeraporn Pinyakorn
Johns Hopkins UniversityRobert SilicianoDeborah PersaudAlison HIll
Vaccine and Gene Therapy Institute-FloridaNicolas Chomont
Aarhus UniversityLars Ostergaard
US Military HIV Research ProgramNelson MichaelJerome KimMerlin RobbLisa Reilly
Study Volunteers and Research TeamsRV254/SEARCH010 acute HIV and HIV-NAT 194/pediatric reservoir
Purple HazeTarandeep AnandChattiya Nitpolprasert
UCSFSteve Deeks
Oregon Health Science UniversityLouis Picker
NIAID, NIHAnthony Fauci
Northwestern UniversityEllen Chadwick
University of PennsylvaniaPablo Tebas
University of PittsburgJohn Mellors
Harvard UniversityDan Barouch
Funding for Acute Infection Study RV254 provided by U.S NIH, U.S. DoD and amfAR
Institut PasteurAsier Saez-Cirion
NICHD, NIHLynne Mofenson
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“What does HIV cure mean to me?”
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