Time to Viral Rebound After Interruption of Modern Antiretroviral Therapies

Author:

Li Jonathan Z1,Aga Evgenia2,Bosch Ronald J2,Pilkinton Mark3,Kroon Eugène4,MacLaren Lynsay5,Keefer Michael6,Fox Lawrence7,Barr Liz8,Acosta Edward9,Ananworanich Jintanat410,Coombs Robert11,Mellors John W12,Landay Alan L13,Macatangay Bernard12,Deeks Steven14,Gandhi Rajesh T15,Smith Davey M16

Affiliation:

1. Brigham and Women’s Hospital, Harvard Medical School, Boston, Massachusetts, USA

2. Harvard T.H. Chan School of Public Health, Boston, Massachusetts, USA

3. Vanderbilt University, Nashville, Tennesee, USA

4. Thai Red Cross AIDS Research Centre, Bangkok, Thailand

5. Whitman Walker Clinic, Washington D.C., USA

6. University of Rochester School of Medicine and Dentistry, Rochester, New York, USA

7. National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA

8. ACTG Community Scientific Subcommittee, USA

9. University of Alabama at Birmingham, Birmingham, Alabama, USA

10. University of Amsterdam, Amsterdam, Netherlands

11. University of Washington, Seattle, Washington, USA

12. University of Pittsburgh, Pittsburgh, Pennsylvania, USA

13. Rush University Medical Center, Chicago, Illinois, USA

14. University of California, San Francisco, San Francisco, California, USA

15. Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA

16. Unversity of California, San Diego, San Diego, California, USA

Abstract

Abstract Background Development of human immunodeficiency virus (HIV) remission strategies requires precise information on time to HIV rebound after treatment interruption, but there is uncertainty regarding whether modern antiretroviral therapy (ART) regimens and timing of ART initiation may affect this outcome. Methods AIDS Clinical Trials Group (ACTG) A5345 enrolled individuals who initiated ART during chronic or early HIV infection and on suppressive ART for ≥2 years. Participants underwent carefully monitored antiretroviral interruption. ART was restarted upon 2 successive viral loads ≥1000 copies/mL. We compared participants of A5345 with participants of 6 historic ACTG treatment interruption studies. Results Thirty-three chronic-treated and 12 early-treated participants interrupted ART with evaluable time to viral rebound. Median time to viral rebound ≥1000 HIV RNA copies/mL was 22 days. Acute retroviral rebound syndrome was diagnosed in 9% of the chronic-treated and none of the early-treated individuals. All participants of the historic studies were on older protease inhibitor-based regimens, whereas 97% of A5345 participants were on integrase inhibitor-based ART. There were no differences in the timing of viral rebound comparing A5345 versus historic studies. In a combined analysis, a higher percentage of early-treated participants remained off ART at posttreatment interruption week 12 (chronic vs early: 2% vs 9%, P = .0496). One chronic-treated and one early-treated A5345 participant remained off ART for >24 weeks. All participants resuppressed after ART reinitiation. Conclusions Early ART initiation, using either older or newer ART regimens, was associated with a significant delay in the time to HIV rebound after ART interruption, lowering the barrier for HIV remission.

Funder

National Institute of Allergy and Infectious Diseases

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Microbiology (medical)

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