4.4 Article

Preserved central nervous system functioning after use of romidepsin as a latency-reversing agent in an HIV cure strategy

Journal

AIDS
Volume 36, Issue 3, Pages 363-372

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/QAD.0000000000003121

Keywords

central nervous system; histone deacetylase inhibitors; HIV infection; kick&kill strategies; MVA; HIVconsv; romidepsin

Funding

  1. ISCIII [PI15/01188]
  2. HIVACAT Catalan research program
  3. Fundacio Gloria Soler
  4. Medical Research Council (MRC) UK
  5. UK Department for International Development (DFID) under the MRC/DFID Concordat agreements [G0701669]
  6. Fundacio Lluita Contra la SIDA [L1604]
  7. P-FIS grant [FI17/00294]
  8. Institut d'Investigacions Biomediques August Pi i Sunyer (IDIBAPS), Barcelona, Spain
  9. European Union's Horizon 2020 research and innovation programme [681137, SAF201789726-R]
  10. NEIDA [PO1-AI131568a]

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This study aimed to assess the impact of a kick&kill HIV cure strategy on the central nervous system (CNS) using a therapeutic vaccine and a latency-reversing agent. The results showed no detrimental effects on cognitive status, functional outcomes, or brain imaging parameters in early-treated HIV-infected individuals. The safety of CNS was also confirmed after the treatment.
Objective: To assess the central nervous system (CNS) impact of a kick&kill HIV cure strategy using therapeutic vaccine MVA.HIVconsv and the histone deacetylase inhibitor (HDACi) romidepsin (RMD) as latency-reversing agent. Design: Neurological observational substudy of the BCN02 trial (NCT02616874), a proof-of-concept, open-label, single-arm, phase I clinical trial testing the safety and immunogenicity of the MVA.HIVconsv vaccine and RMD in early-treated HIV-1-infected individuals. A monitored antiretroviral pause (MAP) was performed, with cART resumption after 2 pVL more than 2000 copies/ml. Reinitiated participants were followed for 24 weeks. Methods: Substudy participation was offered to all BCN02 participants (N = 15). Evaluations covered cognitive, functional, and brain imaging outcomes, performed before RMD administration (pre-RMD), after three RMD infusions (post-RMD), and at the end of the study (EoS). A group of early-treated HIV-1-infected individuals with matched clinical characteristics was additionally recruited (n = 10). Primary endpoint was change in a global cognitive score (NPZ-6). Results: Eleven participants from BCN02 trial were enrolled. No significant changes were observed in cognitive, functional, or brain imaging outcomes from pre-RMD to post-RMD. No relevant alterations were detected from pre-RMD to EoS either. Scores at EoS were similar in participants off cART for 32 weeks (n = 3) and those who resumed therapy for 24 weeks (n = 7). Controls showed comparable punctuations in NPZ-6 across all timepoints. Conclusion: No detrimental effects on cognitive status, functional outcomes, or brain imaging parameters were observed after using the HDACi RMD as latency-reversing agent with the MVA.HIVconsv vaccine in early-treated HIV-1-infected individuals. CNS safety was also confirmed after completion of the MAP.

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