Stable Latent HIV Infection and Low-level Viremia Despite Treatment With the Broadly Neutralizing Antibody VRC07-523LS and the Latency Reversal Agent Vorinostat
Author(s) -
Cynthia L. Gay,
Katherine S. James,
Marina Tuyishime,
Shane D. Falcinelli,
Sarah Joseph,
Matthew Moeser,
Brigitte Allard,
Jennifer Kirchherr,
Matthew L. Clohosey,
Samuel L M Raines,
David C. Montefiori,
Xiaoying Shen,
Robert J. Gorelick,
Lúcio Gama,
Adrian B. McDermott,
Richard A. Koup,
John R. Mascola,
Michelle Floris-Moore,
JoAnn Kuruc,
Guido Ferrari,
Joseph J. Eron,
Nancie M. Archin,
David M. Margolis
Publication year - 2021
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1093/infdis/jiab487
Subject(s) - viremia , virology , antibody , vorinostat , neutralizing antibody , immunology , viral load , biology , medicine , human immunodeficiency virus (hiv) , dna , genetics , histone deacetylase , histone
We tested the combination of a broadly neutralizing HIV antibody with the latency reversal agent vorinostat (VOR). Eight participants received 2 month-long cycles of VRC07-523LS with VOR. Low-level viremia, resting CD4+ T-cell–associated HIV RNA (rca-RNA) was measured, and intact proviral DNA assay (IPDA) and quantitative viral outgrowth assay (QVOA) were performed at baseline and posttreatment. In 3 participants, IPDA and QVOA declines were accompanied by significant declines of rca-RNA. However, no IPDA or QVOA declines clearly exceeded assay variance or natural decay. Increased resistance to VRC07-523LS was not observed. This combination therapy did not reduce viremia or the HIV reservoir. Clinical Trials Registration. NCT03803605.
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