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Safety and virologic impact of the IL-15 superagonist N-803 in people living with HIV: a phase 1 trial.
Miller, Jeffrey S; Davis, Zachary B; Helgeson, Erika; Reilly, Cavan; Thorkelson, Ann; Anderson, Jodi; Lima, Noemia S; Jorstad, Siri; Hart, Geoffrey T; Lee, John H; Safrit, Jeffrey T; Wong, Hing; Cooley, Sarah; Gharu, Lavina; Chung, Hyunsoo; Soon-Shiong, Patrick; Dobrowolski, Curtis; Fletcher, Courtney V; Karn, Jonathan; Douek, Daniel C; Schacker, Timothy W.
Afiliação
  • Miller JS; Department of Medicine, University of Minnesota Medical School, Minneapolis, MN, USA.
  • Davis ZB; Department of Medicine, University of Minnesota Medical School, Minneapolis, MN, USA.
  • Helgeson E; Division of Biostatistics, University of Minnesota School of Public Health, Minneapolis, MN, USA.
  • Reilly C; Division of Biostatistics, University of Minnesota School of Public Health, Minneapolis, MN, USA.
  • Thorkelson A; Department of Medicine, University of Minnesota Medical School, Minneapolis, MN, USA.
  • Anderson J; Department of Medicine, University of Minnesota Medical School, Minneapolis, MN, USA.
  • Lima NS; Human Immunology Section, Vaccine Research Center, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA.
  • Jorstad S; Department of Medicine, University of Minnesota Medical School, Minneapolis, MN, USA.
  • Hart GT; Department of Medicine, University of Minnesota Medical School, Minneapolis, MN, USA.
  • Lee JH; ImmunityBio, Culver City, CA, USA.
  • Safrit JT; ImmunityBio, Culver City, CA, USA.
  • Wong H; HCW Biologics, Miramar, FL, USA.
  • Cooley S; HCW Biologics but was with Altor BioSciences at the start of the study, Miramar FL, USA.
  • Gharu L; Department of Medicine, University of Minnesota Medical School, Minneapolis, MN, USA.
  • Chung H; Fate Therapeutics, San Diego, CA, USA.
  • Soon-Shiong P; Human Immunology Section, Vaccine Research Center, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA.
  • Dobrowolski C; Human Immunology Section, Vaccine Research Center, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA.
  • Fletcher CV; ImmunityBio, Culver City, CA, USA.
  • Karn J; Department of Molecular Biology and Microbiology, Medical School, Case Western Reserve University, Cleveland, OH, USA.
  • Douek DC; Wallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology and Emory School of Medicine, Atlanta, GA, USA.
  • Schacker TW; Antiviral Pharmacology Laboratory, UNMC Center for Drug Discovery, University of Nebraska Medical Center, Omaha, NE, USA.
Nat Med ; 28(2): 392-400, 2022 02.
Article em En | MEDLINE | ID: mdl-35102335
ABSTRACT
There is no cure for HIV infection, and lifelong antiretroviral therapy (ART) is required. N-803 is an IL-15 superagonist comprised of an N72D mutant IL-15 molecule attached to its alpha receptor and a human IgG1 fragment designed to increase IL-15 activity. Preclinical studies with both HIV and SIV suggest that the drug has potential to reduce virus reservoirs by activating virus from latency and enhancing effector function. We conducted a phase 1 study of N-803 ( NCT02191098 ) in people living with HIV, the primary objective of which was to assess the safety and tolerability of the drug, with an exploratory objective of assessing the impact on peripheral virus reservoirs. ART-suppressed individuals were enrolled into a dose-escalation study of N-803 in four different cohorts (0.3, 1.0, 3.0 and 6.0 mcg kg-1). Each cohort received three doses total, separated by at least 1 week. We enrolled 16 individuals, of whom 11 completed all three doses. The maximum tolerated dose was 6.0 mcg kg-1. The primary clinical adverse events (AEs) reported were injection site rash and adenopathy, and four participants experienced a grade 1 or grade 2 QTc prolongation. No significant laboratory AEs attributable to N-803 were observed. In exploratory analyses, N-803 was associated with proliferation and/or activation of CD4+ and CD8+ T cells and natural killer cells that peaked at 4 d after dosing. IFN-γ, IP-10, MCP-1 and IL-15 increased during treatment. HIV transcription in memory CD4 T cells and intact proviral DNA initially increased after N-803 treatment; however, there was a small but significant decrease in the frequency of peripheral blood mononuclear cells with an inducible HIV provirus that persisted for up to 6 months after therapy. These data suggest that N-803 administration in ART-suppressed people living with HIV is safe and that larger clinical trials are needed to further investigate the effects of N-803 on HIV reservoirs.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Infecções por HIV / HIV-1 Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Infecções por HIV / HIV-1 Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article