The human IL-15 superagonist N-803 promotes migration of virus-specific CD8+ T and NK cells to B cell follicles but does not reverse latency in ART-suppressed, SHIV-infected macaques.
Animals
Anti-Retroviral Agents
/ administration & dosage
B-Lymphocytes
/ cytology
CD8-Positive T-Lymphocytes
/ cytology
Cell Movement
/ drug effects
Disease Models, Animal
HIV Infections
/ drug therapy
HIV-1
/ drug effects
Humans
Interleukin-15
/ antagonists & inhibitors
Killer Cells, Natural
/ cytology
Lymph Nodes
/ drug effects
Macaca mulatta
Proteins
/ administration & dosage
Recombinant Fusion Proteins
Simian Acquired Immunodeficiency Syndrome
/ drug therapy
Simian Immunodeficiency Virus
/ drug effects
Virus Latency
/ drug effects
Journal
PLoS pathogens
ISSN: 1553-7374
Titre abrégé: PLoS Pathog
Pays: United States
ID NLM: 101238921
Informations de publication
Date de publication:
03 2020
03 2020
Historique:
received:
04
10
2019
accepted:
20
01
2020
revised:
24
03
2020
pubmed:
13
3
2020
medline:
7
7
2020
entrez:
13
3
2020
Statut:
epublish
Résumé
Despite the success of antiretroviral therapy (ART) to halt viral replication and slow disease progression, this treatment is not curative and there remains an urgent need to develop approaches to clear the latent HIV reservoir. The human IL-15 superagonist N-803 (formerly ALT-803) is a promising anti-cancer biologic with potent immunostimulatory properties that has been extended into the field of HIV as a potential "shock and kill" therapeutic for HIV cure. However, the ability of N-803 to reactivate latent virus and modulate anti-viral immunity in vivo under the cover of ART remains undefined. Here, we show that in ART-suppressed, simian-human immunodeficiency virus (SHIV)SF162P3-infected rhesus macaques, subcutaneous administration of N-803 activates and mobilizes both NK cells and SHIV-specific CD8+ T cells from the peripheral blood to lymph node B cell follicles, a sanctuary site for latent virus that normally excludes such effector cells. We observed minimal activation of memory CD4+ T cells and no increase in viral RNA content in lymph node resident CD4+ T cells post N-803 administration. Accordingly, we found no difference in the number or magnitude of plasma viremia timepoints between treated and untreated animals during the N-803 administration period, and no difference in the size of the viral DNA cell-associated reservoir post N-803 treatment. These results substantiate N-803 as a potent immunotherapeutic candidate capable of activating and directing effector CD8+ T and NK cells to the B cell follicle during full ART suppression, and suggest N-803 must be paired with a bona fide latency reversing agent in vivo to facilitate immune-mediated modulation of the latent viral reservoir.
Identifiants
pubmed: 32163523
doi: 10.1371/journal.ppat.1008339
pii: PPATHOGENS-D-19-01864
pmc: PMC7093032
doi:
Substances chimiques
ALT-803
0
Anti-Retroviral Agents
0
IL15 protein, human
0
Interleukin-15
0
Proteins
0
Recombinant Fusion Proteins
0
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
e1008339Subventions
Organisme : NIH HHS
ID : P51 OD011092
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI129703
Pays : United States
Organisme : NIH HHS
ID : K01 OD026561
Pays : United States
Organisme : NIAID NIH HHS
ID : R21 AI128970
Pays : United States
Organisme : NIAID NIH HHS
ID : HHSN272201800003C
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI140888
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI126617
Pays : United States
Déclaration de conflit d'intérêts
I have read the journal's policy and the authors of this manuscript have the following competing interests: Jeffrey Safrit is an employee of NantBioScience Inc./NantKWest LLC, the maker of N-803. Shiho Tanaka is an employee of ImmunityBio, a branch of NantKWest responsible for performing the ADA assay. No other authors have declared that competing interests exist.
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