Evidence map›Paper›PMID 34283885›Full record

ArticlePLoS pathogens2021

Improved delivery of broadly neutralizing antibodies by nanocapsules suppresses SHIV infection in the CNS of infant rhesus macaques.

Jing Wen, Tracy Cheever, Lan Wang, Di Wu, Jason Reed, John Mascola, Xuejun Chen, Cuiping Liu, Amarendra Pegu, Jonah B Sacha and 3 more

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.3field-weighted citation impact, top 23% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 14 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 4 institutions in 1 country.

Jing WenDepartment of Microbiology, Immunology and Molecular Genetics, David Geffen School of Medicine, University of California Los Angeles (UCLA), UCLA AIDS Institute, Los Angeles, California, United States of America.ORCID 0000-0002-6127-6276
Tracy CheeverOregon National Primate Research Center, Oregon Health & Science University, Beaverton, Oregon, United States of America.ORCID 0000-0002-2378-0690
Lan WangDepartment of Microbiology, Immunology and Molecular Genetics, David Geffen School of Medicine, University of California Los Angeles (UCLA), UCLA AIDS Institute, Los Angeles, California, United States of America.
Di WuDepartment of Chemical and Biomolecular Engineering, School of Engineering, UCLA, Los Angeles, California, United States of America.ORCID 0000-0002-3238-6388
Jason ReedVaccine & Gene Therapy Institute, Oregon Health & Science University, Beaverton, Oregon, United States of America.
John MascolaVaccine Research Center, National Institute of Allergy and Infectious Diseases, NIH, Bethesda Maryland, United States of America.ORCID 0000-0002-5293-4695
Xuejun ChenVaccine Research Center, National Institute of Allergy and Infectious Diseases, NIH, Bethesda Maryland, United States of America.ORCID 0000-0001-9192-0440
Cuiping LiuVaccine Research Center, National Institute of Allergy and Infectious Diseases, NIH, Bethesda Maryland, United States of America.
Amarendra PeguVaccine Research Center, National Institute of Allergy and Infectious Diseases, NIH, Bethesda Maryland, United States of America.ORCID 0000-0003-3564-6453
Jonah B SachaOregon National Primate Research Center, Oregon Health & Science University, Beaverton, Oregon, United States of America.
Yunfeng LuDepartment of Chemical and Biomolecular Engineering, School of Engineering, UCLA, Los Angeles, California, United States of America.
Nancy L HaigwoodOregon National Primate Research Center, Oregon Health & Science University, Beaverton, Oregon, United States of America.
Irvin S Y ChenDepartment of Microbiology, Immunology and Molecular Genetics, David Geffen School of Medicine, University of California Los Angeles (UCLA), UCLA AIDS Institute, Los Angeles, California, United States of America.ORCID 0000-0003-1199-2415
University of California, Los Angeles · USNational Institute of Allergy and Infectious Diseases · USOregon National Primate Research Center · USOregon Health & Science University · US

Funding

Upgrade of confocal microscopy at the Oregon National Primate Research CenterP51OD011092 · OD · OREGON HEALTH & SCIENCE UNIVERSITY · PI Bonnie J. Nagel · 2012 to 2026
$203.9M
Virology CoreP30AI028697 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI KITCHEN, SCOTT G · 1991 to 2018
$39.9M
HIV/AIDS Vaccine and Antibody DevelopmentZICAI005002 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI CHENG, CHENG · 2019 to 2025
$17.6M
Reducing Latent Viral Reservoirs in Infant MacaquesR01HD080459 · NICHD · OREGON HEALTH & SCIENCE UNIVERSITY · PI HAIGWOOD, NANCY L · 2014 to 2024
$10.2M
In Vivo Gene Editing for HIV-1 CureR01AI145038 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI CHEN, IRVIN S.Y. · 2019 to 2023
$3.4M
Targeting delivery of mAbs to CNS metastasesR01CA253215 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI WEN, JING · 2020 to 2024
$1.7M
Gene engineering using CRISPR/Cas9 mutagenesis to eliminate latent HIV-1R21AI114433 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI CHEN, IRVIN S.Y. · 2014 to 2015
$424k
NCI NIH HHS R01 CA253215NIAID NIH HHS P30 AI028697NIAID NIH HHS R01 AI145038NIAID NIH HHS R21 AI114433NICHD NIH HHS R01 HD080459NIH HHS P51 OD011092
6 · The paper itself

Abstract

Broadly neutralizing antibodies (bNAbs) directed to HIV-1 have shown promise at suppressing viremia in animal models. However, the use of bNAbs for the central nervous system (CNS) infection is confounded by poor penetration of the blood brain barrier (BBB). Typically, antibody concentrations in the CNS are extremely low; with levels in cerebrospinal fluid (CSF) only 0.1% of blood concentrations. Using a novel nanotechnology platform, which we term nanocapsules, we show effective transportation of the human bNAb PGT121 across the BBB in infant rhesus macaques upon systemic administration up to 1.6% of plasma concentration. We demonstrate that a single dose of PGT121 encased in nanocapsules when delivered at 48h post-infection delays early acute infection with SHIVSF162P3 in infants, with one of four animals demonstrating viral clearance. Importantly, the nanocapsule delivery of PGT121 improves suppression of SHIV infection in the CNS relative to controls.

Indexed as

AnimalsAnimals, NewbornAntibodies, ViralBlood-Brain BarrierBrainBroadly Neutralizing AntibodiesHumansMacaca mulattaNanocapsulesSimian Acquired Immunodeficiency SyndromeSimian Immunodeficiency VirusViral LoadAntibodies, ViralBroadly Neutralizing AntibodiesNanocapsules

Identifiers

PMID34283885
PMCPMC8323878
OpenAlexW3185972620

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.