Evidence map›Paper›PMID 31852794›Full record

ArticleJournal of virology2020

Neutralizing Antibody Induction by HIV-1 Envelope Glycoprotein SOSIP Trimers on Iron Oxide Nanoparticles May Be Impaired by Mannose Binding Lectin.

Rajesh P Ringe, Victor M Cruz Portillo, Pia Dosenovic, Thomas J Ketas, Gabriel Ozorowski, Bartek Nogal, Lautaro Perez, Celia C LaBranche, Jillian Lim, Erik Francomano and 8 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of virology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

25 citing papers in PubMed, 37 citations in OpenAlex.

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  5. Modulation of immune responses to liposomal vaccines by intrastructural help.European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V · 2023
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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

18 authors at 5 institutions in 2 countries.

Rajesh P RingeDepartment of Microbiology and Immunology, Weill Cornell Medical College, New York, New York, USA.
Victor M Cruz PortilloDepartment of Microbiology and Immunology, Weill Cornell Medical College, New York, New York, USA.
Pia DosenovicLaboratory of Molecular Immunology, The Rockefeller University, New York, New York, USA.
Thomas J KetasDepartment of Microbiology and Immunology, Weill Cornell Medical College, New York, New York, USA.
Gabriel OzorowskiDepartment of Integrative Structural and Computational Biology, Consortium for HIV Vaccine Development (CHAVD), The Scripps Research Institute, La Jolla, California, USA.ORCID 0000-0002-9695-8138
Bartek NogalDepartment of Integrative Structural and Computational Biology, Consortium for HIV Vaccine Development (CHAVD), The Scripps Research Institute, La Jolla, California, USA.
Lautaro PerezDuke University Medical Center, Durham, North Carolina, USA.
Celia C LaBrancheDuke University Medical Center, Durham, North Carolina, USA.ORCID 0000-0002-6653-6655
Jillian LimDepartment of Microbiology and Immunology, Weill Cornell Medical College, New York, New York, USA.
Erik FrancomanoDepartment of Microbiology and Immunology, Weill Cornell Medical College, New York, New York, USA.
Ian A WilsonDepartment of Integrative Structural and Computational Biology, Consortium for HIV Vaccine Development (CHAVD), The Scripps Research Institute, La Jolla, California, USA.
Rogier W SandersDepartment of Microbiology and Immunology, Weill Cornell Medical College, New York, New York, USA.
Andrew B WardDepartment of Integrative Structural and Computational Biology, Consortium for HIV Vaccine Development (CHAVD), The Scripps Research Institute, La Jolla, California, USA.
David C MontefioriDuke University Medical Center, Durham, North Carolina, USA.
Michel C NussenzweigLaboratory of Molecular Immunology, The Rockefeller University, New York, New York, USA.
P J KlasseDepartment of Microbiology and Immunology, Weill Cornell Medical College, New York, New York, USA.
Albert CupoDepartment of Microbiology and Immunology, Weill Cornell Medical College, New York, New York, USA.
John P MooreDepartment of Microbiology and Immunology, Weill Cornell Medical College, New York, New York, USA jpm2003@med.cornell.edu.
Cornell University · USScripps Research Institute · USDuke Medical Center · USHoward Hughes Medical Institute · USRockefeller University · US

Funding

Structural studies of native-like SOSIP trimersP01AI110657 · NIAID · WEILL MEDICAL COLL OF CORNELL UNIV · PI MOORE, JOHN P · 2015 to 2024
$35.4M
Neutralization of Primate Immunodeficiency VirusesR01AI036082 · NIAID · WEILL MEDICAL COLL OF CORNELL UNIV · PI JOHN P MOORE · 1994 to 2026
$4.3M
New Approaches for Vaccine Development against HIVK99AI127243 · NIAID · ROCKEFELLER UNIVERSITY · PI DOSENOVIC, PIA KAROLIN · 2017 to 2018
$284k
Howard Hughes Medical InstituteNIAID NIH HHS K99 AI127243NIAID NIH HHS P01 AI110657NIAID NIH HHS R01 AI036082
6 · The paper itself

Abstract

We covalently attached human immunodeficiency virus type 1 (HIV-1) Env SOSIP trimers to iron oxide nanoparticles (IO-NPs) to create a particulate immunogen for neutralizing antibody (NAb) induction. The attached trimers, ∼20 per particle, retained native-like antigenicity, judged by reactivity with NAbs and non-NAbs. Bivalent (BG505 and B41) trimer IO-NPs were made, as were IO-NPs displaying B41 trimers carrying a PADRE T-cell helper epitope (TCHE). We immunized mice with B41 soluble or IO-NP trimers after PADRE peptide priming. After two immunizations, IO-NP presentation and the TCHE tag independently and substantially increased anti-trimer antibody responses, but titer differences waned after two further doses. Notable and unexpected findings were that autologous NAbs to the N289 glycan hole epitope were consistently induced in mice given soluble but not IO-NP trimers. Various recombinant mannose binding lectins (MBLs) and MBLs in sera of both murine and human origin bound to soluble and IO-NP trimers. MBL binding occluded the autologous NAb epitope on the B41 IO-NP trimers, which may contribute to its poor immunogenicity. The exposure of a subset of broadly active NAb epitopes was also impaired by MBL binding, which could have substantial implications for the utility of trimer-bearing nanoparticles in general and perhaps also for soluble Env proteins.

Indexed as

Magnetite NanoparticlesAnimalsAntibodies, Neutralizingenv Gene Products, Human Immunodeficiency VirusEpitopes, T-LymphocyteHIV-1HIV AntibodiesHumansMannose-Binding LectinMiceProtein MultimerizationAntibodies, Neutralizingenv Gene Products, Human Immunodeficiency VirusEpitopes, T-LymphocyteHIV AntibodiesMagnetite NanoparticlesMannose-Binding LectinHIV-1 immunogensmannose binding lectinnanoparticlesneutralizing antibodiesSOSIP trimer

Identifiers

PMID31852794
PMCPMC7158715
OpenAlexW2995005180

What OpenQuestion holds

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Registered trials

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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.