Evidence map›Paper›PMID 28792942›Full record

ArticlePloS one2017

HIV-1-neutralizing antibody induced by simian adenovirus- and poxvirus MVA-vectored BG505 native-like envelope trimers.

Silvia Capucci, Edmund G Wee, Torben Schiffner, Celia C LaBranche, Nicola Borthwick, Albert Cupo, Jonathan Dodd, Hansi Dean, Quentin Sattentau, David Montefiori and 4 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.7field-weighted citation impact, top 18% 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

13 citing papers in PubMed, 16 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 4 institutions in 5 countries.

Silvia CapucciThe Jenner Institute, University of Oxford, Oxford, United Kingdom.
Edmund G WeeThe Jenner Institute, University of Oxford, Oxford, United Kingdom.
Torben SchiffnerThe Sir William Dunn School of Pathology, University of Oxford, Oxford, United Kingdom.
Celia C LaBrancheDepartment of Surgery, Duke University Medical Center, Durham, North Carolina, United States of America.
Nicola BorthwickThe Jenner Institute, University of Oxford, Oxford, United Kingdom.
Albert CupoDepartment of Microbiology and Immunology, Weill Cornell Medical College, New York, New York, United States of America.
Jonathan DoddThe Sir William Dunn School of Pathology, University of Oxford, Oxford, United Kingdom.
Hansi DeanThe International AIDS Vaccine Initiative, New York, New York, United States of America.
Quentin SattentauThe Sir William Dunn School of Pathology, University of Oxford, Oxford, United Kingdom.
David MontefioriDepartment of Surgery, Duke University Medical Center, Durham, North Carolina, United States of America.
Per J KlasseDepartment of Microbiology and Immunology, Weill Cornell Medical College, New York, New York, United States of America.
Rogier W SandersDepartment of Microbiology and Immunology, Weill Cornell Medical College, New York, New York, United States of America.
John P MooreDepartment of Microbiology and Immunology, Weill Cornell Medical College, New York, New York, United States of America.
Tomáš HankeThe Jenner Institute, University of Oxford, Oxford, United Kingdom.ORCID http://orcid.org/0000-0002-6076-9546
University of Oxford · GBCornell University · USDuke Medical Center · USInternational AIDS Vaccine Initiative · US

Funding

Virus biology scientific research support componentUM1AI100645 · NIAID · DUKE UNIVERSITY · PI MCMICHAEL, ANDREW JAMES · 2012 to 2018
$204.7M
Structural studies of native-like SOSIP trimersP01AI110657 · NIAID · WEILL MEDICAL COLL OF CORNELL UNIV · PI MOORE, JOHN P · 2015 to 2024
$35.4M
Medical Research Council G0000635Medical Research Council G1001757Medical Research Council MR/N023668/1NIAID NIH HHS P01 AI110657NIAID NIH HHS UM1 AI100645
6 · The paper itself

Abstract

Rabbits and monkeys immunized with HIV type 1 (HIV-1) native-like BG505 SOSIP.664 (BG505s) glycoprotein trimers are known to induce antibodies that can neutralize the autologous tier-2 virus. Here, we assessed the induction of HIV-1 trimer binding and neutralizing antibody (nAb) titres when BG505s trimers were also delivered by non-replicating simian (chimpanzee) adenovirus and non-replicating poxvirus modified vaccinia virus Ankara (MVA) vaccine vectors. First, we showed that approximately two-thirds and one-third of the trimers secreted from the ChAdOx1.BG505s (C) and MVA.BG505s (M) vaccine-infected cells, respectively, were cleaved and in a native-like conformation. Rabbits were immunized intramuscularly with these vaccine vectors and in some cases boosted with ISCOMATRIX™-adjuvanted BG505s protein trimer (P), using CCC, MMM, PPP, CPP, MPP and CMP vaccine regimens. We found that the peak trimer-binding antibody and tier-1A and autologous tier-2 nAb responses induced by the CC, CM, PPP, CPP, MPP and CMP regimens were comparable, although only PPP induced autologous tier-2 nAbs in all the immunized animals. Three animals developed weak heterologous tier-2 nAbs. These results demonstrate that ChAdOx1 and MVA vectors are useful delivery modalities for not only T-cell, but also antibody vaccine development.

Indexed as

Adenoviruses, SimianAIDS VaccinesAnimalsAntibodies, NeutralizingCell Lineenv Gene Products, Human Immunodeficiency VirusHEK293 CellsHIV-1HIV AntibodiesHumansProtein MultimerizationRabbitsVaccinationVaccines, DNAVaccinia virusViral VaccinesAIDS VaccinesAntibodies, Neutralizingenv Gene Products, Human Immunodeficiency VirusHIV AntibodiesMVA vaccineVaccines, DNAViral Vaccines

Identifiers

PMID28792942
PMCPMC5549892
OpenAlexW2743135312

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.