Evidence map›Paper›PMID 30302284›Full record

ArticleNPJ vaccines2018

Overcoming immunogenicity issues of HIV p24 antigen by the use of innovative nanostructured lipid carriers as delivery systems: evidences in mice and non-human primates.

Emilie Bayon, Jessica Morlieras, Nathalie Dereuddre-Bosquet, Alexis Gonon, Leslie Gosse, Thomas Courant, Roger Le Grand, Patrice N Marche, Fabrice P Navarro

Open access · goldAbstract read
In one paragraph

Article in NPJ vaccines, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
5.8field-weighted citation impact, top 3% 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

8 citing papers in PubMed, 59 citations in OpenAlex.

  1. Article
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  3. Nanomedicine based approaches for combating viral infections.Journal of controlled release : official journal of the Controlled Release Society · 2021
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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

9 authors at 3 institutions in 1 country.

Emilie Bayon1Univ. Grenoble Alpes, F-38000 Grenoble, France.
Jessica Morlieras1Univ. Grenoble Alpes, F-38000 Grenoble, France.
Nathalie Dereuddre-Bosquet4Center for Immunology of Viral Infections and Autoimmune Diseases, IDMIT department, IBFJ, CEA, Université Paris Sud 11, INSERM U1184, 92265 Fontenay-aux-Roses, France.
Alexis Gonon1Univ. Grenoble Alpes, F-38000 Grenoble, France.
Leslie Gosse4Center for Immunology of Viral Infections and Autoimmune Diseases, IDMIT department, IBFJ, CEA, Université Paris Sud 11, INSERM U1184, 92265 Fontenay-aux-Roses, France.
Thomas Courant1Univ. Grenoble Alpes, F-38000 Grenoble, France.
Roger Le Grand4Center for Immunology of Viral Infections and Autoimmune Diseases, IDMIT department, IBFJ, CEA, Université Paris Sud 11, INSERM U1184, 92265 Fontenay-aux-Roses, France.
Patrice N Marche1Univ. Grenoble Alpes, F-38000 Grenoble, France.ORCID 0000-0002-8930-9340
Fabrice P Navarro1Univ. Grenoble Alpes, F-38000 Grenoble, France.
Institut polytechnique de Grenoble · FRUniversité Paris-Sud · FRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

HIV is one of the deadliest pandemics of modern times, having already caused 35 million deaths around the world. Despite the huge efforts spent to develop treatments, the virus cannot yet be eradicated and continues to infect new people. Spread of the virus remains uncontrolled, thus exposing the worldwide population to HIV danger, due to the lack of efficient vaccines. The latest clinical trials describe the challenges associated with developing an effective prophylactic HIV vaccine. These immunological obstacles will only be overcome by smart and innovative solutions applied to the design of vaccine formulations. Here, we describe the use of nanostructured lipid carriers (NLC) for the delivery of p24 protein as a model HIV antigen, with the aim of increasing its immunogenicity. We have designed vaccine formulations comprising NLC grafted with p24 antigen, together with cationic NLC optimized for the delivery of immunostimulant CpG. This tailored system significantly enhanced immune responses against p24, in terms of specific antibody production and T-cell activation in mice. More importantly, the capacity of NLC to induce specific immune responses against this troublesome HIV antigen was further supported by a 7-month study on non-human primates (NHP). This work paves the way toward the development of a future HIV vaccine, which will also require the use of envelope antigens.

Identifiers

PMID30302284
PMCPMC6167354
OpenAlexW2890298347

What OpenQuestion holds

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LicenceCC BY
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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.