Evidence map›Paper›PMID 32664555›Full record

ArticlePharmaceutics2020

Nanoparticle-Delivered HIV Peptides to Dendritic Cells a Promising Approach to Generate a Therapeutic Vaccine.

Alba Martín-Moreno, José L Jiménez Blanco, Jamie Mosher, Douglas R Swanson, José M García Fernández, Ajit Sharma, Valentín Ceña, María Angeles Muñoz-Fernández

Open access · goldAbstract read
In one paragraph

Article in Pharmaceutics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.5field-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

4 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Review
  3. Cyclodextrin-Based Functional Glyconanomaterials.Nanomaterials (Basel, Switzerland) · 2020
    Review
  4. Nanosystems Applied to HIV Infection: Prevention and Treatments.International journal of molecular sciences · 2020
    Review
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

8 authors at 5 institutions in 2 countries.

Alba Martín-MorenoSection of Immunology, ImmunoBiology Molecular Laboratory, Spanish HIV HGM BioBank, Hospital General Universitario Gregorio Marañón, 28007 Madrid, Spain.
José L Jiménez BlancoDepartment of. Química Orgánica, Facultad de Química, Universidad de Sevilla, 41012 Sevilla, Spain.
Jamie MosherDepartment of Chemistry & Biochemistry, Central Michigan University, Mount Pleasant, MI 48859, USA.
Douglas R SwansonDepartment of Chemistry & Biochemistry, Central Michigan University, Mount Pleasant, MI 48859, USA.
José M García FernándezInstitute for Chemical Research, CSIC-University of Sevilla, 41092 Sevilla, Spain.
Ajit SharmaDepartment of Chemistry & Biochemistry, Central Michigan University, Mount Pleasant, MI 48859, USA.
Valentín CeñaCIBERNED, Instituto de Salud Carlos III, 28031 Madrid, Spain.
María Angeles Muñoz-FernándezSection of Immunology, ImmunoBiology Molecular Laboratory, Spanish HIV HGM BioBank, Hospital General Universitario Gregorio Marañón, 28007 Madrid, Spain.
Central Michigan University · USInstituto de Salud Carlos III · ESHospital General Universitario Gregorio Marañón · ESInstituto de Investigaciones Químicas · ESUniversidad de Sevilla · ES

Funding

Comunidad de Madrid B2017/BMD-3703European Cooperation in Science and Technology CA 17140Instituto de Salud Carlos III PI16/01863Instituto de Salud Carlos III PI17/01115Instituto de Salud Carlos III PI17CIII/00003Instituto de Salud Carlos III RD16/0002/0006Instituto de Salud Carlos III RD16/0025/0019Instituto de Salud Carlos III RD16CIII/0002/0002Instituto de Salud Carlos III RETIC PT17/0015/0042Junta de Comunidades de Castilla-La Mancha SBPLY/19/180501/000067MICIU RTI2018097609-B-C21Ministerio de Economía, Industria y Competitividad, Gobierno de España 2016-76083-RMinisterio de Economía, Industria y Competitividad, Gobierno de España SAF2017-89288-RNarodowa Agencja Wymiany Akademickiej International Academic Partnership ProgrammeNIH HHS 1R21EY030012-01
6 · The paper itself

Abstract

Finding a functional cure for HIV-1 infection will markedly decrease the social and economic burden of this disease. In this work, we have taken advantage of the antigen presenting cell role of human dendritic cells (DCs) to try to induce an immune response to HIV-derived peptide delivered to DCs using two different polycationic nanoparticles: a G4 PAMAM dendrimer modified to a 70/30 ratio of hydroxyl groups/amines and a cyclodextrin derivative. We have studied peptide delivery using a fluorescence peptide and have studied the immune response generation by cytokine determination and flow cytometry. We have found a robust delivery of the antigenic peptide to DCs and activated dendritic cell-mediated peripheral blood mononuclear cells (PBMCs) proliferation using the mixed lymphocyte reaction. However, no expression of markers indicating activation of either B or T lymphocytes was observed. Moreover, the release of the pro-inflammatory cytokine TNF-α or IL-2 was only observed when DCs treated with either the dendrimer or the dendriplex containing the peptide. Antigenic peptide delivery to DCs is a promising approach to generate a vaccine against HIV-1 infection. However, more studies, including the simultaneous delivery of several antigenic peptides from different viral proteins, can markedly improve the immune response.

Indexed as

cytokinesDCsdeliveryfluorescence peptidesHIV-1polycationic nanoparticlesvaccine

Identifiers

PMID32664555
PMCPMC7407655
OpenAlexW3041290879

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.