Evidence map›Paper›PMID 31113488›Full record

ArticleJournal of nanobiotechnology2019

Polyanionic carbosilane dendrimers as a new adjuvant in combination with latency reversal agents for HIV treatment.

Ignacio Relaño-Rodríguez, Raquel Juárez-Sánchez, Carolina Pavicic, Eduardo Muñoz, Maria Ángeles Muñoz-Fernández

Open access · goldAbstract read
In one paragraph

Article in Journal of nanobiotechnology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

11 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. Review
  8. Nanosystems Applied to HIV Infection: Prevention and Treatments.International journal of molecular sciences · 2020
    Review
  9. Review
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  11. 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

5 authors at 2 institutions in 1 country.

Ignacio Relaño-RodríguezMolecular Immunology Laboratory, Hospital General Universitario Gregorio Marañón, Madrid, Spain.
Raquel Juárez-SánchezMolecular Immunology Laboratory, Hospital General Universitario Gregorio Marañón, Madrid, Spain.
Carolina PavicicInnohealth, Parque Científico de Madrid, Madrid, Spain.
Eduardo MuñozDepartment of Cell Biology, Physiology and Immunology, Instituto Maimónides de Investigaciones Biomédicas de Córdoba (IMIBIC)/Reina Sofia University Hospital University of Córdoba, Córdoba, Spain.
Maria Ángeles Muñoz-FernándezMolecular Immunology Laboratory, Hospital General Universitario Gregorio Marañón, Madrid, Spain. mmunoz.hgugm@gmail.com.ORCID http://orcid.org/0000-0002-0813-4500
Hospital General Universitario Gregorio Marañón · ESInstituto Maimónides de Investigación Biomédica de Córdoba · ES

Funding

European Cooperation in Science and Technology COST CA17140Instituto de Salud Carlos III CIBER-BBNInstituto de Salud Carlos III PI16/01863Instituto de Salud Carlos III PT17/0015/0042Instituto de Salud Carlos III RD16/0025/0019PENTA FOUNDATION EPIICAL Project
6 · The paper itself

Abstract

backgroundThe major obstacle impeding human immunodeficiency virus-1 (HIV-1) eradication in antiretroviral treatment (ART) treated HIV-1 subjects is the establishment of long-lived latently infected resting CD4

methodsJ89GFP lymphocyte and THP89GFP monocyte derived cell lines latently infected with HIV-1 p89GFP were used as an in vitro model of latency for our study. Viability assays by 3-(4-5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) and lactate dehydrogenase (LDH) were performed to determine the working concentrations of dendrimers and LRAs. Both cell lines were treated with G1-S4, G2-S16 and G3-S16 either alone or in combination with bryostatin (BRY), romidepsin (RMD) or panobinostat (PNB) for 24 and 48 h. The expression pattern of GFP was measured by flow cytometry and referred as measure of viral reactivation. RESULTS AND DISCUSSION: The combination treatment of the dendrimers with the protein kinase C (PKC) agonist did not modify the antilatency activity in J89GFP lymphocyte cell line. Interestingly enough, G3-S16 dendrimer alone and its combination with BRY, RMD or PNB showed a significant increased expression of GFP in the THP89GFP monocyte cell line.

conclusionWe showed for the first time that nanoparticles, in this case, G3-S16 anionic carbosilan dendrimer may play an important role in new treatments against HIV-1 infection.

Indexed as

Adjuvants, ImmunologicAnti-HIV AgentsBryostatinsCell LineCell SurvivalDendrimersDepsipeptidesDrug LiberationDrug Therapy, CombinationHIV-1HIV InfectionsHumansLymphocytesMonocytesPanobinostatParticle SizeAdjuvants, ImmunologicAnti-HIV Agentsbryostatin 1BryostatinscarbosilaneDendrimersDepsipeptidesPanobinostatPolyelectrolytesPolymersromidepsinSilanesDendrimersHIV-1 latencyLatency reversal agentsNanomedicine

Identifiers

PMID31113488
PMCPMC6529996
OpenAlexW2947527149

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.