Evidence map›Paper›PMID 33658029›Full record

ArticleJournal of nanobiotechnology2021

Nanotechnology against human cytomegalovirus in vitro: polyanionic carbosilane dendrimers as antiviral agents.

I Relaño-Rodríguez, M S Espinar-Buitrago, V Martín-Cañadilla, R Gómez-Ramirez, J L Jiménez, M A Muñoz-Fernández

Open access · goldAbstract read
In one paragraph

Article in Journal of nanobiotechnology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed, 14 citations in OpenAlex.

  1. Review
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  3. Article
  4. Review
  5. Prevention ofPharmaceutics · 2022
    Article
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

6 authors at 2 institutions in 1 country.

I Relaño-RodríguezSection Head Immunology, Laboratorio InmunoBiología Molecular, Hospital General Universitario Gregorio Marañón (HGUGM), Madrid, Spain.
M S Espinar-BuitragoSection Head Immunology, Laboratorio InmunoBiología Molecular, Hospital General Universitario Gregorio Marañón (HGUGM), Madrid, Spain.
V Martín-CañadillaSection Head Immunology, Laboratorio InmunoBiología Molecular, Hospital General Universitario Gregorio Marañón (HGUGM), Madrid, Spain.
R Gómez-RamirezDepartamento de Química Orgánica y Química Inorgánica, Universidad de Alcalá, Instituto de Investigación Química "Andrés M. del Río" (IQAR), UAH, Alcalá de Henares, 28871, Spain.
J L JiménezSection Head Immunology, Laboratorio InmunoBiología Molecular, Hospital General Universitario Gregorio Marañón (HGUGM), Madrid, Spain.
M A Muñoz-FernándezSection Head Immunology, Laboratorio InmunoBiología Molecular, Hospital General Universitario Gregorio Marañón (HGUGM), Madrid, Spain. mmunoz.hgugm@gmail.com.ORCID https://orcid.org/0000-0002-0813-4500
Hospital General Universitario Gregorio Marañón · ESUniversidad de Alcalá · ES

Funding

Comunidad de Madrid B2017/BMD-3703Comunidad de Madrid PEJ-2018-TL/BMD-11529Comunidad de Madrid PEJD-2019-PRE/IND-16567European Cooperation in Science and Technology OST Action CA 17140 "Cancer Nanomedicine from the Bench to the Bedside"IISGM COV20/MAM-BISInstituto de Salud Carlos III CIBER-BBNInstituto de Salud Carlos III PI16/01863Instituto de Salud Carlos III PI17/01115Instituto de Salud Carlos III PI19/01638Instituto de Salud Carlos III PT17/0015/0042Instituto de Salud Carlos III RD16/0025/0019PENTA FOUNDATION EPIICAL ProjectUniwersytet Medyczny w Lodzi NAWA International Academic Partnership Programme
6 · The paper itself

Abstract

backgroundHuman cytomegalovirus (HCMV) is a worldwide infection, causing different troublesome in immunosupressed patients and very related to Human Immunodeficiency Virus 1 (HIV-1) infection, mainly in developing countries, with a co-infection rate of 80% in Africa. The high cost of present treatments and the lack of routinely tests in these countries urge the necessity to develop new molecules or strategies against HCMV. The new treatments should be low-cost and capable of avoiding the emerging problem of resistant virus. Nanoparticles play an important role in several viral infections. Our main focus is to study the potential activity of polyanionic carbosilane dendrimers (PDC), which are hyperbranched molecules with several sulfonate or sulfate groups in their periphery, against different viruses.

resultsWe studied the activity of G1-S4, G2-S16 and G2-S24P PDCs in MRC-5 cell line against HCMV infection by several plaque reduction assays. Our results show that dendrimers present good biocompatibility at the concentrations tested (1-50 µM) for 6 days in cell culture. Interestingly, both G2-S16 and G2-S24P showed a remarked inhibition at 10 µM against HCMV infection. Results on attachment and virucidal assays indicated that the inhibition was not directed to the virus or the virus-cell attachment. However, results of time of addition, showed a longer lasting activity of these dendrimers in comparison to ganciclovir, and the combination of G2-S16 or G2-S24P with ganciclovir increases the HCMV inhibition around 90 %.

conclusionsNanotechnology, in particular polyanionic carbosilane dendrimers, have proved their potential application against HCMV, being capable of inhibiting the infection by themselves or enhancing the activity of ganciclovir, the actual treatment. These compounds represent a low-cost approach to fight HCMV infections.

Indexed as

Anti-HIV AgentsAntiviral AgentsCell LineCytomegalovirusCytomegalovirus InfectionsDendrimersFibroblastsGanciclovirHIV-1HIV InfectionsHumansNanotechnologyPolyelectrolytesSilanesAnti-HIV AgentsAntiviral AgentscarbosilaneDendrimersGanciclovirPolyelectrolytesSilanesGanciclovirHCMVPolyanionic carbosilane dendrimers

Identifiers

PMID33658029
PMCPMC7927225
OpenAlexW3133559052

What Socratic 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 Socratic graph.