Evidence map›Paper›PMID 27314381›Full record

ArticleViruses2016

Identification of Vimentin as a Potential Therapeutic Target against HIV Infection.

Celia Fernández-Ortega, Anna Ramírez, Dionne Casillas, Taimi Paneque, Raimundo Ubieta, Marta Dubed, Leonor Navea, Lila Castellanos-Serra, Carlos Duarte, Viviana Falcon and 7 more

Open access · goldAbstract read
In one paragraph

Article in Viruses, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

18 citing papers in PubMed, 40 citations in OpenAlex.

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  13. Vimentin as a target for the treatment of COVID-19.BMJ open respiratory research · 2020
    Article
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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

17 authors at 1 institution in 1 country.

Celia Fernández-OrtegaCenter for Genetic Engineering and Biotechnology, Ave 31/158 and 190, Cubanacán, Playa, P.O. Box 6162, Havana 10600, Cuba. celia.fernandez@cigb.edu.cu.
Anna RamírezCenter for Genetic Engineering and Biotechnology, Ave 31/158 and 190, Cubanacán, Playa, P.O. Box 6162, Havana 10600, Cuba. anna.ramirez@cigb.edu.cu.
Dionne CasillasCenter for Genetic Engineering and Biotechnology, Ave 31/158 and 190, Cubanacán, Playa, P.O. Box 6162, Havana 10600, Cuba. dionne.casillas@cigb.edu.cu.
Taimi PanequeCenter for Genetic Engineering and Biotechnology, Ave 31/158 and 190, Cubanacán, Playa, P.O. Box 6162, Havana 10600, Cuba. taimi.paneque@cigb.edu.cu.
Raimundo UbietaCenter for Genetic Engineering and Biotechnology, Ave 31/158 and 190, Cubanacán, Playa, P.O. Box 6162, Havana 10600, Cuba. raimundo.ubieta@cigb.edu.cu.
Marta DubedLaboratory for AIDS Research, Carretera de Tapaste y Autopista Nacional, San José de las Lajas, Mayabeque CP 32700, Cuba. cicdc@infomed.sld.cu.
Leonor NaveaLaboratory for AIDS Research, Carretera de Tapaste y Autopista Nacional, San José de las Lajas, Mayabeque CP 32700, Cuba. riverora@infomed.sld.cu.
Lila Castellanos-SerraCenter for Genetic Engineering and Biotechnology, Ave 31/158 and 190, Cubanacán, Playa, P.O. Box 6162, Havana 10600, Cuba. lilacastellanos@infomed.sld.cu.
Carlos DuarteCenter for Genetic Engineering and Biotechnology, Ave 31/158 and 190, Cubanacán, Playa, P.O. Box 6162, Havana 10600, Cuba. carlos.duarte@cigb.edu.cu.
Viviana FalconCenter for Genetic Engineering and Biotechnology, Ave 31/158 and 190, Cubanacán, Playa, P.O. Box 6162, Havana 10600, Cuba. viviana.falcon@cigb.edu.cu.
Osvaldo ReyesCenter for Genetic Engineering and Biotechnology, Ave 31/158 and 190, Cubanacán, Playa, P.O. Box 6162, Havana 10600, Cuba. osvaldo.reyes@cigb.edu.cu.
Hilda GarayCenter for Genetic Engineering and Biotechnology, Ave 31/158 and 190, Cubanacán, Playa, P.O. Box 6162, Havana 10600, Cuba. hilda.garay@cigb.edu.cu.
Eladio SilvaLaboratory for AIDS Research, Carretera de Tapaste y Autopista Nacional, San José de las Lajas, Mayabeque CP 32700, Cuba. eladio.silva@infomed.sld.cu.
Enrique NoaLaboratory for AIDS Research, Carretera de Tapaste y Autopista Nacional, San José de las Lajas, Mayabeque CP 32700, Cuba. enrnoa@infomed.sld.cu.
Yassel RamosCenter for Genetic Engineering and Biotechnology, Ave 31/158 and 190, Cubanacán, Playa, P.O. Box 6162, Havana 10600, Cuba. yassel.ramos@cigb.edu.cu.
Vladimir BesadaCenter for Genetic Engineering and Biotechnology, Ave 31/158 and 190, Cubanacán, Playa, P.O. Box 6162, Havana 10600, Cuba. vladimir.besada@cigb.edu.cu.
Lázaro BetancourtCenter for Genetic Engineering and Biotechnology, Ave 31/158 and 190, Cubanacán, Playa, P.O. Box 6162, Havana 10600, Cuba. lazaro.betancourt@cigb.edu.cu.
Centro de Ingeniería Genética y Biotecnología · CU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A combination of antiviral drugs known as antiretroviral therapy (ART) has shown effectiveness against the human immunodeficiency virus (HIV). ART has markedly decreased mortality and morbidity among HIV-infected patients, having even reduced HIV transmission. However, an important current disadvantage, resistance development, remains to be solved. Hope is focused on developing drugs against cellular targets. This strategy is expected to prevent the emergence of viral resistance. In this study, using a comparative proteomic approach in MT4 cells treated with an anti-HIV leukocyte extract, we identified vimentin, a molecule forming intermediate filaments in the cell, as a possible target against HIV infection. We demonstrated a strong reduction of an HIV-1 based lentivirus expressing the enhanced green fluorescent protein (eGFP) in vimentin knockdown cells, and a noteworthy decrease of HIV-1 capsid protein antigen (CAp24) in those cells using a multiround infectivity assay. Electron micrographs showed changes in the structure of intermediate filaments when MT4 cells were treated with an anti-HIV leukocyte extract. Changes in the structure of intermediate filaments were also observed in vimentin knockdown MT4 cells. A synthetic peptide derived from a cytoskeleton protein showed potent inhibitory activity on HIV-1 infection, and low cytotoxicity. Our data suggest that vimentin can be a suitable target to inhibit HIV-1.

Indexed as

Drug DiscoveryHost-Pathogen InteractionsVirus ReplicationAnti-HIV AgentsCell LineGene Knockdown TechniquesHIV-1HIV Core Protein p24HIV InfectionsHumansVimentinAnti-HIV AgentsHIV Core Protein p24Vimentinanti-HIV activitycytoskeletonHIVintermediate filamentsleukocyte extractproteomicsvimentin

Identifiers

PMID27314381
PMCPMC4926169
OpenAlexW2443329401

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.