Evidence map›Paper›PMID 23049856›Full record

ArticlePloS one2012

Specific acquisition of functional CD59 but not CD46 or CD55 by hepatitis C virus.

Asim Ejaz, Eike Steinmann, Zoltán Bánki, Anggakusuma, Sana Khalid, Susanne Lengauer, Corinne Wilhelm, Heinz Zoller, Anna Schloegl, Joerg Steinmann and 4 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2012. 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
0.9field-weighted citation impact, top 27% 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, 21 citations in OpenAlex.

  1. Article
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  3. Interactions of viruses and the humoral innate immune response.Clinical immunology (Orlando, Fla.) · 2020
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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

14 authors at 4 institutions in 2 countries.

Asim EjazInstitute of Virology, Innsbruck Medical University, Innsbruck, Austria.
Eike Steinmann
Zoltán Bánki
Anggakusuma
Sana Khalid
Susanne Lengauer
Corinne Wilhelm
Heinz Zoller
Anna Schloegl
Joerg Steinmann
Elena Grabski
Michael Kleines
Thomas Pietschmann
Heribert Stoiber
Innsbruck Medical University · ATCenter for Experimental and Clinical Infection Research · DEUniversity Hospital Innsbruck · ATEssen University Hospital · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Viruses of different families encode for regulators of the complement system (RCAs) or acquire such RCAs from the host to get protection against complement-mediated lysis (CML). As hepatitis C virus (HCV) shares no genetic similarity to any known RCA and is detectable at high titers in sera of infected individuals, we investigated whether HCV has adapted host-derived RCAs to resist CML. Here we report that HCV selectively incorporates CD59 while neither CD55, nor CD46 are associated with the virus. The presence of CD59 was shown by capture assays using patient- and cell culture-derived HCV isolates. Association of CD59 with HCV was further confirmed by Western blot analysis using purified viral supernatants from infected Huh 7.5 cells. HCV captured by antibodies specific for CD59 remained infectious for Huh 7.5 cells. In addition, blocking of CD59 in the presence of active complement reduced the titer of HCV most likely due to CML. HCV produced in CD59 knock-down cells were more significantly susceptible to CML compared to wild type virus, but neither replication, assembly nor infectivity of the virus seemed to be impaired in the absence of CD59. In summary our data indicate that HCV incorporates selectively CD59 in its envelope to gain resistance to CML in serum of infected individuals.

Indexed as

AdultAgedCD55 AntigensCD59 AntigensCell LineCell Line, TumorComplement ActivationComplement Inactivator ProteinsComplement System ProteinsFemaleFlow CytometryGenotypeHepacivirusHumansImmunoglobulin GMaleCD55 AntigensCD59 AntigensComplement Inactivator ProteinsComplement System ProteinsImmunoglobulin GMembrane Cofactor Protein

Identifiers

PMID23049856
PMCPMC3458075
OpenAlexW1980138364

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.