Evidence map›Paper›PMID 1309271›Full record

ArticleVirology1992

MHV S peplomer protein expressed by a recombinant vaccinia virus vector exhibits IgG Fc-receptor activity.

E L Oleszak, S Perlman, J L Leibowitz

Open access · greenAbstract read
In one paragraph

Article in Virology, 1992. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

17 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Article
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  4. Antigenicity and receptor-binding ability of recombinant SARS coronavirus spike protein.Biochemical and biophysical research communications · 2004
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  5. Review
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  10. The molecular biology of coronaviruses.Advances in virus research · 1997
    Review
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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

3 authors at 1 institution in 1 country.

E L OleszakDepartment of Pathology and Laboratory Medicine, University of Texas Health Science Center, Houston 77030.
S Perlman
J L Leibowitz
The University of Texas Health Science Center at Houston · US

Funding

ANTIBODY-MODULATED DEMYELINATIONK04NS001369 · NINDS · UNIVERSITY OF IOWA · PI PERLMAN, STANLEY · 1989 to 1993
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PATHOGENESIS OF ANTIBODY-MODULATED JHM DEMYELINATIONR01NS024401 · NINDS · UNIVERSITY OF IOWA · PI PERLMAN, STANLEY · 1987 to 1994
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NINDS NIH HHS NS 01369NINDS NIH HHS NS 24401
6 · The paper itself

Abstract

We have previously shown that cells infected with mouse hepatitis virus (MHV) bind rabbit, mouse, and rat IgG by the Fc portion of the IgG molecule. This Fc-binding activity appeared to be mediated by the MHV S protein. S protein could also be precipitated from MHV-infected cells by a monoclonal antibody directed against the murine Fc gamma receptor (Fc gamma R). To prove definitively that the S protein mediates Fc-binding activity, we have expressed the MHV S protein utilizing recombinant vaccinia viruses. The anti-Fc gamma R monoclonal antibody, 2.4G2, precipitated recombinant S protein in cells of murine, human, and rabbit origin. Since the anti-Fc receptor monoclonal antibody does not react with human and rabbit Fc receptors these results demonstrate that the epitope recognized by this antibody is carried on the MHV S protein and is not murine in origin. Examination of various MHV isolates and escape mutants failed to identify the precise sequences in S responsible for the molecular mimicry of the murine Fc gamma R. These data are consistent with the hypothesis that a previously identified region of similarity between the S protein and the Fc gamma R mediates this activity. The Fc binding activity of S was expressed on the cell surface, since MHV-JHM-infected cells, but not uninfected cells, formed rosettes with anti-sheep red blood cell (SRBC) antibody-coated SRBC. The anti-Fc gamma R monoclonal antibody neutralized MHV-JHM and inhibited syncytium formation induced by the MHV S protein.

Indexed as

Membrane GlycoproteinsAnimalsAntibodies, MonoclonalAntigens, DifferentiationCells, CulturedCross ReactionsDNA Mutational AnalysisHumansImmunoglobulin Fc FragmentsMurine hepatitis virusNeutralization TestsReceptors, FcReceptors, IgGRecombinant ProteinsSpike Glycoprotein, CoronavirusStructure-Activity RelationshipAntibodies, MonoclonalAntigens, DifferentiationImmunoglobulin Fc FragmentsMembrane GlycoproteinsReceptors, FcReceptors, IgGRecombinant ProteinsSpike Glycoprotein, Coronavirusspike glycoprotein, SARS-CoVspike protein, mouse hepatitis virusViral Envelope ProteinsViral Fusion ProteinsViral Matrix Proteins

Identifiers

PMID1309271
PMCPMC7131518
OpenAlexW1991569048

What OpenQuestion holds

Textmetadata
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.