Evidence map›Paper›PMID 28630325›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2017

Convergent immunological solutions to Argentine hemorrhagic fever virus neutralization.

Antra Zeltina, Stefanie A Krumm, Mehmet Sahin, Weston B Struwe, Karl Harlos, Jack H Nunberg, Max Crispin, Daniel D Pinschewer, Katie J Doores, Thomas A Bowden

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
3.1field-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

30 citing papers in PubMed, 36 citations in OpenAlex.

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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

10 authors at 7 institutions in 3 countries.

Antra ZeltinaDivision of Structural Biology, Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford OX3 7BN, United Kingdom.
Stefanie A KrummDepartment of Infectious Diseases, Guy's Hospital, King's College London, London SE1 9RT, United Kingdom.
Mehmet SahinDivision of Experimental Virology, Department of Biomedicine, University of Basel, Basel CH-4051, Switzerland.
Weston B StruweOxford Glycobiology Institute, Department of Biochemistry, University of Oxford, Oxford OX1 3QU, United Kingdom.
Karl HarlosDivision of Structural Biology, Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford OX3 7BN, United Kingdom.
Jack H NunbergMontana Biotechnology Center, University of Montana, Missoula, MT 59812.
Max CrispinOxford Glycobiology Institute, Department of Biochemistry, University of Oxford, Oxford OX1 3QU, United Kingdom.
Daniel D PinschewerDivision of Experimental Virology, Department of Biomedicine, University of Basel, Basel CH-4051, Switzerland.
Katie J DooresDepartment of Infectious Diseases, Guy's Hospital, King's College London, London SE1 9RT, United Kingdom; katie.doores@kcl.ac.uk thomas.bowden@strubi.ox.ac.uk.
Thomas A BowdenDivision of Structural Biology, Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford OX3 7BN, United Kingdom; katie.doores@kcl.ac.uk thomas.bowden@strubi.ox.ac.uk.
University of Oxford · GBUniversity of Basel · CHCentre for Human Genetics · GBKing's College Hospital · GBKing's College London · GBScripps Research Institute · USUniversity of Montana · US

Funding

Support Component D/Vaccine Discovery, Concept to ClinicUM1AI100663 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI CRISPIN, MAX · 2012 to 2018
$131.5M
Intersubunit crosstalk in the tripartite arenavirus envelope glycoproteinR15AI119803 · NIAID · UNIVERSITY OF MONTANA · PI NUNBERG, JACK H · 2016 to 2016
$427k
Medical Research Council MC_PC_15068Medical Research Council MR/J007897/1Medical Research Council MR/K024426/1Medical Research Council MR/L009528/1Medical Research Council MR/N002091/1NIAID NIH HHS R15 AI119803NIAID NIH HHS UM1 AI100663Wellcome TrustWellcome Trust 203141/Z/16/Z
6 · The paper itself

Abstract

Transmission of hemorrhagic fever New World arenaviruses from their rodent reservoirs to human populations poses substantial public health and economic dangers. These zoonotic events are enabled by the specific interaction between the New World arenaviral attachment glycoprotein, GP1, and cell surface human transferrin receptor (hTfR1). Here, we present the structural basis for how a mouse-derived neutralizing antibody (nAb), OD01, disrupts this interaction by targeting the receptor-binding surface of the GP1 glycoprotein from Junín virus (JUNV), a hemorrhagic fever arenavirus endemic in central Argentina. Comparison of our structure with that of a previously reported nAb complex (JUNV GP1-GD01) reveals largely overlapping epitopes but highly distinct antibody-binding modes. Despite differences in GP1 recognition, we find that both antibodies present a key tyrosine residue, albeit on different chains, that inserts into a central pocket on JUNV GP1 and effectively mimics the contacts made by the host TfR1. These data provide a molecular-level description of how antibodies derived from different germline origins arrive at equivalent immunological solutions to virus neutralization.

Indexed as

Neutralization TestsAntibodies, MonoclonalAntibodies, NeutralizingAntibodies, ViralBinding SitesCrystallography, X-RayEnzyme-Linked Immunosorbent AssayEpitopesGlycoproteinsHEK293 CellsHemorrhagic Fever, AmericanHumansImmune SystemJunin virusProtein BindingRecombinant ProteinsAntibodies, MonoclonalAntibodies, NeutralizingAntibodies, ViralEpitopesGlycoproteinsRecombinant ProteinsViral Envelope Proteinsantibody responsearenavirusglycoproteinhemorrhagic feverstructure

Identifiers

PMID28630325
PMCPMC5502616
OpenAlexW2723385262

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.