Evidence map›Paper›PMID 31900422›Full record

ArticleNature communications2020

Rational design of universal immunotherapy for TfR1-tropic arenaviruses.

Hadas Cohen-Dvashi, Ron Amon, Krystle N Agans, Robert W Cross, Aliza Borenstein-Katz, Mathieu Mateo, Sylvain Baize, Vered Padler-Karavani, Thomas W Geisbert, Ron Diskin

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
0.4field-weighted citation impact, top 25% 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

16 citing papers in PubMed, 25 citations in OpenAlex.

  1. Review
  2. Article
  3. Enhanced screening via a pure DNA-encoded peptide library enabled by an Fmoc modification.Proceedings of the National Academy of Sciences of the United States of America · 2026
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  7. Entry inhibitors as arenavirus antivirals.Frontiers in microbiology · 2024
    Review
  8. Lassa Virus Countermeasures.Current topics in microbiology and immunology · 2023
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. 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

10 authors at 4 institutions in 3 countries.

Hadas Cohen-DvashiDepartment of Structural Biology, Weizmann Institute of Science, Rehovot, 7610001, Israel.
Ron AmonDepartment of Cell Research and Immunology, Tel Aviv University, Tel Aviv, 69978, Israel.
Krystle N AgansGalveston National Laboratory, University of Texas Medical Branch, Galveston, TX, 77555, USA.ORCID http://orcid.org/0000-0002-7319-6935
Robert W CrossGalveston National Laboratory, University of Texas Medical Branch, Galveston, TX, 77555, USA.
Aliza Borenstein-KatzDepartment of Structural Biology, Weizmann Institute of Science, Rehovot, 7610001, Israel.
Mathieu MateoUnité de Biologie des Infections Virales Emergentes, Institut Pasteur, Centre International de Recherche en Infectiologie (INSERM, CNRS, ENS Lyon, Université Lyon I), Lyon, France.ORCID http://orcid.org/0000-0001-7941-0245
Sylvain BaizeUnité de Biologie des Infections Virales Emergentes, Institut Pasteur, Centre International de Recherche en Infectiologie (INSERM, CNRS, ENS Lyon, Université Lyon I), Lyon, France.
Vered Padler-KaravaniDepartment of Cell Research and Immunology, Tel Aviv University, Tel Aviv, 69978, Israel.
Thomas W GeisbertGalveston National Laboratory, University of Texas Medical Branch, Galveston, TX, 77555, USA.
Ron DiskinDepartment of Structural Biology, Weizmann Institute of Science, Rehovot, 7610001, Israel. ron.diskin@weizmann.ac.il.ORCID http://orcid.org/0000-0002-2837-5897
The University of Texas Medical Branch at Galveston · USWeizmann Institute of Science · ILTel Aviv University · ILUniversité Claude Bernard Lyon 1 · FR

Funding

Regulatory Compliance Core - Galveston National Laboratory BSL4 OperationsUC7AI094660 · NIAID · UNIVERSITY OF TEXAS MED BR GALVESTON · PI Gene Garrard Olinger · 2011 to 2026
$208.8M
NIAID NIH HHS UC7 AI094660
6 · The paper itself

Abstract

Certain arenaviruses that circulate in rodent populations can cause life-threatening hemorrhagic fevers when they infect humans. Due to their efficient transmission, arenaviruses pose a severe risk for outbreaks and might be exploited as biological weapons. Effective countermeasures against these viruses are highly desired. Ideally, a single remedy would be effective against many or even all the pathogenic viruses in this family. However, despite the fact that all pathogenic arenaviruses from South America utilize transferrin receptor 1 (TfR1) as a cellular receptor, their viral glycoproteins are highly diversified, impeding efforts to isolate cross-neutralizing antibodies. Here we address this problem using a rational design approach to target TfR1-tropic arenaviruses with high potency and breadth. The pan-reactive molecule is highly effective against all arenaviruses that were tested, offering a universal therapeutic approach. Our design scheme avoids the shortcomings of previous immunoadhesins and can be used to combat other zoonotic pathogens.

Indexed as

ImmunotherapyAntibodies, NeutralizingAntibodies, ViralArenaviridae InfectionsArenavirusDrug DesignHumansReceptors, TransferrinReceptors, VirusViral ProteinsAntibodies, NeutralizingAntibodies, ViralReceptors, TransferrinReceptors, VirusViral Proteins

Identifiers

PMID31900422
PMCPMC6941993
OpenAlexW2998020628

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.