Evidence map›Paper›PMID 35091550›Full record

ArticleNature communications2022

Host receptor-targeted therapeutic approach to counter pathogenic New World mammarenavirus infections.

Brady T Hickerson, Tracy R Daniels-Wells, Cristian Payes, Lars E Clark, Pierre V Candelaria, Kevin W Bailey, Eric J Sefing, Samantha Zink, James Ziegenbein, Jonathan Abraham and 3 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

13 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. A proimmunotoxin nanodrug targeting AIDS-associated non-Hodgkin lymphoma.Journal of controlled release : official journal of the Controlled Release Society · 2026
    Article
  7. Article
  8. Article
  9. Article
  10. Entry inhibitors as arenavirus antivirals.Frontiers in microbiology · 2024
    Review
  11. Article
  12. Article
  13. Review
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

13 authors at 5 institutions in 2 countries.

Brady T Hickerson *Department of Animal, Dairy and Veterinary Sciences, Utah State University, Logan, UT, USA.
Tracy R Daniels-Wells *Division of Surgical Oncology, Department of Surgery, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.ORCID http://orcid.org/0000-0002-8277-9702
Cristian PayesInstituto de Biología y Medicina Experimental (IBYME CONICET), Buenos Aires, Argentina.
Lars E ClarkDepartment of Microbiology, Blavatnik Institute, Harvard Medical School, Boston, MA, USA.ORCID http://orcid.org/0000-0002-6093-7597
Pierre V CandelariaDivision of Surgical Oncology, Department of Surgery, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.
Kevin W BaileyDepartment of Animal, Dairy and Veterinary Sciences, Utah State University, Logan, UT, USA.
Eric J SefingDepartment of Animal, Dairy and Veterinary Sciences, Utah State University, Logan, UT, USA.
Samantha ZinkDepartment of Chemistry and Biochemistry, University of California, Los Angeles (UCLA), Los Angeles, CA, USA.ORCID http://orcid.org/0000-0002-3220-8290
James ZiegenbeinDepartment of Chemistry and Biochemistry, University of California, Los Angeles (UCLA), Los Angeles, CA, USA.
Jonathan AbrahamDepartment of Microbiology, Blavatnik Institute, Harvard Medical School, Boston, MA, USA.ORCID http://orcid.org/0000-0002-7937-3920
Gustavo HelgueraInstituto de Biología y Medicina Experimental (IBYME CONICET), Buenos Aires, Argentina. gustavoh@ibyme.conicet.gov.ar.ORCID http://orcid.org/0000-0003-1509-3564
Manuel L PenichetDivision of Surgical Oncology, Department of Surgery, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA. penichet@mednet.ucla.edu.
Brian B GowenDepartment of Animal, Dairy and Veterinary Sciences, Utah State University, Logan, UT, USA. brian.gowen@usu.edu.ORCID http://orcid.org/0000-0001-9113-2575
University of California, Los Angeles · USUtah State University · USBrigham and Women's Hospital · USConsejo Nacional de Investigaciones Científicas y Técnicas · ARHarvard University · US

Funding

User Training and OutreachP30GM124165 · NIGMS · CORNELL UNIVERSITY · PI Nozomi Ando, J Christopher Fromme · 2018 to 2026
$34.2M
Overall EvaluationP41GM103403 · NIGMS · CORNELL UNIVERSITY · PI EALICK, STEVEN E · 2012 to 2017
$14.3M
A Novel Strategy Targeting TfR1 for the Prevention/Treatment of AIDS-related NHLR01CA196266 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI MARTINEZ-MAZA, OTONIEL, PENICHET, MANUEL L · 2016 to 2020
$3.4M
Pixel Array Detector for Macromolecular CrystallographyS10OD021527 · OD · CORNELL UNIVERSITY · PI EALICK, STEVEN E · 2016 to 2016
$2.0M
Development of a broad spectrum therapeutic against New World hemorrhagic feversR21AI135851 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI RODRIGUEZ, JOSE ALFONSO · 2018 to 2019
$429k
NCI NIH HHS R01 CA196266NIAID NIH HHS R21 AI135851NIGMS NIH HHS P30 GM124165NIGMS NIH HHS P41 GM103403NIH HHS S10 OD021527
6 · The paper itself

Abstract

Five New World mammarenaviruses (NWMs) cause life-threatening hemorrhagic fever (HF). Cellular entry by these viruses is mediated by human transferrin receptor 1 (hTfR1). Here, we demonstrate that an antibody (ch128.1/IgG1) which binds the apical domain of hTfR1, potently inhibits infection of attenuated and pathogenic NWMs in vitro. Computational docking of the antibody Fab crystal structure onto the known structure of hTfR1 shows an overlapping receptor-binding region shared by the Fab and the viral envelope glycoprotein GP1 subunit that binds hTfR1, and we demonstrate competitive inhibition of NWM GP1 binding by ch128.1/IgG1 as the principal mechanism of action. Importantly, ch128.1/IgG1 protects hTfR1-expressing transgenic mice against lethal NWM challenge. Additionally, the antibody is well-tolerated and only partially reduces ferritin uptake. Our findings provide the basis for the development of a novel, host receptor-targeted antibody therapeutic broadly applicable to the treatment of HF of NWM etiology.

Indexed as

A549 CellsAnimalsAntibodies, MonoclonalAntigens, CDArenaviridaeChlorocebus aethiopsHemorrhagic Fever, AmericanHost-Pathogen InteractionsHumansJunin virusMiceMice, Inbred C57BLMice, TransgenicMolecular Docking SimulationProtein BindingReceptors, TransferrinAntibodies, MonoclonalAntigens, CDCD71 antigenReceptors, TransferrinViral Envelope Proteins

Identifiers

PMID35091550
PMCPMC8799657
OpenAlexW4210753758

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.