Evidence map›Paper›PMID 37736038›Full record

ArticleiScience2023

Transchromosomic bovine-derived anti-SARS-CoV-2 polyclonal human antibodies protects hACE2 transgenic hamsters against multiple variants.

Theron Gilliland, Matthew Dunn, Yanan Liu, Maria D H Alcorn, Yutaka Terada, Shauna Vasilatos, Jeneveve Lundy, Rong Li, Sham Nambulli, Deanna Larson and 8 more

Open access · goldAbstract read
In one paragraph

Article in iScience, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

8 citing papers in PubMed, 7 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

18 authors at 3 institutions in 1 country.

Theron GillilandCenter for Vaccine Research and Department of Immunology, University of Pittsburgh, Pittsburgh, PA 15261, USA.
Matthew DunnCenter for Vaccine Research and Department of Immunology, University of Pittsburgh, Pittsburgh, PA 15261, USA.
Yanan LiuDepartment of Animal Dairy, Veterinary Sciences, Utah State University, Logan, UT 84341, USA.
Maria D H AlcornCenter for Vaccine Research and Department of Immunology, University of Pittsburgh, Pittsburgh, PA 15261, USA.
Yutaka TeradaCenter for Vaccine Research and Department of Immunology, University of Pittsburgh, Pittsburgh, PA 15261, USA.
Shauna VasilatosCenter for Vaccine Research and Department of Immunology, University of Pittsburgh, Pittsburgh, PA 15261, USA.
Jeneveve LundyCenter for Vaccine Research and Department of Immunology, University of Pittsburgh, Pittsburgh, PA 15261, USA.
Rong LiDepartment of Animal Dairy, Veterinary Sciences, Utah State University, Logan, UT 84341, USA.
Sham NambulliCenter for Vaccine Research and Department of Microbiology and Molecular Genetics, University of Pittsburgh, Pittsburgh, PA 15261, USA.
Deanna LarsonDepartment of Animal Dairy, Veterinary Sciences, Utah State University, Logan, UT 84341, USA.
Paul DuprexCenter for Vaccine Research and Department of Microbiology and Molecular Genetics, University of Pittsburgh, Pittsburgh, PA 15261, USA.
Hua WuSAb Biotherapeutics, Inc, Sioux Falls, SD 57104, USA.
Thomas LukeSAb Biotherapeutics, Inc, Sioux Falls, SD 57104, USA.
Christoph BauschSAb Biotherapeutics, Inc, Sioux Falls, SD 57104, USA.
Kristi EglandSAb Biotherapeutics, Inc, Sioux Falls, SD 57104, USA.
Eddie SullivanSAb Biotherapeutics, Inc, Sioux Falls, SD 57104, USA.
Zhongde WangDepartment of Animal Dairy, Veterinary Sciences, Utah State University, Logan, UT 84341, USA.
William B KlimstraCenter for Vaccine Research and Department of Immunology, University of Pittsburgh, Pittsburgh, PA 15261, USA.
University of Pittsburgh · USSab Biotherapeutics (United States) · USUtah State University · US

Funding

Practices CoreUC7AI180311 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI William Paul Duprex · 2023 to 2026
$13.2M
NIAID NIH HHS UC7 AI180311
6 · The paper itself

Abstract

Pandemic SARS-CoV-2 has undergone rapid evolution resulting in the emergence of many variants with mutations in the spike protein, some of which appear to evade antibody neutralization, transmit more efficiently, and/or exhibit altered virulence. This raises significant concerns regarding the efficacy of anti-S monoclonal antibody-based therapeutics which have failed against variant SARS-CoV-2 viruses. To address this concern, SAB-185, a human anti-SARS-CoV-2 polyclonal antibody was generated in the DiversitAb platform. SAB-185 exhibited equivalent, robust

Indexed as

Immune responseImmunologyVirology

Identifiers

PMID37736038
PMCPMC10509298
OpenAlexW4386257793

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.