Evidence map›Paper›PMID 32508764›Full record

ArticleFrontiers in microbiology2020

Anti-HFRS Human IgG Produced in Transchromosomic Bovines Has Potent Hantavirus Neutralizing Activity and Is Protective in Animal Models.

Casey C Perley, Rebecca L Brocato, Hua Wu, Christoph Bausch, Priya P Karmali, Jerel B Vega, Melanie V Cohen, Brandon Somerville, Steven A Kwilas, Lucia M Principe and 4 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in microbiology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
0.6field-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

19 citing papers in PubMed, 28 citations in OpenAlex.

  1. Trial
  2. Generation and Characterization of the Human Anti-HTNV Antibody KJJ4.International journal of molecular sciences · 2026
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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

14 authors at 3 institutions in 1 country.

Casey C PerleyVirology Division, United States Army Medical Research Institute of Infectious Diseases, Frederick, MD, United States.
Rebecca L BrocatoVirology Division, United States Army Medical Research Institute of Infectious Diseases, Frederick, MD, United States.
Hua WuSAB Biotherapeutics Inc., Sioux Falls, SD, United States.
Christoph BauschSAB Biotherapeutics Inc., Sioux Falls, SD, United States.
Priya P KarmaliArcturus Therapeutics Inc., San Diego, CA, United States.
Jerel B VegaArcturus Therapeutics Inc., San Diego, CA, United States.
Melanie V CohenVirology Division, United States Army Medical Research Institute of Infectious Diseases, Frederick, MD, United States.
Brandon SomervilleVirology Division, United States Army Medical Research Institute of Infectious Diseases, Frederick, MD, United States.
Steven A KwilasVirology Division, United States Army Medical Research Institute of Infectious Diseases, Frederick, MD, United States.
Lucia M PrincipeVirology Division, United States Army Medical Research Institute of Infectious Diseases, Frederick, MD, United States.
Joshua ShamblinVirology Division, United States Army Medical Research Institute of Infectious Diseases, Frederick, MD, United States.
Padmanabh ChivukulaArcturus Therapeutics Inc., San Diego, CA, United States.
Eddie SullivanSAB Biotherapeutics Inc., Sioux Falls, SD, United States.
Jay W HooperVirology Division, United States Army Medical Research Institute of Infectious Diseases, Frederick, MD, United States.
United States Army Medical Research Institute of Infectious Diseases · USArcturus Therapeutics (United States) · USSab Biotherapeutics (United States) · US

Funding

Advancing a Candidate Polyclonal Antibody Therapy for Hantavirus DiseaseR01AI132313 · NIAID · GENEVA FOUNDATION · PI HOOPER, JAY WILLIAMS · 2017 to 2021
$4.6M
NIAID NIH HHS R01 AI132313
6 · The paper itself

Abstract

We explored an emerging technology to produce anti-Hantaan virus (HTNV) and anti-Puumala virus (PUUV) neutralizing antibodies for use as pre- or post-exposure prophylactics. The technology involves hyperimmunization of transchomosomic bovines (TcB) engineered to express human polyclonal IgG antibodies with HTNV and PUUV DNA vaccines encoding G

Indexed as

hamsterhantaanhantavirusHFRSmarmosetpassive transferpuumalatranschromosomic bovine

Identifiers

PMID32508764
PMCPMC7252588
OpenAlexW3023003688

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.