Evidence map›Paper›PMID 26775851›Full record

ArticleJournal of immunological methods2016

Optimizing selection of large animals for antibody production by screening immune response to standard vaccines.

Mary K Thompson, Peter C Fridy, Sarah Keegan, Brian T Chait, David Fenyö, Michael P Rout

Open access · greenAbstract read
In one paragraph

Article in Journal of immunological methods, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

6 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Nanobody Repertoires for Exposing Vulnerabilities of SARS-CoV-2.bioRxiv : the preprint server for biology · 2021
    Article
  5. Review
  6. 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

6 authors at 2 institutions in 1 country.

Mary K ThompsonLaboratory of Cellular and Structural Biology, The Rockefeller University, New York, NY, USA.
Peter C FridyLaboratory of Cellular and Structural Biology, The Rockefeller University, New York, NY, USA.
Sarah KeeganCenter for Health Informatics and Bioinformatics, New York University School of Medicine, New York, NY, USA.
Brian T ChaitLaboratory of Mass Spectrometry and Gaseous Ion Chemistry, The Rockefeller University, New York, NY, USA.
David FenyöCenter for Health Informatics and Bioinformatics, New York University School of Medicine, New York, NY, USA.
Michael P RoutLaboratory of Cellular and Structural Biology, The Rockefeller University, New York, NY, USA. Electronic address: rout@rockefeller.edu.
Rockefeller University · USNew York University · US

Funding

TR&D Project 4. The Imaging Stage: Multiscale Spatiotemporal Modeling of Macromolecular Systems in Cellular NeighborhoodsP41GM109824 · NIGMS · ROCKEFELLER UNIVERSITY · PI ROUT, MICHAEL P · 2014 to 2023
$18.8M
National Resource for Mass Spectrom of Biological MacromoleculesP41GM103314 · NIGMS · ROCKEFELLER UNIVERSITY · PI CHAIT, BRIAN T · 2012 to 2017
$9.9M
NIGMS NIH HHS P41 GM103314NIGMS NIH HHS P41 GM109824
6 · The paper itself

Abstract

Antibodies made in large animals are integral to many biomedical research endeavors. Domesticated herd animals like goats, sheep, donkeys, horses and camelids all offer distinct advantages in antibody production. However, their cost of use is often prohibitive, especially where poor antigen response is commonplace; choosing a non-responsive animal can set a research program back or even prevent experiments from moving forward entirely. Over the course of production of antibodies from llamas, we found that some animals consistently produced a higher humoral antibody response than others, even to highly divergent antigens, as well as to their standard vaccines. Based on our initial data, we propose that these "high level responders" could be pre-selected by checking antibody titers against common vaccines given to domestic farm animals. Thus, time and money can be saved by reducing the chances of getting poor responding animals and minimizing the use of superfluous animals.

Indexed as

Antibody FormationAnimalsAntibodies, ViralCamelids, New WorldFemaleGreen Fluorescent ProteinsLuminescent ProteinsMaleRabies VaccinesRabies virusRed Fluorescent ProteinSheepVaccinationAntibodies, ViralGreen Fluorescent ProteinsLuminescent ProteinsRabies VaccinesRed Fluorescent ProteinAntibody generationAntigenCamelid antibodyImmunizationVaccine

Identifiers

PMID26775851
PMCPMC4769958
OpenAlexW2227468295

What OpenQuestion holds

Textmetadata
LicenceTDM
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.