Evidence map›Paper›PMID 28107431›Full record

ArticlePloS one2017

Characterization of a Broadly Reactive Anti-CD40 Agonistic Monoclonal Antibody for Potential Use as an Adjuvant.

Cameron Martin, Suryakant D Waghela, Shehnaz Lokhandwala, Andy Ambrus, Jocelyn Bray, Christina Vuong, Vanitha Vinodkumar, Paul J Dominowski, Sharath Rai, Duncan Mwangi and 2 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.4field-weighted citation impact, top 40% 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

1 citing paper in PubMed, 5 citations in OpenAlex.

  1. 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

12 authors at 2 institutions in 1 country.

Cameron MartinDepartment of Veterinary Pathobiology, Texas A&M University, College Station, Texas, United States of America.ORCID http://orcid.org/0000-0003-0824-3106
Suryakant D WaghelaDepartment of Veterinary Pathobiology, Texas A&M University, College Station, Texas, United States of America.
Shehnaz LokhandwalaDepartment of Veterinary Pathobiology, Texas A&M University, College Station, Texas, United States of America.
Andy AmbrusDepartment of Veterinary Pathobiology, Texas A&M University, College Station, Texas, United States of America.
Jocelyn BrayDepartment of Veterinary Pathobiology, Texas A&M University, College Station, Texas, United States of America.
Christina VuongDepartment of Veterinary Pathobiology, Texas A&M University, College Station, Texas, United States of America.
Vanitha VinodkumarDepartment of Veterinary Pathobiology, Texas A&M University, College Station, Texas, United States of America.
Paul J DominowskiZoetis, Kalamazoo, Michigan, United States of America.
Sharath RaiZoetis, Kalamazoo, Michigan, United States of America.
Duncan MwangiZoetis, Kalamazoo, Michigan, United States of America.
Dennis L FossZoetis, Kalamazoo, Michigan, United States of America.
Waithaka MwangiDepartment of Veterinary Pathobiology, Texas A&M University, College Station, Texas, United States of America.
Texas A&M University · USZoetis (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lack of safe and effective adjuvants is a major hindrance to the development of efficacious vaccines. Signaling via CD40 pathway leads to enhanced antigen processing and presentation, nitric oxide expression, pro-inflammatory cytokine expression by antigen presenting cells, and stimulation of B-cells to undergo somatic hypermutation, immunoglobulin class switching, and proliferation. Agonistic anti-CD40 antibodies have shown promising adjuvant qualities in human and mouse vaccine studies. An anti-CD40 monoclonal antibody (mAb), designated 2E4E4, was identified and shown to have strong agonistic effects on primary cells from multiple livestock species. The mAb recognize swine, bovine, caprine, and ovine CD40, and evoked 25-fold or greater proliferation of peripheral blood mononuclear cells (PBMCs) from these species relative to cells incubated with an isotype control (p<0.001). In addition, the mAb induced significant nitric oxide (p<0.0001) release by bovine macrophages. Furthermore, the mAb upregulated the expression of MHC-II by PBMCs, and stimulated significant (p<0.0001) IL-1α, IL6, IL-8, and TNF-α expression by PBMCs. These results suggest that the mAb 2E4E4 can target and stimulate cells from multiple livestock species and thus, it is a potential candidate for adjuvant development. This is the first study to report an anti-swine CD40 agonistic mAb that is also broadly reactive against multiple species.

Indexed as

Adjuvants, ImmunologicAnimalsAntibodies, MonoclonalCattleCD40 AntigensCross ReactionsCytokinesFemaleFlow CytometryGenes, MHC Class IIGoatsHEK293 CellsHumansLeukocytes, MononuclearMiceMice, Inbred BALB CAdjuvants, ImmunologicAntibodies, MonoclonalCD40 AntigensCytokines

Identifiers

PMID28107431
PMCPMC5249191
OpenAlexW2578129318

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.