Evidence map›Paper›PMID 32584899›Full record

ArticlePloS one2020

Non-specific protection from respiratory tract infections in cattle generated by intranasal administration of an innate immune stimulant.

William Wheat, Lyndah Chow, Vanessa Rozo, Julia Herman, Kelly Still Brooks, Aimee Colbath, Randy Hunter, Steven Dow

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2020. 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
1.3field-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

13 citing papers in PubMed, 19 citations in OpenAlex.

  1. Phagocytosis ofInternational 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

8 authors at 1 institution in 1 country.

William WheatDepartment of Clinical Sciences, From the Center for Immune and Regenerative Medicine, College of Veterinary Medicine and Biomedical Sciences, Colorado State University, Ft. Collins, Colorado, United States of America.ORCID 0000-0003-4229-3617
Lyndah ChowDepartment of Clinical Sciences, From the Center for Immune and Regenerative Medicine, College of Veterinary Medicine and Biomedical Sciences, Colorado State University, Ft. Collins, Colorado, United States of America.
Vanessa RozoDepartment of Clinical Sciences, From the Center for Immune and Regenerative Medicine, College of Veterinary Medicine and Biomedical Sciences, Colorado State University, Ft. Collins, Colorado, United States of America.
Julia HermanDepartment of Clinical Sciences, From the Center for Immune and Regenerative Medicine, College of Veterinary Medicine and Biomedical Sciences, Colorado State University, Ft. Collins, Colorado, United States of America.ORCID 0000-0002-7766-4337
Kelly Still BrooksDepartment of Clinical Sciences, From the Center for Immune and Regenerative Medicine, College of Veterinary Medicine and Biomedical Sciences, Colorado State University, Ft. Collins, Colorado, United States of America.
Aimee ColbathDepartment of Clinical Sciences, From the Center for Immune and Regenerative Medicine, College of Veterinary Medicine and Biomedical Sciences, Colorado State University, Ft. Collins, Colorado, United States of America.
Randy HunterHunter Cattle Company, Wheatland, Wyoming, United States of America.
Steven DowDepartment of Clinical Sciences, From the Center for Immune and Regenerative Medicine, College of Veterinary Medicine and Biomedical Sciences, Colorado State University, Ft. Collins, Colorado, United States of America.
Colorado State University · US

Funding

Veterinary Scholars Summer Research ProgramT35OD015130 · OD · COLORADO STATE UNIVERSITY · PI ZABEL, MARK D · 2012 to 2021
$654k
NIH HHS T35 OD015130
6 · The paper itself

Abstract

Alternatives to antibiotics for prevention of respiratory tract infections in cattle are urgently needed given the increasing public and regulatory pressure to reduce overall antibiotic usage. Activation of local innate immune defenses in the upper respiratory tract is one strategy to induce non-specific protection against infection with the diverse array of viral and bacterial pathogens associated with bovine respiratory disease complex (BRDC), while avoiding the use of antibiotics. Our prior studies in rodent models demonstrated that intranasal administration of liposome-TLR complexes (LTC) as a non-specific immune stimulant generated high levels of protection against lethal bacterial and viral pathogens. Therefore, we conducted studies to assess LTC induction of local immune responses and protective immunity to BRDC in cattle. In vitro, LTC were shown to activate peripheral blood mononuclear cells in cattle, which was associated with secretion of INFγ and IL-6. Macrophage activation with LTC triggered intracellular killing of Mannheimia hemolytica and several other bacterial pathogens. In studies in cattle, intranasal administration of LTC demonstrated dose-dependent activation of local innate immune responses in the nasopharynx, including recruitment of monocytes and prolonged upregulation (at least 2 weeks) of innate immune cytokine gene expression by nasopharyngeal mucosal cells. In a BRDC challenge study, intranasal administration of LTC prior to pathogen exposure resulted in significant reduction in both clinical signs of infection and disease-associated euthanasia rates. These findings indicate that intranasal administration of a non-specific innate immune stimulant can be an effective method of rapidly generating generalized protection from mixed viral and bacterial respiratory tract infections in cattle.

Indexed as

Administration, IntranasalAnimalsBovine Respiratory Disease ComplexCattleHistocompatibility Antigens Class IIImmunity, InnateInterferon-gammaInterleukin-6Leukocytes, MononuclearLiposomesMacrophagesMannheimia haemolyticaNasopharynxNitric OxidePhagocytosisRespiratory System AgentsHistocompatibility Antigens Class IIInterferon-gammaInterleukin-6LiposomesNitric OxideRespiratory System AgentsToll-Like Receptor 3Toll-Like Receptor 9

Identifiers

PMID32584899
PMCPMC7316291
OpenAlexW3037889955

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.