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


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2020
Historique:
received: 03 04 2020
accepted: 15 06 2020
entrez: 26 6 2020
pubmed: 26 6 2020
medline: 9 9 2020
Statut: epublish

Résumé

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.

Identifiants

pubmed: 32584899
doi: 10.1371/journal.pone.0235422
pii: PONE-D-20-09236
pmc: PMC7316291
doi:

Substances chimiques

Histocompatibility Antigens Class II 0
Interleukin-6 0
Liposomes 0
Respiratory System Agents 0
Toll-Like Receptor 3 0
Toll-Like Receptor 9 0
Nitric Oxide 31C4KY9ESH
Interferon-gamma 82115-62-6

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0235422

Subventions

Organisme : NIH HHS
ID : T35 OD015130
Pays : United States

Déclaration de conflit d'intérêts

SD, AC and RH hold stock options and corporate positions at LaPorte Ag Therapeutics, Inc, a Colorado State University-based startup company developing the LTC immunotherapy platform technology. WW, LC and SD are patent holders for the LTC technology. The issued US patent covering this technology is US 10,512, 687, issued Dec 24, 2019. Any commercial affiliation of the above-mentioned authors with LaPorte Ag Therapeutics, Elanco Inc. or Hunter Cattle Co. did not play a role in the study design, data interpretation, or publication decisions. Accordingly, this does not alter our adherence to PLOS ONE policies and sharing data and materials.

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Auteurs

William Wheat (W)

Department 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.

Lyndah Chow (L)

Department 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 Rozo (V)

Department 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 Herman (J)

Department 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.

Kelly Still Brooks (K)

Department 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 Colbath (A)

Department 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 Hunter (R)

Hunter Cattle Company, Wheatland, Wyoming, United States of America.

Steven Dow (S)

Department 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.

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Classifications MeSH