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Local immune and microbiological responses to mucosal administration of a Liposome-TLR agonist immunotherapeutic in dogs
BACKGROUND: Non-specific immunotherapeutics have been evaluated previously in dogs, primarily for cancer treatment. However, there remains a need for a more broadly targeted, general purpose immunotherapeutic capable of activating innate immune defenses for non-specific protection or early treatment...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6743184/ https://www.ncbi.nlm.nih.gov/pubmed/31519215 http://dx.doi.org/10.1186/s12917-019-2073-8 |
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author | Wheat, William Chow, Lyndah Kuzmik, Alana Soontararak, Sirikul Kurihara, Jade Lappin, Michael Dow, Steven |
author_facet | Wheat, William Chow, Lyndah Kuzmik, Alana Soontararak, Sirikul Kurihara, Jade Lappin, Michael Dow, Steven |
author_sort | Wheat, William |
collection | PubMed |
description | BACKGROUND: Non-specific immunotherapeutics have been evaluated previously in dogs, primarily for cancer treatment. However, there remains a need for a more broadly targeted, general purpose immunotherapeutic capable of activating innate immune defenses for non-specific protection or early treatment of viral and bacterial infections. To address need, our group has developed a liposomal immune stimulant (liposome-TLR complexes, LTC) containing TLR 3 and 9 agonists specifically designed to activate mucosal immune defenses in sites such as nasal cavity and oropharynx, following topical delivery. In this study, we evaluated the local immune stimulatory properties of LTC in vitro and in healthy purpose-bred dogs, including activation of cellular recruitment and cytokine production. The ability of LTC treatment to elicit effective antiviral immunity was assessed in dogs following a canine herpesvirus outbreak, and the impact of LTC treatment on the local microbiome of the oropharynx was also investigated. RESULTS: These studies revealed that LTC potently activated innate immune responses in vitro and triggered significant recruitment of inflammatory monocytes and T cells into the nasal cavity and oropharynx of healthy dogs. Administration of LTC to dogs shortly after an outbreak of canine herpesvirus infection resulted in significant reduction in clinical signs of infection. Interestingly, administration of LTC to healthy dogs did not disrupt the microbiome in the oropharynx, suggesting resiliency of the microflora to transient immune activation. CONCLUSIONS: Taken together, these results indicate that LTC administration mucosally to dogs can trigger local innate immune activation and activation of antiviral immunity, without significantly disrupting the composition of the local microbiome. Thus, the LTC immune stimulant has potential for use as a non-specific immunotherapy for prevention or early treatment of viral and bacterial infections in dogs. |
format | Online Article Text |
id | pubmed-6743184 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-67431842019-09-16 Local immune and microbiological responses to mucosal administration of a Liposome-TLR agonist immunotherapeutic in dogs Wheat, William Chow, Lyndah Kuzmik, Alana Soontararak, Sirikul Kurihara, Jade Lappin, Michael Dow, Steven BMC Vet Res Research Article BACKGROUND: Non-specific immunotherapeutics have been evaluated previously in dogs, primarily for cancer treatment. However, there remains a need for a more broadly targeted, general purpose immunotherapeutic capable of activating innate immune defenses for non-specific protection or early treatment of viral and bacterial infections. To address need, our group has developed a liposomal immune stimulant (liposome-TLR complexes, LTC) containing TLR 3 and 9 agonists specifically designed to activate mucosal immune defenses in sites such as nasal cavity and oropharynx, following topical delivery. In this study, we evaluated the local immune stimulatory properties of LTC in vitro and in healthy purpose-bred dogs, including activation of cellular recruitment and cytokine production. The ability of LTC treatment to elicit effective antiviral immunity was assessed in dogs following a canine herpesvirus outbreak, and the impact of LTC treatment on the local microbiome of the oropharynx was also investigated. RESULTS: These studies revealed that LTC potently activated innate immune responses in vitro and triggered significant recruitment of inflammatory monocytes and T cells into the nasal cavity and oropharynx of healthy dogs. Administration of LTC to dogs shortly after an outbreak of canine herpesvirus infection resulted in significant reduction in clinical signs of infection. Interestingly, administration of LTC to healthy dogs did not disrupt the microbiome in the oropharynx, suggesting resiliency of the microflora to transient immune activation. CONCLUSIONS: Taken together, these results indicate that LTC administration mucosally to dogs can trigger local innate immune activation and activation of antiviral immunity, without significantly disrupting the composition of the local microbiome. Thus, the LTC immune stimulant has potential for use as a non-specific immunotherapy for prevention or early treatment of viral and bacterial infections in dogs. BioMed Central 2019-09-13 /pmc/articles/PMC6743184/ /pubmed/31519215 http://dx.doi.org/10.1186/s12917-019-2073-8 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Wheat, William Chow, Lyndah Kuzmik, Alana Soontararak, Sirikul Kurihara, Jade Lappin, Michael Dow, Steven Local immune and microbiological responses to mucosal administration of a Liposome-TLR agonist immunotherapeutic in dogs |
title | Local immune and microbiological responses to mucosal administration of a Liposome-TLR agonist immunotherapeutic in dogs |
title_full | Local immune and microbiological responses to mucosal administration of a Liposome-TLR agonist immunotherapeutic in dogs |
title_fullStr | Local immune and microbiological responses to mucosal administration of a Liposome-TLR agonist immunotherapeutic in dogs |
title_full_unstemmed | Local immune and microbiological responses to mucosal administration of a Liposome-TLR agonist immunotherapeutic in dogs |
title_short | Local immune and microbiological responses to mucosal administration of a Liposome-TLR agonist immunotherapeutic in dogs |
title_sort | local immune and microbiological responses to mucosal administration of a liposome-tlr agonist immunotherapeutic in dogs |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6743184/ https://www.ncbi.nlm.nih.gov/pubmed/31519215 http://dx.doi.org/10.1186/s12917-019-2073-8 |
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