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Naturally derived cytokine peptides limit virus replication and severe disease during influenza A virus infection

OBJECTIVES: Novel host‐targeted therapeutics could treat severe influenza A virus (IAV) infections, with reduced risk of drug resistance. LAT8881 is a synthetic form of the naturally occurring C‐terminal fragment of human growth hormone. Acting independently of the growth hormone receptor, it can re...

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Autores principales: Harpur, Christopher M, West, Alison C, Le Page, Mélanie A, Lam, Maggie, Hodges, Christopher, Oseghale, Osezua, Gearing, Andrew J, Tate, Michelle D
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10034483/
https://www.ncbi.nlm.nih.gov/pubmed/36969366
http://dx.doi.org/10.1002/cti2.1443
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author Harpur, Christopher M
West, Alison C
Le Page, Mélanie A
Lam, Maggie
Hodges, Christopher
Oseghale, Osezua
Gearing, Andrew J
Tate, Michelle D
author_facet Harpur, Christopher M
West, Alison C
Le Page, Mélanie A
Lam, Maggie
Hodges, Christopher
Oseghale, Osezua
Gearing, Andrew J
Tate, Michelle D
author_sort Harpur, Christopher M
collection PubMed
description OBJECTIVES: Novel host‐targeted therapeutics could treat severe influenza A virus (IAV) infections, with reduced risk of drug resistance. LAT8881 is a synthetic form of the naturally occurring C‐terminal fragment of human growth hormone. Acting independently of the growth hormone receptor, it can reduce inflammation‐induced damage and promote tissue repair in an animal model of osteoarthritis. LAT8881 has been assessed in clinical trials for the treatment of obesity and neuropathy and has an excellent safety profile. We investigated the potential for LAT8881, its metabolite LAT9991F and LAT7771 derived from prolactin, a growth hormone structural homologue, to treat severe IAV infection. METHODS: LAT8881, LAT9991F and LAT7771 were evaluated for their effects on cell viability and IAV replication in vitro, as well as their potential to limit disease in a preclinical mouse model of severe IAV infection. RESULTS: In vitro LAT8881 treatment enhanced cell viability, particularly in the presence of cytotoxic stress, which was countered by siRNA inhibition of host lanthionine synthetase C‐like proteins. Daily intranasal treatment of mice with LAT8881 or LAT9991F, but not LAT7771, from day 1 postinfection significantly improved influenza disease resistance, which was associated with reduced infectious viral loads, reduced pro‐inflammatory cytokines and increased abundance of protective alveolar macrophages. LAT8881 treatment in combination with the antiviral oseltamivir phosphate led to more pronounced reduction in markers of disease severity than treatment with either compound alone. CONCLUSION: These studies provide the first evidence identifying LAT8881 and LAT9991F as novel host‐protective therapies that improve survival, limit viral replication, reduce local inflammation and curtail tissue damage during severe IAV infection. Evaluation of LAT8881 and LAT9991F in other infectious and inflammatory conditions of the airways is warranted.
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spelling pubmed-100344832023-03-24 Naturally derived cytokine peptides limit virus replication and severe disease during influenza A virus infection Harpur, Christopher M West, Alison C Le Page, Mélanie A Lam, Maggie Hodges, Christopher Oseghale, Osezua Gearing, Andrew J Tate, Michelle D Clin Transl Immunology Original Articles OBJECTIVES: Novel host‐targeted therapeutics could treat severe influenza A virus (IAV) infections, with reduced risk of drug resistance. LAT8881 is a synthetic form of the naturally occurring C‐terminal fragment of human growth hormone. Acting independently of the growth hormone receptor, it can reduce inflammation‐induced damage and promote tissue repair in an animal model of osteoarthritis. LAT8881 has been assessed in clinical trials for the treatment of obesity and neuropathy and has an excellent safety profile. We investigated the potential for LAT8881, its metabolite LAT9991F and LAT7771 derived from prolactin, a growth hormone structural homologue, to treat severe IAV infection. METHODS: LAT8881, LAT9991F and LAT7771 were evaluated for their effects on cell viability and IAV replication in vitro, as well as their potential to limit disease in a preclinical mouse model of severe IAV infection. RESULTS: In vitro LAT8881 treatment enhanced cell viability, particularly in the presence of cytotoxic stress, which was countered by siRNA inhibition of host lanthionine synthetase C‐like proteins. Daily intranasal treatment of mice with LAT8881 or LAT9991F, but not LAT7771, from day 1 postinfection significantly improved influenza disease resistance, which was associated with reduced infectious viral loads, reduced pro‐inflammatory cytokines and increased abundance of protective alveolar macrophages. LAT8881 treatment in combination with the antiviral oseltamivir phosphate led to more pronounced reduction in markers of disease severity than treatment with either compound alone. CONCLUSION: These studies provide the first evidence identifying LAT8881 and LAT9991F as novel host‐protective therapies that improve survival, limit viral replication, reduce local inflammation and curtail tissue damage during severe IAV infection. Evaluation of LAT8881 and LAT9991F in other infectious and inflammatory conditions of the airways is warranted. John Wiley and Sons Inc. 2023-03-23 /pmc/articles/PMC10034483/ /pubmed/36969366 http://dx.doi.org/10.1002/cti2.1443 Text en © 2023 The Authors. Clinical & Translational Immunology published by John Wiley & Sons Australia, Ltd on behalf of Australian and New Zealand Society for Immunology, Inc. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Harpur, Christopher M
West, Alison C
Le Page, Mélanie A
Lam, Maggie
Hodges, Christopher
Oseghale, Osezua
Gearing, Andrew J
Tate, Michelle D
Naturally derived cytokine peptides limit virus replication and severe disease during influenza A virus infection
title Naturally derived cytokine peptides limit virus replication and severe disease during influenza A virus infection
title_full Naturally derived cytokine peptides limit virus replication and severe disease during influenza A virus infection
title_fullStr Naturally derived cytokine peptides limit virus replication and severe disease during influenza A virus infection
title_full_unstemmed Naturally derived cytokine peptides limit virus replication and severe disease during influenza A virus infection
title_short Naturally derived cytokine peptides limit virus replication and severe disease during influenza A virus infection
title_sort naturally derived cytokine peptides limit virus replication and severe disease during influenza a virus infection
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10034483/
https://www.ncbi.nlm.nih.gov/pubmed/36969366
http://dx.doi.org/10.1002/cti2.1443
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