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Oral Supplementation with AHCC(®), a Standardized Extract of Cultured Lentinula edodes Mycelia, Enhances Host Resistance against SARS-CoV-2 Infection

The coronavirus disease 2019 (COVID-19) pandemic has significantly impacted global public health safety and the economy. Multiple antiviral drugs have been developed, and some have received regulatory approval and/or authorization. The use of nutraceuticals can be beneficial for preventing and treat...

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Autores principales: Singh, Ankita, Adam, Awadalkareem, Rodriguez, Leslie, Peng, Bi-Hung, Wang, Binbin, Xie, Xuping, Shi, Pei-Yong, Homma, Kohei, Wang, Tian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10144296/
https://www.ncbi.nlm.nih.gov/pubmed/37111440
http://dx.doi.org/10.3390/pathogens12040554
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author Singh, Ankita
Adam, Awadalkareem
Rodriguez, Leslie
Peng, Bi-Hung
Wang, Binbin
Xie, Xuping
Shi, Pei-Yong
Homma, Kohei
Wang, Tian
author_facet Singh, Ankita
Adam, Awadalkareem
Rodriguez, Leslie
Peng, Bi-Hung
Wang, Binbin
Xie, Xuping
Shi, Pei-Yong
Homma, Kohei
Wang, Tian
author_sort Singh, Ankita
collection PubMed
description The coronavirus disease 2019 (COVID-19) pandemic has significantly impacted global public health safety and the economy. Multiple antiviral drugs have been developed, and some have received regulatory approval and/or authorization. The use of nutraceuticals can be beneficial for preventing and treating COVID-19 complications. AHCC is a standardized, cultured extract of an edible mushroom Lentinula edodes of the Basidiomycete family of fungi that is enriched in acylated α-1,4-glucans. Here, we evaluated the effects of the oral administration of AHCC on the host response to SARS-CoV-2 infection in two murine models, K18-hACE2 transgenic mice and immunocompetent BALB/c mice. Oral administration of AHCC every other day for one week before and one day post SARS-CoV-2 infection in both strains of mice decreased the viral load and attenuated inflammation in the lungs. AHCC treatment also significantly reduced SARS-CoV-2-induced lethality in the K18-hACE2 mice. AHCC administration enhanced the expansion of γδ T cells in the spleen and lungs before and after viral infection and promoted T helper 1-prone mucosal and systemic T cell responses in both models. In AHCC-fed BALB/c mice, SARS-CoV-2 specific IgG responses were also enhanced. In summary, AHCC supplementation enhances host resistance against mild and severe COVID-19 infection primarily via the promotion of innate and adaptive T cell immune responses in mice.
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spelling pubmed-101442962023-04-29 Oral Supplementation with AHCC(®), a Standardized Extract of Cultured Lentinula edodes Mycelia, Enhances Host Resistance against SARS-CoV-2 Infection Singh, Ankita Adam, Awadalkareem Rodriguez, Leslie Peng, Bi-Hung Wang, Binbin Xie, Xuping Shi, Pei-Yong Homma, Kohei Wang, Tian Pathogens Article The coronavirus disease 2019 (COVID-19) pandemic has significantly impacted global public health safety and the economy. Multiple antiviral drugs have been developed, and some have received regulatory approval and/or authorization. The use of nutraceuticals can be beneficial for preventing and treating COVID-19 complications. AHCC is a standardized, cultured extract of an edible mushroom Lentinula edodes of the Basidiomycete family of fungi that is enriched in acylated α-1,4-glucans. Here, we evaluated the effects of the oral administration of AHCC on the host response to SARS-CoV-2 infection in two murine models, K18-hACE2 transgenic mice and immunocompetent BALB/c mice. Oral administration of AHCC every other day for one week before and one day post SARS-CoV-2 infection in both strains of mice decreased the viral load and attenuated inflammation in the lungs. AHCC treatment also significantly reduced SARS-CoV-2-induced lethality in the K18-hACE2 mice. AHCC administration enhanced the expansion of γδ T cells in the spleen and lungs before and after viral infection and promoted T helper 1-prone mucosal and systemic T cell responses in both models. In AHCC-fed BALB/c mice, SARS-CoV-2 specific IgG responses were also enhanced. In summary, AHCC supplementation enhances host resistance against mild and severe COVID-19 infection primarily via the promotion of innate and adaptive T cell immune responses in mice. MDPI 2023-04-03 /pmc/articles/PMC10144296/ /pubmed/37111440 http://dx.doi.org/10.3390/pathogens12040554 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Singh, Ankita
Adam, Awadalkareem
Rodriguez, Leslie
Peng, Bi-Hung
Wang, Binbin
Xie, Xuping
Shi, Pei-Yong
Homma, Kohei
Wang, Tian
Oral Supplementation with AHCC(®), a Standardized Extract of Cultured Lentinula edodes Mycelia, Enhances Host Resistance against SARS-CoV-2 Infection
title Oral Supplementation with AHCC(®), a Standardized Extract of Cultured Lentinula edodes Mycelia, Enhances Host Resistance against SARS-CoV-2 Infection
title_full Oral Supplementation with AHCC(®), a Standardized Extract of Cultured Lentinula edodes Mycelia, Enhances Host Resistance against SARS-CoV-2 Infection
title_fullStr Oral Supplementation with AHCC(®), a Standardized Extract of Cultured Lentinula edodes Mycelia, Enhances Host Resistance against SARS-CoV-2 Infection
title_full_unstemmed Oral Supplementation with AHCC(®), a Standardized Extract of Cultured Lentinula edodes Mycelia, Enhances Host Resistance against SARS-CoV-2 Infection
title_short Oral Supplementation with AHCC(®), a Standardized Extract of Cultured Lentinula edodes Mycelia, Enhances Host Resistance against SARS-CoV-2 Infection
title_sort oral supplementation with ahcc(®), a standardized extract of cultured lentinula edodes mycelia, enhances host resistance against sars-cov-2 infection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10144296/
https://www.ncbi.nlm.nih.gov/pubmed/37111440
http://dx.doi.org/10.3390/pathogens12040554
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