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A randomized double blinded placebo controlled clinical trial for the evaluation of green coffee extract on immune health in healthy adults
BACKGROUND: The immune system functions to protect the host from a broad array of infectious diseases. Here, we evaluated the in vitro immunomodulatory effects of green coffee extract (GCE), and conducted a double-blinded, randomized and placebo-controlled trial among apparently healthy individuals....
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9446042/ https://www.ncbi.nlm.nih.gov/pubmed/36081816 http://dx.doi.org/10.1016/j.jtcme.2022.01.007 |
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author | Narayanaperumal, Jeyaparthasarathy D'souza, Avin Miriyala, Amarnath Sharma, Bhavna Gopal, Ganesh |
author_facet | Narayanaperumal, Jeyaparthasarathy D'souza, Avin Miriyala, Amarnath Sharma, Bhavna Gopal, Ganesh |
author_sort | Narayanaperumal, Jeyaparthasarathy |
collection | PubMed |
description | BACKGROUND: The immune system functions to protect the host from a broad array of infectious diseases. Here, we evaluated the in vitro immunomodulatory effects of green coffee extract (GCE), and conducted a double-blinded, randomized and placebo-controlled trial among apparently healthy individuals. METHODS: We determined the levels and functions of inflammatory and immune markers viz., phospho-NF-κB p65 ser536, chemotaxis, phagocytosis, TH1/TH2 cytokines and IgG production. We also evaluated several immunological markers such as total leukocyte counts, differential leukocyte counts, NK cell activity, CD4/CD8 ratio, serum immunoglobulin, C-reactive protein (CRP) and pro-inflammatory cytokines (IL-6 and TNF-α). RESULTS AND CONCLUSION: GCE significantly inhibited LPS-induced NF-κB p65 ser536 phosphorylation, MCP-1-induced chemotaxis and significantly enhanced phagocytosis and IgG production. In addition, GCE modulated PMA/PHA-induced TH1/TH2 cytokine production. Clinical investigations suggested that the expression of CD56 and CD16 was markedly augmented on NK cells following GCE treatment. GCE significantly enhanced IgA production before and after influenza vaccination. Similarly, IL-6, TNF-α and CRP levels were significantly inhibited by GCE. Together, GCE confers several salubrious immunomodulatory effects at different levels attributing to optimal functioning of immune responses in the host. TAXONOMY: Cell biology, Clinical study, Clinical Trial. |
format | Online Article Text |
id | pubmed-9446042 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-94460422022-09-07 A randomized double blinded placebo controlled clinical trial for the evaluation of green coffee extract on immune health in healthy adults Narayanaperumal, Jeyaparthasarathy D'souza, Avin Miriyala, Amarnath Sharma, Bhavna Gopal, Ganesh J Tradit Complement Med Article BACKGROUND: The immune system functions to protect the host from a broad array of infectious diseases. Here, we evaluated the in vitro immunomodulatory effects of green coffee extract (GCE), and conducted a double-blinded, randomized and placebo-controlled trial among apparently healthy individuals. METHODS: We determined the levels and functions of inflammatory and immune markers viz., phospho-NF-κB p65 ser536, chemotaxis, phagocytosis, TH1/TH2 cytokines and IgG production. We also evaluated several immunological markers such as total leukocyte counts, differential leukocyte counts, NK cell activity, CD4/CD8 ratio, serum immunoglobulin, C-reactive protein (CRP) and pro-inflammatory cytokines (IL-6 and TNF-α). RESULTS AND CONCLUSION: GCE significantly inhibited LPS-induced NF-κB p65 ser536 phosphorylation, MCP-1-induced chemotaxis and significantly enhanced phagocytosis and IgG production. In addition, GCE modulated PMA/PHA-induced TH1/TH2 cytokine production. Clinical investigations suggested that the expression of CD56 and CD16 was markedly augmented on NK cells following GCE treatment. GCE significantly enhanced IgA production before and after influenza vaccination. Similarly, IL-6, TNF-α and CRP levels were significantly inhibited by GCE. Together, GCE confers several salubrious immunomodulatory effects at different levels attributing to optimal functioning of immune responses in the host. TAXONOMY: Cell biology, Clinical study, Clinical Trial. Elsevier 2022-02-02 /pmc/articles/PMC9446042/ /pubmed/36081816 http://dx.doi.org/10.1016/j.jtcme.2022.01.007 Text en © 2022 Center for Food and Biomolecules, National Taiwan University. Production and hosting by Elsevier Taiwan LLC. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Narayanaperumal, Jeyaparthasarathy D'souza, Avin Miriyala, Amarnath Sharma, Bhavna Gopal, Ganesh A randomized double blinded placebo controlled clinical trial for the evaluation of green coffee extract on immune health in healthy adults |
title | A randomized double blinded placebo controlled clinical trial for the evaluation of green coffee extract on immune health in healthy adults |
title_full | A randomized double blinded placebo controlled clinical trial for the evaluation of green coffee extract on immune health in healthy adults |
title_fullStr | A randomized double blinded placebo controlled clinical trial for the evaluation of green coffee extract on immune health in healthy adults |
title_full_unstemmed | A randomized double blinded placebo controlled clinical trial for the evaluation of green coffee extract on immune health in healthy adults |
title_short | A randomized double blinded placebo controlled clinical trial for the evaluation of green coffee extract on immune health in healthy adults |
title_sort | randomized double blinded placebo controlled clinical trial for the evaluation of green coffee extract on immune health in healthy adults |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9446042/ https://www.ncbi.nlm.nih.gov/pubmed/36081816 http://dx.doi.org/10.1016/j.jtcme.2022.01.007 |
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