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Amphotericin B, an Anti-Fungal Medication, Directly Increases the Cytotoxicity of NK Cells

Immunomodulatory drugs (IMiDs) present one example of immunomodulatory agents that improve cancer immunotherapy. Based on the cytotoxic activity of natural killer (NK) cells against cancer cells, a high throughput screening method for the identification of novel immunomodulatory molecules with the p...

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Detalles Bibliográficos
Autores principales: Kim, Nayoung, Choi, Ji-Wan, Park, Hye-Ran, Kim, Inki, Kim, Hun Sik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5486084/
https://www.ncbi.nlm.nih.gov/pubmed/28608807
http://dx.doi.org/10.3390/ijms18061262
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author Kim, Nayoung
Choi, Ji-Wan
Park, Hye-Ran
Kim, Inki
Kim, Hun Sik
author_facet Kim, Nayoung
Choi, Ji-Wan
Park, Hye-Ran
Kim, Inki
Kim, Hun Sik
author_sort Kim, Nayoung
collection PubMed
description Immunomodulatory drugs (IMiDs) present one example of immunomodulatory agents that improve cancer immunotherapy. Based on the cytotoxic activity of natural killer (NK) cells against cancer cells, a high throughput screening method for the identification of novel immunomodulatory molecules with the potential to stimulate NK cell cytotoxicity against cancer cells was designed and tested using an approved drug library. Among the primary hit compounds, the anti-fungal drug amphotericin B (AMP-B) increased the cytotoxicity of NK cell line and human primary NK cells in a direct manner. The increase in NK cell activity was related to increased formation of NK-target cell conjugates and the subsequent granule polarization toward target cells. The results of the present study indicate that AMP-B could serve a dual function as an anti-fungal and immunomodulatory drug.
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spelling pubmed-54860842017-06-29 Amphotericin B, an Anti-Fungal Medication, Directly Increases the Cytotoxicity of NK Cells Kim, Nayoung Choi, Ji-Wan Park, Hye-Ran Kim, Inki Kim, Hun Sik Int J Mol Sci Article Immunomodulatory drugs (IMiDs) present one example of immunomodulatory agents that improve cancer immunotherapy. Based on the cytotoxic activity of natural killer (NK) cells against cancer cells, a high throughput screening method for the identification of novel immunomodulatory molecules with the potential to stimulate NK cell cytotoxicity against cancer cells was designed and tested using an approved drug library. Among the primary hit compounds, the anti-fungal drug amphotericin B (AMP-B) increased the cytotoxicity of NK cell line and human primary NK cells in a direct manner. The increase in NK cell activity was related to increased formation of NK-target cell conjugates and the subsequent granule polarization toward target cells. The results of the present study indicate that AMP-B could serve a dual function as an anti-fungal and immunomodulatory drug. MDPI 2017-06-13 /pmc/articles/PMC5486084/ /pubmed/28608807 http://dx.doi.org/10.3390/ijms18061262 Text en © 2017 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kim, Nayoung
Choi, Ji-Wan
Park, Hye-Ran
Kim, Inki
Kim, Hun Sik
Amphotericin B, an Anti-Fungal Medication, Directly Increases the Cytotoxicity of NK Cells
title Amphotericin B, an Anti-Fungal Medication, Directly Increases the Cytotoxicity of NK Cells
title_full Amphotericin B, an Anti-Fungal Medication, Directly Increases the Cytotoxicity of NK Cells
title_fullStr Amphotericin B, an Anti-Fungal Medication, Directly Increases the Cytotoxicity of NK Cells
title_full_unstemmed Amphotericin B, an Anti-Fungal Medication, Directly Increases the Cytotoxicity of NK Cells
title_short Amphotericin B, an Anti-Fungal Medication, Directly Increases the Cytotoxicity of NK Cells
title_sort amphotericin b, an anti-fungal medication, directly increases the cytotoxicity of nk cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5486084/
https://www.ncbi.nlm.nih.gov/pubmed/28608807
http://dx.doi.org/10.3390/ijms18061262
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