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A novel prostate cancer immunotherapy using prostate-specific antigen peptides and Candida skin test reagent as an adjuvant

OBJECTIVES: Our group developed the use of the Candida skin test reagent as an adjuvant of cell-mediated immunity in designing a human papillomavirus therapeutic vaccine. Here, this technology is being applied for designing a prostate cancer immunotherapy. METHODS: Peptides based on the prostate-spe...

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Autores principales: Abdallah, Al-Ola, Coleman, Hannah, Kamel, Mohamed, Davis, Rodney, Landrum, Teri, Spencer, Horace, Mackintosh, Sam, Mahmoud, Fade A, Milojkovic, Natasa, Wicker, Chester, Arnaoutakis, Konstantinos, Nakagawa, Mayumi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6144584/
https://www.ncbi.nlm.nih.gov/pubmed/30245818
http://dx.doi.org/10.1177/2050312118800202
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author Abdallah, Al-Ola
Coleman, Hannah
Kamel, Mohamed
Davis, Rodney
Landrum, Teri
Spencer, Horace
Mackintosh, Sam
Mahmoud, Fade A
Milojkovic, Natasa
Wicker, Chester
Arnaoutakis, Konstantinos
Nakagawa, Mayumi
author_facet Abdallah, Al-Ola
Coleman, Hannah
Kamel, Mohamed
Davis, Rodney
Landrum, Teri
Spencer, Horace
Mackintosh, Sam
Mahmoud, Fade A
Milojkovic, Natasa
Wicker, Chester
Arnaoutakis, Konstantinos
Nakagawa, Mayumi
author_sort Abdallah, Al-Ola
collection PubMed
description OBJECTIVES: Our group developed the use of the Candida skin test reagent as an adjuvant of cell-mediated immunity in designing a human papillomavirus therapeutic vaccine. Here, this technology is being applied for designing a prostate cancer immunotherapy. METHODS: Peptides based on the prostate-specific antigen amino acid sequences were selected, synthesized, and evaluated in terms of their (1) solubility, (2) maturation effects on Langerhans cells by fluorescence-activated cell sorter analysis, and (3) recognition by peripheral immune cells from prostate cancer patients using interferon-γ enzyme-linked immunospot assay. RESULTS: The peptides were soluble in 10 mM succinate at pH of 5 with 5% glycine, and they demonstrated no maturation effects on Langerhans cells from healthy donors. On the other hand, peripheral immune cells from 4 of 10 prostate cancer patients examined had positive responses in enzyme-linked immunospot assay to one or more prostate-specific antigen peptides. CONCLUSION: In summary, a design and a formulation of a novel prostate cancer immunotherapy are described. The immunogenicity of prostate-specific antigen peptides in some prostate cancer patients supports further development of this immunotherapy.
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spelling pubmed-61445842018-09-21 A novel prostate cancer immunotherapy using prostate-specific antigen peptides and Candida skin test reagent as an adjuvant Abdallah, Al-Ola Coleman, Hannah Kamel, Mohamed Davis, Rodney Landrum, Teri Spencer, Horace Mackintosh, Sam Mahmoud, Fade A Milojkovic, Natasa Wicker, Chester Arnaoutakis, Konstantinos Nakagawa, Mayumi SAGE Open Med Original Article OBJECTIVES: Our group developed the use of the Candida skin test reagent as an adjuvant of cell-mediated immunity in designing a human papillomavirus therapeutic vaccine. Here, this technology is being applied for designing a prostate cancer immunotherapy. METHODS: Peptides based on the prostate-specific antigen amino acid sequences were selected, synthesized, and evaluated in terms of their (1) solubility, (2) maturation effects on Langerhans cells by fluorescence-activated cell sorter analysis, and (3) recognition by peripheral immune cells from prostate cancer patients using interferon-γ enzyme-linked immunospot assay. RESULTS: The peptides were soluble in 10 mM succinate at pH of 5 with 5% glycine, and they demonstrated no maturation effects on Langerhans cells from healthy donors. On the other hand, peripheral immune cells from 4 of 10 prostate cancer patients examined had positive responses in enzyme-linked immunospot assay to one or more prostate-specific antigen peptides. CONCLUSION: In summary, a design and a formulation of a novel prostate cancer immunotherapy are described. The immunogenicity of prostate-specific antigen peptides in some prostate cancer patients supports further development of this immunotherapy. SAGE Publications 2018-09-17 /pmc/articles/PMC6144584/ /pubmed/30245818 http://dx.doi.org/10.1177/2050312118800202 Text en © The Author(s) 2018 http://www.creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Article
Abdallah, Al-Ola
Coleman, Hannah
Kamel, Mohamed
Davis, Rodney
Landrum, Teri
Spencer, Horace
Mackintosh, Sam
Mahmoud, Fade A
Milojkovic, Natasa
Wicker, Chester
Arnaoutakis, Konstantinos
Nakagawa, Mayumi
A novel prostate cancer immunotherapy using prostate-specific antigen peptides and Candida skin test reagent as an adjuvant
title A novel prostate cancer immunotherapy using prostate-specific antigen peptides and Candida skin test reagent as an adjuvant
title_full A novel prostate cancer immunotherapy using prostate-specific antigen peptides and Candida skin test reagent as an adjuvant
title_fullStr A novel prostate cancer immunotherapy using prostate-specific antigen peptides and Candida skin test reagent as an adjuvant
title_full_unstemmed A novel prostate cancer immunotherapy using prostate-specific antigen peptides and Candida skin test reagent as an adjuvant
title_short A novel prostate cancer immunotherapy using prostate-specific antigen peptides and Candida skin test reagent as an adjuvant
title_sort novel prostate cancer immunotherapy using prostate-specific antigen peptides and candida skin test reagent as an adjuvant
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6144584/
https://www.ncbi.nlm.nih.gov/pubmed/30245818
http://dx.doi.org/10.1177/2050312118800202
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