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Astragalus membranaceus–Derived Anti-Programmed Death-1 Monoclonal Antibodies with Immunomodulatory Therapeutic Effects against Tumors

Astragalus membranaceus polysaccharide (APS) components are main ingredients of TCM and have proven efficacy to activate T cells and B cells, enhancing immunity in humans. In this study, elevated cytokine and anti-PD-1 antibody titers were found in mice after immunization with APS. Therefore, phage-...

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Autores principales: Chang, Fu-Ling, Tsai, Keng-Chang, Lin, Tsai-Yu, Yang, Tz-Wen, Lo, Yan-Ni, Chen, Wang-Chuan, Chang, Jui-Hsien, Lu, Mei-Kuang, Chiou, Chun-Tang, Chen, Po-Hung, Yen, Yun, Pan, Shiow-Lin, Lee, Yu-Ching
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7073506/
https://www.ncbi.nlm.nih.gov/pubmed/32190660
http://dx.doi.org/10.1155/2020/3415471
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author Chang, Fu-Ling
Tsai, Keng-Chang
Lin, Tsai-Yu
Yang, Tz-Wen
Lo, Yan-Ni
Chen, Wang-Chuan
Chang, Jui-Hsien
Lu, Mei-Kuang
Chiou, Chun-Tang
Chen, Po-Hung
Yen, Yun
Pan, Shiow-Lin
Lee, Yu-Ching
author_facet Chang, Fu-Ling
Tsai, Keng-Chang
Lin, Tsai-Yu
Yang, Tz-Wen
Lo, Yan-Ni
Chen, Wang-Chuan
Chang, Jui-Hsien
Lu, Mei-Kuang
Chiou, Chun-Tang
Chen, Po-Hung
Yen, Yun
Pan, Shiow-Lin
Lee, Yu-Ching
author_sort Chang, Fu-Ling
collection PubMed
description Astragalus membranaceus polysaccharide (APS) components are main ingredients of TCM and have proven efficacy to activate T cells and B cells, enhancing immunity in humans. In this study, elevated cytokine and anti-PD-1 antibody titers were found in mice after immunization with APS. Therefore, phage-display technology was utilized to isolate specific anti-programmed death-1 (PD-1) antibodies from mice stimulated by APS and to confirm whether the isolated anti-PD-1 antibody could inhibit the interaction of PD-1 with the programmed death-ligand 1 (PD-L1), resulting in tumor growth inhibition. The isolated single-chain fragment variable (scFv) S12 exhibited the highest binding affinity of 20 nM to PD-1, completed the interaction between PD-1 and PD-L1, and blocked the effect of PD-L1-induced T cell exhaustion in peripheral blood mononuclear cells in vitro. In the animal model, the tumor growth inhibition effect after scFv S12 treatment was approximately 48%. However, meaningful synergistic effects were not observed when scFv S12 was used as a cotreatment with ixabepilone. Moreover, this treatment caused a reduction in the number of tumor-associated macrophages in the tumor tissue. These experimental results indirectly indicate the ability of APS to induce specific antibodies associated with the immune checkpoint system and the potential benefits for improving immunity in humans.
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spelling pubmed-70735062020-03-18 Astragalus membranaceus–Derived Anti-Programmed Death-1 Monoclonal Antibodies with Immunomodulatory Therapeutic Effects against Tumors Chang, Fu-Ling Tsai, Keng-Chang Lin, Tsai-Yu Yang, Tz-Wen Lo, Yan-Ni Chen, Wang-Chuan Chang, Jui-Hsien Lu, Mei-Kuang Chiou, Chun-Tang Chen, Po-Hung Yen, Yun Pan, Shiow-Lin Lee, Yu-Ching Biomed Res Int Research Article Astragalus membranaceus polysaccharide (APS) components are main ingredients of TCM and have proven efficacy to activate T cells and B cells, enhancing immunity in humans. In this study, elevated cytokine and anti-PD-1 antibody titers were found in mice after immunization with APS. Therefore, phage-display technology was utilized to isolate specific anti-programmed death-1 (PD-1) antibodies from mice stimulated by APS and to confirm whether the isolated anti-PD-1 antibody could inhibit the interaction of PD-1 with the programmed death-ligand 1 (PD-L1), resulting in tumor growth inhibition. The isolated single-chain fragment variable (scFv) S12 exhibited the highest binding affinity of 20 nM to PD-1, completed the interaction between PD-1 and PD-L1, and blocked the effect of PD-L1-induced T cell exhaustion in peripheral blood mononuclear cells in vitro. In the animal model, the tumor growth inhibition effect after scFv S12 treatment was approximately 48%. However, meaningful synergistic effects were not observed when scFv S12 was used as a cotreatment with ixabepilone. Moreover, this treatment caused a reduction in the number of tumor-associated macrophages in the tumor tissue. These experimental results indirectly indicate the ability of APS to induce specific antibodies associated with the immune checkpoint system and the potential benefits for improving immunity in humans. Hindawi 2020-03-03 /pmc/articles/PMC7073506/ /pubmed/32190660 http://dx.doi.org/10.1155/2020/3415471 Text en Copyright © 2020 Fu-Ling Chang et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Chang, Fu-Ling
Tsai, Keng-Chang
Lin, Tsai-Yu
Yang, Tz-Wen
Lo, Yan-Ni
Chen, Wang-Chuan
Chang, Jui-Hsien
Lu, Mei-Kuang
Chiou, Chun-Tang
Chen, Po-Hung
Yen, Yun
Pan, Shiow-Lin
Lee, Yu-Ching
Astragalus membranaceus–Derived Anti-Programmed Death-1 Monoclonal Antibodies with Immunomodulatory Therapeutic Effects against Tumors
title Astragalus membranaceus–Derived Anti-Programmed Death-1 Monoclonal Antibodies with Immunomodulatory Therapeutic Effects against Tumors
title_full Astragalus membranaceus–Derived Anti-Programmed Death-1 Monoclonal Antibodies with Immunomodulatory Therapeutic Effects against Tumors
title_fullStr Astragalus membranaceus–Derived Anti-Programmed Death-1 Monoclonal Antibodies with Immunomodulatory Therapeutic Effects against Tumors
title_full_unstemmed Astragalus membranaceus–Derived Anti-Programmed Death-1 Monoclonal Antibodies with Immunomodulatory Therapeutic Effects against Tumors
title_short Astragalus membranaceus–Derived Anti-Programmed Death-1 Monoclonal Antibodies with Immunomodulatory Therapeutic Effects against Tumors
title_sort astragalus membranaceus–derived anti-programmed death-1 monoclonal antibodies with immunomodulatory therapeutic effects against tumors
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7073506/
https://www.ncbi.nlm.nih.gov/pubmed/32190660
http://dx.doi.org/10.1155/2020/3415471
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