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Soluble CD80 oral delivery by recombinant Lactococcus suppresses tumor growth by enhancing antitumor immunity

CD80 is an important co‐stimulatory molecule that participates in the immune response. Soluble CD80 can induce T cell activation and overcome PDL1‐mediated immune suppression. In this study, we aimed to construct recombinant Lactococcus lactis for oral delivery of the soluble CD80 (hsCD80) protein o...

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Autores principales: Lin, Ziqing, Tang, Yanqing, Chen, Zerong, Li, Simin, Xu, Xueyan, Hou, Xufeng, Chen, Zhenhui, Wen, Junjie, Zeng, Weisen, Meng, Xiaojing, Fan, Hongying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10354755/
https://www.ncbi.nlm.nih.gov/pubmed/37476068
http://dx.doi.org/10.1002/btm2.10533
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author Lin, Ziqing
Tang, Yanqing
Chen, Zerong
Li, Simin
Xu, Xueyan
Hou, Xufeng
Chen, Zhenhui
Wen, Junjie
Zeng, Weisen
Meng, Xiaojing
Fan, Hongying
author_facet Lin, Ziqing
Tang, Yanqing
Chen, Zerong
Li, Simin
Xu, Xueyan
Hou, Xufeng
Chen, Zhenhui
Wen, Junjie
Zeng, Weisen
Meng, Xiaojing
Fan, Hongying
author_sort Lin, Ziqing
collection PubMed
description CD80 is an important co‐stimulatory molecule that participates in the immune response. Soluble CD80 can induce T cell activation and overcome PDL1‐mediated immune suppression. In this study, we aimed to construct recombinant Lactococcus lactis for oral delivery of the soluble CD80 (hsCD80) protein or the fusion protein containing the cholera toxin B subunit (CTB) and hsCD80 (CTB‐hsCD80) under the control of the nisin‐inducible expression system. The recombinant L. lactis expressed and secreted hsCD80 or CTB‐hsCD80 fusion proteins after induction by nisin in vitro and in the enteric cavity. Additionally, the CTB‐hsCD80 fusion protein showed uptake by intestinal epithelial cells, was cleaved by the furin protease, and was released as free hsCD80 protein into the blood circulation. Orally administered hsCD80 and CTB‐hsCD80 containing L. lactis increased the proportion of activated T cells in the spleen and intestinal epithelium, inhibited tumor growth, and prolonged the survival of tumor‐bearing mice. The hsCD80‐containing L. lactis showed greater therapeutic effects on primary colonic adenoma in APC(min/−) mice and completely suppressed tumor growth. Further, recombinant CTB‐hsCD80 in L. lactis was more efficient than hsCD80‐containing bacteria in inhibiting the growth of xenografted colon cancer and melanoma cells. hsCD80 engineered probiotics may serve as a promising new approach for antitumor immunotherapy, especially for colorectal cancer.
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spelling pubmed-103547552023-07-20 Soluble CD80 oral delivery by recombinant Lactococcus suppresses tumor growth by enhancing antitumor immunity Lin, Ziqing Tang, Yanqing Chen, Zerong Li, Simin Xu, Xueyan Hou, Xufeng Chen, Zhenhui Wen, Junjie Zeng, Weisen Meng, Xiaojing Fan, Hongying Bioeng Transl Med Research Articles CD80 is an important co‐stimulatory molecule that participates in the immune response. Soluble CD80 can induce T cell activation and overcome PDL1‐mediated immune suppression. In this study, we aimed to construct recombinant Lactococcus lactis for oral delivery of the soluble CD80 (hsCD80) protein or the fusion protein containing the cholera toxin B subunit (CTB) and hsCD80 (CTB‐hsCD80) under the control of the nisin‐inducible expression system. The recombinant L. lactis expressed and secreted hsCD80 or CTB‐hsCD80 fusion proteins after induction by nisin in vitro and in the enteric cavity. Additionally, the CTB‐hsCD80 fusion protein showed uptake by intestinal epithelial cells, was cleaved by the furin protease, and was released as free hsCD80 protein into the blood circulation. Orally administered hsCD80 and CTB‐hsCD80 containing L. lactis increased the proportion of activated T cells in the spleen and intestinal epithelium, inhibited tumor growth, and prolonged the survival of tumor‐bearing mice. The hsCD80‐containing L. lactis showed greater therapeutic effects on primary colonic adenoma in APC(min/−) mice and completely suppressed tumor growth. Further, recombinant CTB‐hsCD80 in L. lactis was more efficient than hsCD80‐containing bacteria in inhibiting the growth of xenografted colon cancer and melanoma cells. hsCD80 engineered probiotics may serve as a promising new approach for antitumor immunotherapy, especially for colorectal cancer. John Wiley & Sons, Inc. 2023-05-03 /pmc/articles/PMC10354755/ /pubmed/37476068 http://dx.doi.org/10.1002/btm2.10533 Text en © 2023 The Authors. Bioengineering & Translational Medicine published by Wiley Periodicals LLC on behalf of American Institute of Chemical Engineers. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Lin, Ziqing
Tang, Yanqing
Chen, Zerong
Li, Simin
Xu, Xueyan
Hou, Xufeng
Chen, Zhenhui
Wen, Junjie
Zeng, Weisen
Meng, Xiaojing
Fan, Hongying
Soluble CD80 oral delivery by recombinant Lactococcus suppresses tumor growth by enhancing antitumor immunity
title Soluble CD80 oral delivery by recombinant Lactococcus suppresses tumor growth by enhancing antitumor immunity
title_full Soluble CD80 oral delivery by recombinant Lactococcus suppresses tumor growth by enhancing antitumor immunity
title_fullStr Soluble CD80 oral delivery by recombinant Lactococcus suppresses tumor growth by enhancing antitumor immunity
title_full_unstemmed Soluble CD80 oral delivery by recombinant Lactococcus suppresses tumor growth by enhancing antitumor immunity
title_short Soluble CD80 oral delivery by recombinant Lactococcus suppresses tumor growth by enhancing antitumor immunity
title_sort soluble cd80 oral delivery by recombinant lactococcus suppresses tumor growth by enhancing antitumor immunity
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10354755/
https://www.ncbi.nlm.nih.gov/pubmed/37476068
http://dx.doi.org/10.1002/btm2.10533
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