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Exploiting B Cell Transfer for Cancer Therapy: Engineered B Cells to Eradicate Tumors
Nowadays, cancers still represent a significant health burden, accounting for around 10 million deaths per year, due to ageing populations and inefficient treatments for some refractory cancers. Immunotherapy strategies that modulate the patient’s immune system have emerged as good treatment options...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8468294/ https://www.ncbi.nlm.nih.gov/pubmed/34576154 http://dx.doi.org/10.3390/ijms22189991 |
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author | Page, Audrey Hubert, Julie Fusil, Floriane Cosset, François-Loïc |
author_facet | Page, Audrey Hubert, Julie Fusil, Floriane Cosset, François-Loïc |
author_sort | Page, Audrey |
collection | PubMed |
description | Nowadays, cancers still represent a significant health burden, accounting for around 10 million deaths per year, due to ageing populations and inefficient treatments for some refractory cancers. Immunotherapy strategies that modulate the patient’s immune system have emerged as good treatment options. Among them, the adoptive transfer of B cells selected ex vivo showed promising results, with a reduction in tumor growth in several cancer mouse models, often associated with antitumoral immune responses. Aside from the benefits of their intrinsic properties, including antigen presentation, antibody secretion, homing and long-term persistence, B cells can be modified prior to reinfusion to increase their therapeutic role. For instance, B cells have been modified mainly to boost their immuno-stimulatory activation potential by forcing the expression of costimulatory ligands using defined culture conditions or gene insertion. Moreover, tumor-specific antigen presentation by infused B cells has been increased by ex vivo antigen loading (peptides, RNA, DNA, virus) or by the sorting/ engineering of B cells with a B cell receptor specific to tumor antigens. Editing of the BCR also rewires B cell specificity toward tumor antigens, and may trigger, upon antigen recognition, the secretion of antitumor antibodies by differentiated plasma cells that can then be recognized by other immune components or cells involved in tumor clearance by antibody-dependent cell cytotoxicity or complement-dependent cytotoxicity for example. With the expansion of gene editing methodologies, new strategies to reprogram immune cells with whole synthetic circuits are being explored: modified B cells can sense disease-specific biomarkers and, in response, trigger the expression of therapeutic molecules, such as molecules that counteract the tumoral immunosuppressive microenvironment. Such strategies remain in their infancy for implementation in B cells, but are likely to expand in the coming years. |
format | Online Article Text |
id | pubmed-8468294 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-84682942021-09-27 Exploiting B Cell Transfer for Cancer Therapy: Engineered B Cells to Eradicate Tumors Page, Audrey Hubert, Julie Fusil, Floriane Cosset, François-Loïc Int J Mol Sci Review Nowadays, cancers still represent a significant health burden, accounting for around 10 million deaths per year, due to ageing populations and inefficient treatments for some refractory cancers. Immunotherapy strategies that modulate the patient’s immune system have emerged as good treatment options. Among them, the adoptive transfer of B cells selected ex vivo showed promising results, with a reduction in tumor growth in several cancer mouse models, often associated with antitumoral immune responses. Aside from the benefits of their intrinsic properties, including antigen presentation, antibody secretion, homing and long-term persistence, B cells can be modified prior to reinfusion to increase their therapeutic role. For instance, B cells have been modified mainly to boost their immuno-stimulatory activation potential by forcing the expression of costimulatory ligands using defined culture conditions or gene insertion. Moreover, tumor-specific antigen presentation by infused B cells has been increased by ex vivo antigen loading (peptides, RNA, DNA, virus) or by the sorting/ engineering of B cells with a B cell receptor specific to tumor antigens. Editing of the BCR also rewires B cell specificity toward tumor antigens, and may trigger, upon antigen recognition, the secretion of antitumor antibodies by differentiated plasma cells that can then be recognized by other immune components or cells involved in tumor clearance by antibody-dependent cell cytotoxicity or complement-dependent cytotoxicity for example. With the expansion of gene editing methodologies, new strategies to reprogram immune cells with whole synthetic circuits are being explored: modified B cells can sense disease-specific biomarkers and, in response, trigger the expression of therapeutic molecules, such as molecules that counteract the tumoral immunosuppressive microenvironment. Such strategies remain in their infancy for implementation in B cells, but are likely to expand in the coming years. MDPI 2021-09-16 /pmc/articles/PMC8468294/ /pubmed/34576154 http://dx.doi.org/10.3390/ijms22189991 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Page, Audrey Hubert, Julie Fusil, Floriane Cosset, François-Loïc Exploiting B Cell Transfer for Cancer Therapy: Engineered B Cells to Eradicate Tumors |
title | Exploiting B Cell Transfer for Cancer Therapy: Engineered B Cells to Eradicate Tumors |
title_full | Exploiting B Cell Transfer for Cancer Therapy: Engineered B Cells to Eradicate Tumors |
title_fullStr | Exploiting B Cell Transfer for Cancer Therapy: Engineered B Cells to Eradicate Tumors |
title_full_unstemmed | Exploiting B Cell Transfer for Cancer Therapy: Engineered B Cells to Eradicate Tumors |
title_short | Exploiting B Cell Transfer for Cancer Therapy: Engineered B Cells to Eradicate Tumors |
title_sort | exploiting b cell transfer for cancer therapy: engineered b cells to eradicate tumors |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8468294/ https://www.ncbi.nlm.nih.gov/pubmed/34576154 http://dx.doi.org/10.3390/ijms22189991 |
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