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Ars2‐containing bispecific, Fab‐ and IgG1‐format BAR‐bodies to target DLBCL cells
Despite recent advances in the therapy of diffuse large B‐cell lymphoma, not otherwise specified (DLBCL), around 30% of patients develop refractory disease or relapse after first‐line treatment. Recently, Ars2 was reported as the auto‐antigenic target of the B‐cell receptor (BCR) in approximately 25...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9928785/ https://www.ncbi.nlm.nih.gov/pubmed/36819155 http://dx.doi.org/10.1002/jha2.635 |
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author | Kiefer, Maximilian Thurner, Lorenz Bock, Theresa Cetin, Onur Kos, Igor Lesan, Vadim Kaddu‐Mulindwa, Dominic Bittenbring, Joerg Thomas Fadle, Natalie Regitz, Evi Hoth, Markus Neumann, Frank Preuss, Klaus‐Dieter Pfreundschuh, Michael Christofyllakis, Konstantinos Bewarder, Moritz |
author_facet | Kiefer, Maximilian Thurner, Lorenz Bock, Theresa Cetin, Onur Kos, Igor Lesan, Vadim Kaddu‐Mulindwa, Dominic Bittenbring, Joerg Thomas Fadle, Natalie Regitz, Evi Hoth, Markus Neumann, Frank Preuss, Klaus‐Dieter Pfreundschuh, Michael Christofyllakis, Konstantinos Bewarder, Moritz |
author_sort | Kiefer, Maximilian |
collection | PubMed |
description | Despite recent advances in the therapy of diffuse large B‐cell lymphoma, not otherwise specified (DLBCL), around 30% of patients develop refractory disease or relapse after first‐line treatment. Recently, Ars2 was reported as the auto‐antigenic target of the B‐cell receptor (BCR) in approximately 25% of activated B‐cell DLBCL cases. Ars2 could be used to specifically target B cells expressing Ars2‐reactive BCRs. However, the optimal therapeutic format to integrate Ars2 into has yet to be determined. To mimic therapeutic antibody formats, Ars2‐containing bispecific and IgG1‐like constructs (BCR antigens for reverse [BAR]‐bodies) were developed. Two bispecific BAR‐bodies connecting single‐chain antibodies against CD16 or CD3 to the BCR‐binding epitope of Ars2 were constructed. Both constructs showed strong binding to U2932 cells and induced effector cell‐dependent and selective cytotoxicity against U2932 cells of up to 44% at concentrations of 20 μg/ml. Additionally, IgG1‐format Ars2 BAR‐bodies were constructed by replacing the variable heavy‐ and light‐chain regions of a full‐length antibody with the Ars2 epitope. IgG1‐format Ars2 BAR‐bodies also bound selectively to U2932 and OCI‐Ly3 cells and induced selective cytotoxicity of up to 60% at 10 μg/ml. In conclusion, Ars2‐containing bispecific and IgG1‐format BAR‐bodies both are new therapeutic formats to target DLBCL cells. |
format | Online Article Text |
id | pubmed-9928785 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-99287852023-02-16 Ars2‐containing bispecific, Fab‐ and IgG1‐format BAR‐bodies to target DLBCL cells Kiefer, Maximilian Thurner, Lorenz Bock, Theresa Cetin, Onur Kos, Igor Lesan, Vadim Kaddu‐Mulindwa, Dominic Bittenbring, Joerg Thomas Fadle, Natalie Regitz, Evi Hoth, Markus Neumann, Frank Preuss, Klaus‐Dieter Pfreundschuh, Michael Christofyllakis, Konstantinos Bewarder, Moritz EJHaem Haematologic Malignancy ‐ Lymphoid Despite recent advances in the therapy of diffuse large B‐cell lymphoma, not otherwise specified (DLBCL), around 30% of patients develop refractory disease or relapse after first‐line treatment. Recently, Ars2 was reported as the auto‐antigenic target of the B‐cell receptor (BCR) in approximately 25% of activated B‐cell DLBCL cases. Ars2 could be used to specifically target B cells expressing Ars2‐reactive BCRs. However, the optimal therapeutic format to integrate Ars2 into has yet to be determined. To mimic therapeutic antibody formats, Ars2‐containing bispecific and IgG1‐like constructs (BCR antigens for reverse [BAR]‐bodies) were developed. Two bispecific BAR‐bodies connecting single‐chain antibodies against CD16 or CD3 to the BCR‐binding epitope of Ars2 were constructed. Both constructs showed strong binding to U2932 cells and induced effector cell‐dependent and selective cytotoxicity against U2932 cells of up to 44% at concentrations of 20 μg/ml. Additionally, IgG1‐format Ars2 BAR‐bodies were constructed by replacing the variable heavy‐ and light‐chain regions of a full‐length antibody with the Ars2 epitope. IgG1‐format Ars2 BAR‐bodies also bound selectively to U2932 and OCI‐Ly3 cells and induced selective cytotoxicity of up to 60% at 10 μg/ml. In conclusion, Ars2‐containing bispecific and IgG1‐format BAR‐bodies both are new therapeutic formats to target DLBCL cells. John Wiley and Sons Inc. 2022-12-27 /pmc/articles/PMC9928785/ /pubmed/36819155 http://dx.doi.org/10.1002/jha2.635 Text en © 2022 The Authors. eJHaem published by British Society for Haematology and John Wiley & Sons Ltd. 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 | Haematologic Malignancy ‐ Lymphoid Kiefer, Maximilian Thurner, Lorenz Bock, Theresa Cetin, Onur Kos, Igor Lesan, Vadim Kaddu‐Mulindwa, Dominic Bittenbring, Joerg Thomas Fadle, Natalie Regitz, Evi Hoth, Markus Neumann, Frank Preuss, Klaus‐Dieter Pfreundschuh, Michael Christofyllakis, Konstantinos Bewarder, Moritz Ars2‐containing bispecific, Fab‐ and IgG1‐format BAR‐bodies to target DLBCL cells |
title | Ars2‐containing bispecific, Fab‐ and IgG1‐format BAR‐bodies to target DLBCL cells |
title_full | Ars2‐containing bispecific, Fab‐ and IgG1‐format BAR‐bodies to target DLBCL cells |
title_fullStr | Ars2‐containing bispecific, Fab‐ and IgG1‐format BAR‐bodies to target DLBCL cells |
title_full_unstemmed | Ars2‐containing bispecific, Fab‐ and IgG1‐format BAR‐bodies to target DLBCL cells |
title_short | Ars2‐containing bispecific, Fab‐ and IgG1‐format BAR‐bodies to target DLBCL cells |
title_sort | ars2‐containing bispecific, fab‐ and igg1‐format bar‐bodies to target dlbcl cells |
topic | Haematologic Malignancy ‐ Lymphoid |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9928785/ https://www.ncbi.nlm.nih.gov/pubmed/36819155 http://dx.doi.org/10.1002/jha2.635 |
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