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Worked to the bone: antibody-based conditioning as the future of transplant biology
Conditioning of the bone marrow prior to haematopoietic stem cell transplant is essential in eradicating the primary cause of disease, facilitating donor cell engraftment and avoiding transplant rejection via immunosuppression. Standard conditioning regimens, typically comprising chemotherapy and/or...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9118867/ https://www.ncbi.nlm.nih.gov/pubmed/35590415 http://dx.doi.org/10.1186/s13045-022-01284-6 |
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author | Griffin, James M. Healy, Fiona M. Dahal, Lekh N. Floisand, Yngvar Woolley, John F. |
author_facet | Griffin, James M. Healy, Fiona M. Dahal, Lekh N. Floisand, Yngvar Woolley, John F. |
author_sort | Griffin, James M. |
collection | PubMed |
description | Conditioning of the bone marrow prior to haematopoietic stem cell transplant is essential in eradicating the primary cause of disease, facilitating donor cell engraftment and avoiding transplant rejection via immunosuppression. Standard conditioning regimens, typically comprising chemotherapy and/or radiotherapy, have proven successful in bone marrow clearance but are also associated with severe toxicities and high incidence of treatment-related mortality. Antibody-based conditioning is a developing field which, thus far, has largely shown an improved toxicity profile in experimental models and improved transplant outcomes, compared to traditional conditioning. Most antibody-based conditioning therapies involve monoclonal/naked antibodies, such as alemtuzumab for graft-versus-host disease prophylaxis and rituximab for Epstein–Barr virus prophylaxis, which are both in Phase II trials for inclusion in conditioning regimens. Nevertheless, alternative immune-based therapies, including antibody–drug conjugates, radio-labelled antibodies and CAR-T cells, are showing promise in a conditioning setting. Here, we analyse the current status of antibody-based drugs in pre-transplant conditioning regimens and assess their potential in the future of transplant biology. |
format | Online Article Text |
id | pubmed-9118867 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-91188672022-05-20 Worked to the bone: antibody-based conditioning as the future of transplant biology Griffin, James M. Healy, Fiona M. Dahal, Lekh N. Floisand, Yngvar Woolley, John F. J Hematol Oncol Review Conditioning of the bone marrow prior to haematopoietic stem cell transplant is essential in eradicating the primary cause of disease, facilitating donor cell engraftment and avoiding transplant rejection via immunosuppression. Standard conditioning regimens, typically comprising chemotherapy and/or radiotherapy, have proven successful in bone marrow clearance but are also associated with severe toxicities and high incidence of treatment-related mortality. Antibody-based conditioning is a developing field which, thus far, has largely shown an improved toxicity profile in experimental models and improved transplant outcomes, compared to traditional conditioning. Most antibody-based conditioning therapies involve monoclonal/naked antibodies, such as alemtuzumab for graft-versus-host disease prophylaxis and rituximab for Epstein–Barr virus prophylaxis, which are both in Phase II trials for inclusion in conditioning regimens. Nevertheless, alternative immune-based therapies, including antibody–drug conjugates, radio-labelled antibodies and CAR-T cells, are showing promise in a conditioning setting. Here, we analyse the current status of antibody-based drugs in pre-transplant conditioning regimens and assess their potential in the future of transplant biology. BioMed Central 2022-05-19 /pmc/articles/PMC9118867/ /pubmed/35590415 http://dx.doi.org/10.1186/s13045-022-01284-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Review Griffin, James M. Healy, Fiona M. Dahal, Lekh N. Floisand, Yngvar Woolley, John F. Worked to the bone: antibody-based conditioning as the future of transplant biology |
title | Worked to the bone: antibody-based conditioning as the future of transplant biology |
title_full | Worked to the bone: antibody-based conditioning as the future of transplant biology |
title_fullStr | Worked to the bone: antibody-based conditioning as the future of transplant biology |
title_full_unstemmed | Worked to the bone: antibody-based conditioning as the future of transplant biology |
title_short | Worked to the bone: antibody-based conditioning as the future of transplant biology |
title_sort | worked to the bone: antibody-based conditioning as the future of transplant biology |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9118867/ https://www.ncbi.nlm.nih.gov/pubmed/35590415 http://dx.doi.org/10.1186/s13045-022-01284-6 |
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