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The challenges of translation
Cancer immunotherapy is a highly active area in translational medicine where the challenges and rewards of developing new drugs “from bench to bedside” become particularly visible. Here, we comment on both, the scientific and non‐scientific hurdles of this translational process using the example of...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6895598/ https://www.ncbi.nlm.nih.gov/pubmed/31625285 http://dx.doi.org/10.15252/emmm.201910874 |
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author | Salih, Helmut R Jung, Gundram |
author_facet | Salih, Helmut R Jung, Gundram |
author_sort | Salih, Helmut R |
collection | PubMed |
description | Cancer immunotherapy is a highly active area in translational medicine where the challenges and rewards of developing new drugs “from bench to bedside” become particularly visible. Here, we comment on both, the scientific and non‐scientific hurdles of this translational process using the example of bispecific antibodies (bsAbs) and chimeric antigen receptor (CAR) T cells, two closely related strategies for antibody‐guided recruitment of T cells against cancer. Both exert impressive therapeutic activity and were recently approved for treatment of B‐cell malignancies. We discuss how the efficacy of these auspicious therapeutic tools may be further improved, in particular against solid tumors, but we also address another critical issue: Since both approaches were already introduced in the 1980s, why did it take almost thirty years until they became clinically available? |
format | Online Article Text |
id | pubmed-6895598 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-68955982019-12-16 The challenges of translation Salih, Helmut R Jung, Gundram EMBO Mol Med Commentary Cancer immunotherapy is a highly active area in translational medicine where the challenges and rewards of developing new drugs “from bench to bedside” become particularly visible. Here, we comment on both, the scientific and non‐scientific hurdles of this translational process using the example of bispecific antibodies (bsAbs) and chimeric antigen receptor (CAR) T cells, two closely related strategies for antibody‐guided recruitment of T cells against cancer. Both exert impressive therapeutic activity and were recently approved for treatment of B‐cell malignancies. We discuss how the efficacy of these auspicious therapeutic tools may be further improved, in particular against solid tumors, but we also address another critical issue: Since both approaches were already introduced in the 1980s, why did it take almost thirty years until they became clinically available? John Wiley and Sons Inc. 2019-10-18 2019-12 /pmc/articles/PMC6895598/ /pubmed/31625285 http://dx.doi.org/10.15252/emmm.201910874 Text en © 2019 The Authors. Published under the terms of the CC BY 4.0 license This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Commentary Salih, Helmut R Jung, Gundram The challenges of translation |
title | The challenges of translation |
title_full | The challenges of translation |
title_fullStr | The challenges of translation |
title_full_unstemmed | The challenges of translation |
title_short | The challenges of translation |
title_sort | challenges of translation |
topic | Commentary |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6895598/ https://www.ncbi.nlm.nih.gov/pubmed/31625285 http://dx.doi.org/10.15252/emmm.201910874 |
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