The challenges of translation

Abstract 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 ex...

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Main Authors: Helmut R Salih, Gundram Jung
Format: Article
Language:English
Published: Springer Nature 2019-10-01
Series:EMBO Molecular Medicine
Online Access:https://doi.org/10.15252/emmm.201910874
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author Helmut R Salih
Gundram Jung
author_facet Helmut R Salih
Gundram Jung
author_sort Helmut R Salih
collection DOAJ
description Abstract 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?
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spelling doaj-art-0dde4d3e2d5b43839b4a942320891a2e2025-08-20T03:43:10ZengSpringer NatureEMBO Molecular Medicine1757-46761757-46842019-10-0111121310.15252/emmm.201910874The challenges of translationHelmut R Salih0Gundram Jung1Clinical Collaboration Unit Translational Immunology, German Cancer Consortium (DKTK), Department of Internal Medicine, University of TübingenDepartment of Immunology, Institute for Cell Biology, University of TübingenAbstract 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?https://doi.org/10.15252/emmm.201910874
spellingShingle Helmut R Salih
Gundram Jung
The challenges of translation
EMBO Molecular Medicine
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
url https://doi.org/10.15252/emmm.201910874
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