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Mesothelin-Targeted Recombinant Immunotoxins for Solid Tumors
Mesothelin (MSLN) is a cell surface glycoprotein normally expressed only on serosal surfaces, and not found in the parenchyma of vital organs. Many solid tumors also express MSLN, including mesothelioma and pancreatic adenocarcinoma. Due to this favorable expression profile, MSLN represents a viable...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7408136/ https://www.ncbi.nlm.nih.gov/pubmed/32605175 http://dx.doi.org/10.3390/biom10070973 |
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author | Hagerty, Brendan L. Pegna, Guillaume J. Xu, Jian Tai, Chin-Hsien Alewine, Christine |
author_facet | Hagerty, Brendan L. Pegna, Guillaume J. Xu, Jian Tai, Chin-Hsien Alewine, Christine |
author_sort | Hagerty, Brendan L. |
collection | PubMed |
description | Mesothelin (MSLN) is a cell surface glycoprotein normally expressed only on serosal surfaces, and not found in the parenchyma of vital organs. Many solid tumors also express MSLN, including mesothelioma and pancreatic adenocarcinoma. Due to this favorable expression profile, MSLN represents a viable target for directed anti-neoplastic therapies, such as recombinant immunotoxins (iToxs). Pre-clinical testing of MSLN-targeted iTox’s has yielded a strong body of evidence for activity against a number of solid tumors. This has led to multiple clinical trials, testing the safety and efficacy of the clinical leads SS1P and LMB-100. While promising clinical results have been observed, neutralizing anti-drug antibody (ADA) formation presents a major challenge to overcome in the therapeutic development process. Additionally, on-target, off-tumor toxicity from serositis and non-specific capillary leak syndrome (CLS) also limits the dose, and therefore, impact anti-tumor activity. This review summarizes existing pre-clinical and clinical data on MSLN-targeted iTox’s. In addition, we address the potential future directions of research to enhance the activity of these anti-tumor agents. |
format | Online Article Text |
id | pubmed-7408136 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-74081362020-08-25 Mesothelin-Targeted Recombinant Immunotoxins for Solid Tumors Hagerty, Brendan L. Pegna, Guillaume J. Xu, Jian Tai, Chin-Hsien Alewine, Christine Biomolecules Review Mesothelin (MSLN) is a cell surface glycoprotein normally expressed only on serosal surfaces, and not found in the parenchyma of vital organs. Many solid tumors also express MSLN, including mesothelioma and pancreatic adenocarcinoma. Due to this favorable expression profile, MSLN represents a viable target for directed anti-neoplastic therapies, such as recombinant immunotoxins (iToxs). Pre-clinical testing of MSLN-targeted iTox’s has yielded a strong body of evidence for activity against a number of solid tumors. This has led to multiple clinical trials, testing the safety and efficacy of the clinical leads SS1P and LMB-100. While promising clinical results have been observed, neutralizing anti-drug antibody (ADA) formation presents a major challenge to overcome in the therapeutic development process. Additionally, on-target, off-tumor toxicity from serositis and non-specific capillary leak syndrome (CLS) also limits the dose, and therefore, impact anti-tumor activity. This review summarizes existing pre-clinical and clinical data on MSLN-targeted iTox’s. In addition, we address the potential future directions of research to enhance the activity of these anti-tumor agents. MDPI 2020-06-28 /pmc/articles/PMC7408136/ /pubmed/32605175 http://dx.doi.org/10.3390/biom10070973 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Hagerty, Brendan L. Pegna, Guillaume J. Xu, Jian Tai, Chin-Hsien Alewine, Christine Mesothelin-Targeted Recombinant Immunotoxins for Solid Tumors |
title | Mesothelin-Targeted Recombinant Immunotoxins for Solid Tumors |
title_full | Mesothelin-Targeted Recombinant Immunotoxins for Solid Tumors |
title_fullStr | Mesothelin-Targeted Recombinant Immunotoxins for Solid Tumors |
title_full_unstemmed | Mesothelin-Targeted Recombinant Immunotoxins for Solid Tumors |
title_short | Mesothelin-Targeted Recombinant Immunotoxins for Solid Tumors |
title_sort | mesothelin-targeted recombinant immunotoxins for solid tumors |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7408136/ https://www.ncbi.nlm.nih.gov/pubmed/32605175 http://dx.doi.org/10.3390/biom10070973 |
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