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Smaller size packs a stronger punch - Recent advances in small antibody fragments targeting tumour-associated carbohydrate antigens
Attached to proteins, lipids, or forming long, complex chains, glycans represent the most versatile post-translational modification in nature and surround all human cells. Unique glycan structures are monitored by the immune system and differentiate self from non-self and healthy from malignant cell...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Ivyspring International Publisher
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10240822/ https://www.ncbi.nlm.nih.gov/pubmed/37284439 http://dx.doi.org/10.7150/thno.80901 |
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author | Khilji, Sana Khan Op 't Hoog, Charlotte Warschkau, David Lühle, Jost Goerdeler, Felix Freitag, Anika Seeberger, Peter H. Moscovitz, Oren |
author_facet | Khilji, Sana Khan Op 't Hoog, Charlotte Warschkau, David Lühle, Jost Goerdeler, Felix Freitag, Anika Seeberger, Peter H. Moscovitz, Oren |
author_sort | Khilji, Sana Khan |
collection | PubMed |
description | Attached to proteins, lipids, or forming long, complex chains, glycans represent the most versatile post-translational modification in nature and surround all human cells. Unique glycan structures are monitored by the immune system and differentiate self from non-self and healthy from malignant cells. Aberrant glycosylations, termed tumour-associated carbohydrate antigens (TACAs), are a hallmark of cancer and are correlated with all aspects of cancer biology. Therefore, TACAs represent attractive targets for monoclonal antibodies for cancer diagnosis and therapy. However, due to the thick and dense glycocalyx as well as the tumour micro-environment, conventional antibodies often suffer from restricted access and limited effectiveness in vivo. To overcome this issue, many small antibody fragments have come forth, showing similar affinity with better efficiency than their full-length counterparts. Here we review small antibody fragments against specific glycans on tumour cells and highlight their advantages over conventional antibodies. |
format | Online Article Text |
id | pubmed-10240822 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Ivyspring International Publisher |
record_format | MEDLINE/PubMed |
spelling | pubmed-102408222023-06-06 Smaller size packs a stronger punch - Recent advances in small antibody fragments targeting tumour-associated carbohydrate antigens Khilji, Sana Khan Op 't Hoog, Charlotte Warschkau, David Lühle, Jost Goerdeler, Felix Freitag, Anika Seeberger, Peter H. Moscovitz, Oren Theranostics Review Attached to proteins, lipids, or forming long, complex chains, glycans represent the most versatile post-translational modification in nature and surround all human cells. Unique glycan structures are monitored by the immune system and differentiate self from non-self and healthy from malignant cells. Aberrant glycosylations, termed tumour-associated carbohydrate antigens (TACAs), are a hallmark of cancer and are correlated with all aspects of cancer biology. Therefore, TACAs represent attractive targets for monoclonal antibodies for cancer diagnosis and therapy. However, due to the thick and dense glycocalyx as well as the tumour micro-environment, conventional antibodies often suffer from restricted access and limited effectiveness in vivo. To overcome this issue, many small antibody fragments have come forth, showing similar affinity with better efficiency than their full-length counterparts. Here we review small antibody fragments against specific glycans on tumour cells and highlight their advantages over conventional antibodies. Ivyspring International Publisher 2023-05-15 /pmc/articles/PMC10240822/ /pubmed/37284439 http://dx.doi.org/10.7150/thno.80901 Text en © The author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions. |
spellingShingle | Review Khilji, Sana Khan Op 't Hoog, Charlotte Warschkau, David Lühle, Jost Goerdeler, Felix Freitag, Anika Seeberger, Peter H. Moscovitz, Oren Smaller size packs a stronger punch - Recent advances in small antibody fragments targeting tumour-associated carbohydrate antigens |
title | Smaller size packs a stronger punch - Recent advances in small antibody fragments targeting tumour-associated carbohydrate antigens |
title_full | Smaller size packs a stronger punch - Recent advances in small antibody fragments targeting tumour-associated carbohydrate antigens |
title_fullStr | Smaller size packs a stronger punch - Recent advances in small antibody fragments targeting tumour-associated carbohydrate antigens |
title_full_unstemmed | Smaller size packs a stronger punch - Recent advances in small antibody fragments targeting tumour-associated carbohydrate antigens |
title_short | Smaller size packs a stronger punch - Recent advances in small antibody fragments targeting tumour-associated carbohydrate antigens |
title_sort | smaller size packs a stronger punch - recent advances in small antibody fragments targeting tumour-associated carbohydrate antigens |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10240822/ https://www.ncbi.nlm.nih.gov/pubmed/37284439 http://dx.doi.org/10.7150/thno.80901 |
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