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Antibody Diversity in Cancer: Translational Implications and Beyond
Patients with cancer tend to develop antibodies to autologous proteins. This phenomenon has been observed across multiple cancer types, including bladder, lung, colon, prostate, and melanoma. These antibodies potentially arise due to induced inflammation or an increase in self-antigens. Studies focu...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9331493/ https://www.ncbi.nlm.nih.gov/pubmed/35893814 http://dx.doi.org/10.3390/vaccines10081165 |
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author | Reddy, Raghuram Mintz, Joel Golan, Roei Firdaus, Fakiha Ponce, Roxana Van Booven, Derek Manoharan, Aysswarya Issa, Isabelle Blomberg, Bonnie B. Arora, Himanshu |
author_facet | Reddy, Raghuram Mintz, Joel Golan, Roei Firdaus, Fakiha Ponce, Roxana Van Booven, Derek Manoharan, Aysswarya Issa, Isabelle Blomberg, Bonnie B. Arora, Himanshu |
author_sort | Reddy, Raghuram |
collection | PubMed |
description | Patients with cancer tend to develop antibodies to autologous proteins. This phenomenon has been observed across multiple cancer types, including bladder, lung, colon, prostate, and melanoma. These antibodies potentially arise due to induced inflammation or an increase in self-antigens. Studies focusing on antibody diversity are particularly attractive for their diagnostic value considering antibodies are present at an early diseased stage, serum samples are relatively easy to obtain, and the prevalence of antibodies is high even when the target antigen is minimally expressed. Conversely, the surveillance of serum proteins in cancer patients is relatively challenging because they often show variability in expression and are less abundant. Moreover, an antibody’s presence is also useful as it suggests the relative immunogenicity of a given antigen. For these reasons, profiling antibodies’ responses is actively considered to detect the spread of antigens following immunotherapy. The current review focuses on expanding the knowledge of antibodies and their diversity, and the impact of antibody diversity on cancer regression and progression. |
format | Online Article Text |
id | pubmed-9331493 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-93314932022-07-29 Antibody Diversity in Cancer: Translational Implications and Beyond Reddy, Raghuram Mintz, Joel Golan, Roei Firdaus, Fakiha Ponce, Roxana Van Booven, Derek Manoharan, Aysswarya Issa, Isabelle Blomberg, Bonnie B. Arora, Himanshu Vaccines (Basel) Review Patients with cancer tend to develop antibodies to autologous proteins. This phenomenon has been observed across multiple cancer types, including bladder, lung, colon, prostate, and melanoma. These antibodies potentially arise due to induced inflammation or an increase in self-antigens. Studies focusing on antibody diversity are particularly attractive for their diagnostic value considering antibodies are present at an early diseased stage, serum samples are relatively easy to obtain, and the prevalence of antibodies is high even when the target antigen is minimally expressed. Conversely, the surveillance of serum proteins in cancer patients is relatively challenging because they often show variability in expression and are less abundant. Moreover, an antibody’s presence is also useful as it suggests the relative immunogenicity of a given antigen. For these reasons, profiling antibodies’ responses is actively considered to detect the spread of antigens following immunotherapy. The current review focuses on expanding the knowledge of antibodies and their diversity, and the impact of antibody diversity on cancer regression and progression. MDPI 2022-07-22 /pmc/articles/PMC9331493/ /pubmed/35893814 http://dx.doi.org/10.3390/vaccines10081165 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Reddy, Raghuram Mintz, Joel Golan, Roei Firdaus, Fakiha Ponce, Roxana Van Booven, Derek Manoharan, Aysswarya Issa, Isabelle Blomberg, Bonnie B. Arora, Himanshu Antibody Diversity in Cancer: Translational Implications and Beyond |
title | Antibody Diversity in Cancer: Translational Implications and Beyond |
title_full | Antibody Diversity in Cancer: Translational Implications and Beyond |
title_fullStr | Antibody Diversity in Cancer: Translational Implications and Beyond |
title_full_unstemmed | Antibody Diversity in Cancer: Translational Implications and Beyond |
title_short | Antibody Diversity in Cancer: Translational Implications and Beyond |
title_sort | antibody diversity in cancer: translational implications and beyond |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9331493/ https://www.ncbi.nlm.nih.gov/pubmed/35893814 http://dx.doi.org/10.3390/vaccines10081165 |
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