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Tropomyosin autoantibodies associated with checkpoint inhibitor myositis

This brief report details the measurement and identification of IgA antibodies to tropomyosin in a case of presumed ocular myositis with paraspinal myositis in a patient with metastatic uveal melanoma treated with checkpoint inhibitors. High-throughput functional protein microarray analysis and path...

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Detalles Bibliográficos
Autores principales: Zaenker, Pauline, Prentice, David, Ziman, Melanie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7458639/
https://www.ncbi.nlm.nih.gov/pubmed/32923166
http://dx.doi.org/10.1080/2162402X.2020.1804703
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author Zaenker, Pauline
Prentice, David
Ziman, Melanie
author_facet Zaenker, Pauline
Prentice, David
Ziman, Melanie
author_sort Zaenker, Pauline
collection PubMed
description This brief report details the measurement and identification of IgA antibodies to tropomyosin in a case of presumed ocular myositis with paraspinal myositis in a patient with metastatic uveal melanoma treated with checkpoint inhibitors. High-throughput functional protein microarray analysis and pathway analysis was conducted to identify IgG and IgA antibodies of interest. Antibody levels were compared to generic antibody screening results and levels of the antibodies in a cohort of melanoma patients without myositis (n = 100) at baseline prior to undergoing immunotherapy. The finding of specific muscle antibodies in this clinical case indicates the pathogenic potential of anti-tropomyosin IgA in the development of checkpoint inhibitor associated myositis and requires further investigation.
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spelling pubmed-74586392020-09-11 Tropomyosin autoantibodies associated with checkpoint inhibitor myositis Zaenker, Pauline Prentice, David Ziman, Melanie Oncoimmunology Brief Report This brief report details the measurement and identification of IgA antibodies to tropomyosin in a case of presumed ocular myositis with paraspinal myositis in a patient with metastatic uveal melanoma treated with checkpoint inhibitors. High-throughput functional protein microarray analysis and pathway analysis was conducted to identify IgG and IgA antibodies of interest. Antibody levels were compared to generic antibody screening results and levels of the antibodies in a cohort of melanoma patients without myositis (n = 100) at baseline prior to undergoing immunotherapy. The finding of specific muscle antibodies in this clinical case indicates the pathogenic potential of anti-tropomyosin IgA in the development of checkpoint inhibitor associated myositis and requires further investigation. Taylor & Francis 2020-08-12 /pmc/articles/PMC7458639/ /pubmed/32923166 http://dx.doi.org/10.1080/2162402X.2020.1804703 Text en © 2020 The Author(s). Published with license by Taylor & Francis Group, LLC. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Brief Report
Zaenker, Pauline
Prentice, David
Ziman, Melanie
Tropomyosin autoantibodies associated with checkpoint inhibitor myositis
title Tropomyosin autoantibodies associated with checkpoint inhibitor myositis
title_full Tropomyosin autoantibodies associated with checkpoint inhibitor myositis
title_fullStr Tropomyosin autoantibodies associated with checkpoint inhibitor myositis
title_full_unstemmed Tropomyosin autoantibodies associated with checkpoint inhibitor myositis
title_short Tropomyosin autoantibodies associated with checkpoint inhibitor myositis
title_sort tropomyosin autoantibodies associated with checkpoint inhibitor myositis
topic Brief Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7458639/
https://www.ncbi.nlm.nih.gov/pubmed/32923166
http://dx.doi.org/10.1080/2162402X.2020.1804703
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