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Case report: Granzyme-B expression by T- and B- cells during severe AQP4-positive Neuromyelitis Optica spectrum disorder with fatal venous thromboembolism outcome
BACKGROUND: The expression of serine protease granzyme-B (GzmB) by circulating CD8(+) T lymphocytes has been recently suggested as a biomarker for poor immunotherapy response and severe disability in patients with Neuromyelitis Optica spectrum disorders (NMOSD). In parallel, venous thromboembolism (...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10470460/ https://www.ncbi.nlm.nih.gov/pubmed/37662034 http://dx.doi.org/10.3389/fneur.2023.1208977 |
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author | Boldrini, Vinícius Oliveira Brito, Mariana Rabelo Quintiliano, Raphael Patrício Silva Scárdua Silva, Lucas Yasuda, Clarissa Lin Cendes, Fernando Farias, Alessandro Santos Damasceno, Alfredo |
author_facet | Boldrini, Vinícius Oliveira Brito, Mariana Rabelo Quintiliano, Raphael Patrício Silva Scárdua Silva, Lucas Yasuda, Clarissa Lin Cendes, Fernando Farias, Alessandro Santos Damasceno, Alfredo |
author_sort | Boldrini, Vinícius Oliveira |
collection | PubMed |
description | BACKGROUND: The expression of serine protease granzyme-B (GzmB) by circulating CD8(+) T lymphocytes has been recently suggested as a biomarker for poor immunotherapy response and severe disability in patients with Neuromyelitis Optica spectrum disorders (NMOSD). In parallel, venous thromboembolism (VTE) has been reported mainly in NMOSD patients exhibiting transverse myelitis. CASE PRESENTATION: Here, we describe an Aquaporin-4 positive (AQP4-positive) NMOSD patient who showed short myelitis (SM) and experienced a fatal pulmonary thromboembolism/lower extremity deep vein thrombosis during anti-CD20 treatment. Flow cytometry analyses from the peripheral blood revealed an enhanced cytotoxic behavior through circulating CD8(+)GzmB(+) T, CD4(+)GzmB(+) T lymphocytes, and residual CD19(+)GzmB(+) B cells. CONCLUSIONS: Fatal VTE may be a rare outcome, particularly in patients exhibiting SM, and may share poorly understood immunological mechanisms with AQP4-positive NMOSD severity. |
format | Online Article Text |
id | pubmed-10470460 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-104704602023-09-01 Case report: Granzyme-B expression by T- and B- cells during severe AQP4-positive Neuromyelitis Optica spectrum disorder with fatal venous thromboembolism outcome Boldrini, Vinícius Oliveira Brito, Mariana Rabelo Quintiliano, Raphael Patrício Silva Scárdua Silva, Lucas Yasuda, Clarissa Lin Cendes, Fernando Farias, Alessandro Santos Damasceno, Alfredo Front Neurol Neurology BACKGROUND: The expression of serine protease granzyme-B (GzmB) by circulating CD8(+) T lymphocytes has been recently suggested as a biomarker for poor immunotherapy response and severe disability in patients with Neuromyelitis Optica spectrum disorders (NMOSD). In parallel, venous thromboembolism (VTE) has been reported mainly in NMOSD patients exhibiting transverse myelitis. CASE PRESENTATION: Here, we describe an Aquaporin-4 positive (AQP4-positive) NMOSD patient who showed short myelitis (SM) and experienced a fatal pulmonary thromboembolism/lower extremity deep vein thrombosis during anti-CD20 treatment. Flow cytometry analyses from the peripheral blood revealed an enhanced cytotoxic behavior through circulating CD8(+)GzmB(+) T, CD4(+)GzmB(+) T lymphocytes, and residual CD19(+)GzmB(+) B cells. CONCLUSIONS: Fatal VTE may be a rare outcome, particularly in patients exhibiting SM, and may share poorly understood immunological mechanisms with AQP4-positive NMOSD severity. Frontiers Media S.A. 2023-08-17 /pmc/articles/PMC10470460/ /pubmed/37662034 http://dx.doi.org/10.3389/fneur.2023.1208977 Text en Copyright © 2023 Boldrini, Brito, Quintiliano, Scárdua Silva, Yasuda, Cendes, Farias and Damasceno. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neurology Boldrini, Vinícius Oliveira Brito, Mariana Rabelo Quintiliano, Raphael Patrício Silva Scárdua Silva, Lucas Yasuda, Clarissa Lin Cendes, Fernando Farias, Alessandro Santos Damasceno, Alfredo Case report: Granzyme-B expression by T- and B- cells during severe AQP4-positive Neuromyelitis Optica spectrum disorder with fatal venous thromboembolism outcome |
title | Case report: Granzyme-B expression by T- and B- cells during severe AQP4-positive Neuromyelitis Optica spectrum disorder with fatal venous thromboembolism outcome |
title_full | Case report: Granzyme-B expression by T- and B- cells during severe AQP4-positive Neuromyelitis Optica spectrum disorder with fatal venous thromboembolism outcome |
title_fullStr | Case report: Granzyme-B expression by T- and B- cells during severe AQP4-positive Neuromyelitis Optica spectrum disorder with fatal venous thromboembolism outcome |
title_full_unstemmed | Case report: Granzyme-B expression by T- and B- cells during severe AQP4-positive Neuromyelitis Optica spectrum disorder with fatal venous thromboembolism outcome |
title_short | Case report: Granzyme-B expression by T- and B- cells during severe AQP4-positive Neuromyelitis Optica spectrum disorder with fatal venous thromboembolism outcome |
title_sort | case report: granzyme-b expression by t- and b- cells during severe aqp4-positive neuromyelitis optica spectrum disorder with fatal venous thromboembolism outcome |
topic | Neurology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10470460/ https://www.ncbi.nlm.nih.gov/pubmed/37662034 http://dx.doi.org/10.3389/fneur.2023.1208977 |
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