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Inflammatory complications of CGRP monoclonal antibodies: a case series
BACKGROUND: Calcitonin gene-related peptide (CGRP) is expressed throughout the body and is a known mediator of migraine, exerting this biological effect through activation of trigeminovascular, meningeal and associated neuronal pathways located in close proximity to the central nervous system. Monoc...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Milan
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8501661/ https://www.ncbi.nlm.nih.gov/pubmed/34625019 http://dx.doi.org/10.1186/s10194-021-01330-7 |
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author | Ray, Jason C. Allen, Penelope Bacsi, Ann Bosco, Julian J. Chen, Luke Eller, Michael Kua, Hock Lim, Lyndell L. Matharu, Manjit S. Monif, Mastura Ruttledge, Martin Stark, Richard J. Hutton, Elspeth J. |
author_facet | Ray, Jason C. Allen, Penelope Bacsi, Ann Bosco, Julian J. Chen, Luke Eller, Michael Kua, Hock Lim, Lyndell L. Matharu, Manjit S. Monif, Mastura Ruttledge, Martin Stark, Richard J. Hutton, Elspeth J. |
author_sort | Ray, Jason C. |
collection | PubMed |
description | BACKGROUND: Calcitonin gene-related peptide (CGRP) is expressed throughout the body and is a known mediator of migraine, exerting this biological effect through activation of trigeminovascular, meningeal and associated neuronal pathways located in close proximity to the central nervous system. Monoclonal antibodies (mAb) targeting the CGRP pathway are an effective new preventive treatment for migraine, with a generally favourable adverse event profile. Pre-clinical evidence supports an anti-inflammatory/immunoregulatory role for CGRP in other organ systems, and therefore inhibition of the normal action of this peptide may promote a pro-inflammatory response. CASES: We present a case series of eight patients with new or significantly worsened inflammatory pathology in close temporal association with the commencement of CGRP mAb therapy. CONCLUSION: This case series provides novel insights on the potential molecular mechanisms and side-effects of CGRP antagonism in migraine and supports clinical vigilance in patient care going forward. |
format | Online Article Text |
id | pubmed-8501661 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer Milan |
record_format | MEDLINE/PubMed |
spelling | pubmed-85016612021-10-20 Inflammatory complications of CGRP monoclonal antibodies: a case series Ray, Jason C. Allen, Penelope Bacsi, Ann Bosco, Julian J. Chen, Luke Eller, Michael Kua, Hock Lim, Lyndell L. Matharu, Manjit S. Monif, Mastura Ruttledge, Martin Stark, Richard J. Hutton, Elspeth J. J Headache Pain Case Report BACKGROUND: Calcitonin gene-related peptide (CGRP) is expressed throughout the body and is a known mediator of migraine, exerting this biological effect through activation of trigeminovascular, meningeal and associated neuronal pathways located in close proximity to the central nervous system. Monoclonal antibodies (mAb) targeting the CGRP pathway are an effective new preventive treatment for migraine, with a generally favourable adverse event profile. Pre-clinical evidence supports an anti-inflammatory/immunoregulatory role for CGRP in other organ systems, and therefore inhibition of the normal action of this peptide may promote a pro-inflammatory response. CASES: We present a case series of eight patients with new or significantly worsened inflammatory pathology in close temporal association with the commencement of CGRP mAb therapy. CONCLUSION: This case series provides novel insights on the potential molecular mechanisms and side-effects of CGRP antagonism in migraine and supports clinical vigilance in patient care going forward. Springer Milan 2021-10-09 /pmc/articles/PMC8501661/ /pubmed/34625019 http://dx.doi.org/10.1186/s10194-021-01330-7 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Case Report Ray, Jason C. Allen, Penelope Bacsi, Ann Bosco, Julian J. Chen, Luke Eller, Michael Kua, Hock Lim, Lyndell L. Matharu, Manjit S. Monif, Mastura Ruttledge, Martin Stark, Richard J. Hutton, Elspeth J. Inflammatory complications of CGRP monoclonal antibodies: a case series |
title | Inflammatory complications of CGRP monoclonal antibodies: a case series |
title_full | Inflammatory complications of CGRP monoclonal antibodies: a case series |
title_fullStr | Inflammatory complications of CGRP monoclonal antibodies: a case series |
title_full_unstemmed | Inflammatory complications of CGRP monoclonal antibodies: a case series |
title_short | Inflammatory complications of CGRP monoclonal antibodies: a case series |
title_sort | inflammatory complications of cgrp monoclonal antibodies: a case series |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8501661/ https://www.ncbi.nlm.nih.gov/pubmed/34625019 http://dx.doi.org/10.1186/s10194-021-01330-7 |
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