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Journal article

The impact of CGRP monoclonal antibodies on cytokine expression in chronic migraine: a cohort study

Abstract:

Background

Calcitonin gene-related peptide monoclonal antibodies (CGRP mAbs) are an effective preventative therapy for migraine; however, there have been rare reports of possible inflammatory complications. The primary objective of this study was to examine the impact of CGRP mAbs on immune system activation by evaluating the plasma cytokine profile of a cohort of patients pre- and post-CGRP mAb.

Methodology

A prospective cohort study was undertaken at a tertiary headache service. Following informed consent and screening, the plasma cytokine profile of participants was determined using a Simoa CorPlex human cytokine 10-plex with ten targets: interferon gamma, interleukin-1β, IL-4, IL-5, IL-6, IL-8, IL-10, IL-12p70, IL-22, and TNF⍺ prior to initiation of CGRP mAb and following 3 months of therapy. A comparator group of healthy controls at a single time point was also included.

Results

A total of 22 patients with chronic migraine and 10 healthy controls were included in the study. Administration of CGRP mAb was not associated with a significant change in cytokine expression (Wilk's lambda 0.528, p = 0.448). On post-hoc analysis, there was a significant reduction in IL-5 levels (z = - 2.321, p = 0.020) following CGRP mAb therapy.

Conclusion

In this study of patients with chronic migraine, we found no evidence that treatment with CGRP mABs is associated with a significant alteration in plasma cytokine levels or shift to a Th1 phenotype.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1007/s00415-025-13400-w

Authors

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Role:
Author
ORCID:
0000-0003-4833-5507
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Role:
Author
ORCID:
0000-0001-5190-3179
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Role:
Author
ORCID:
0000-0003-0190-5760
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Institution:
University of Oxford
Role:
Author
ORCID:
0000-0002-5335-6612


Publisher:
Springer
Journal:
Journal of Neurology More from this journal
Volume:
272
Issue:
10
Pages:
649-649
Publication date:
2025-09-24
DOI:
EISSN:
1432-1459
ISSN:
0340-5354


Language:
English
Pubs id:
2344417
Local pid:
pubs:2344417
Source identifiers:
W4414450710
Deposit date:
2025-12-04
ARK identifier:
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