Simeng Lin
Antibody decay, T cell immunity and breakthrough infections following two SARS-CoV-2 vaccine doses in inflammatory bowel disease patients treated with infliximab and vedolizumab
Lin, Simeng; Kennedy, Nicholas A.; Saifuddin, Aamir; Sandoval, Diana Muñoz; Reynolds, Catherine J.; Castro Seoane, Rocio; Kottoor, Sherine H.; Pieper, Franziska P.; Lin, Kai-Min; Butler, David K.; Chanchlani, Neil; Nice, Rachel; Chee, Desmond; Bewshea, Claire; Janjua, Malik; Mcdonald, Timothy J.; Sebastian, Shaji; Alexander, James L.; Constable, Laura; Lee, James C.; Murray, Charles D.; Hart, Alisa L.; Irving, Peter M.; Jones, Gareth-Rhys
Authors
Nicholas A. Kennedy
Aamir Saifuddin
Diana Muñoz Sandoval
Catherine J. Reynolds
Rocio Castro Seoane
Sherine H. Kottoor
Franziska P. Pieper
Kai-Min Lin
David K. Butler
Neil Chanchlani
Rachel Nice
Desmond Chee
Claire Bewshea
Malik Janjua
Timothy J. Mcdonald
Shaji Sebastian
James L. Alexander
Laura Constable
James C. Lee
Charles D. Murray
Alisa L. Hart
Peter M. Irving
Gareth-Rhys Jones
Contributors
GORDON MORAN GORDON.MORAN@NOTTINGHAM.AC.UK
Researcher
Abstract
Anti tumour necrosis factor (anti-TNF) drugs increase the risk of serious respiratory infection and impair protective immunity following pneumococcal and influenza vaccination. Here we report SARS-CoV-2 vaccine-induced immune responses and breakthrough infections in patients with inflammatory bowel disease, who are treated either with the anti-TNF antibody, infliximab, or with vedolizumab targeting a gut-specific anti-integrin that does not impair systemic immunity. Geometric mean [SD] anti-S RBD antibody concentrations are lower and half-lives shorter in patients treated with infliximab than vedolizumab, following two doses of BNT162b2 (566.7 U/mL [6.2] vs 4555.3 U/mL [5.4], p <0.0001; 26.8 days [95% CI 26.2-27.5] vs 47.6 days [45.5-49.8], p <0.0001); similar results are also observed with ChAdOx1 nCoV-19 vaccination (184.7 U/mL [5.0] vs 784.0 U/mL [3.5], p <0.0001; 35.9 days [34.9-36.8] vs 58.0 days [55.0-61.3], p value < 0.0001). One fifth of patients fail to mount a T cell response in both treatment groups. Breakthrough SARS-CoV-2 infections are more frequent (5.8% (201/3441) vs 3.9% (66/1682), p = 0.0039) in patients treated with infliximab than vedolizumab, and the risk of breakthrough SARS-CoV-2 infection is predicted by peak anti-S RBD antibody concentration after two vaccine doses. Irrespective of the treatments, higher, more sustained antibody levels are observed in patients with a history of SARS-CoV-2 infection prior to vaccination. Our results thus suggest that adapted vaccination schedules may be required to induce immunity in at-risk, anti-TNF-treated patients.
Citation
Lin, S., Kennedy, N. A., Saifuddin, A., Sandoval, D. M., Reynolds, C. J., Castro Seoane, R., …Jones, G. (2022). Antibody decay, T cell immunity and breakthrough infections following two SARS-CoV-2 vaccine doses in inflammatory bowel disease patients treated with infliximab and vedolizumab. Nature Communications, 13, Article 1379. https://doi.org/10.1038/s41467-022-28517-z
Journal Article Type | Article |
---|---|
Acceptance Date | Jan 26, 2022 |
Online Publication Date | Mar 16, 2022 |
Publication Date | Mar 16, 2022 |
Deposit Date | Oct 30, 2023 |
Publicly Available Date | Nov 10, 2023 |
Journal | Nature Communications |
Electronic ISSN | 2041-1723 |
Publisher | Nature Publishing Group |
Peer Reviewed | Peer Reviewed |
Volume | 13 |
Article Number | 1379 |
DOI | https://doi.org/10.1038/s41467-022-28517-z |
Public URL | https://nottingham-repository.worktribe.com/output/26797230 |
Publisher URL | https://www.nature.com/articles/s41467-022-28517-z |
Files
41467 2022 Article 28517
(2.6 Mb)
PDF
Publisher Licence URL
https://creativecommons.org/licenses/by/4.0/
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