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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

Simeng Lin

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

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

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