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Adalimumab and Infliximab Impair SARS-CoV-2 Antibody Responses: Results from a Therapeutic Drug Monitoring Study in 11 422 Biologic-Treated Patients

  • Neil Chanchlani
  • , Simeng Lin
  • , Desmond Chee
  • , Benjamin Hamilton
  • , Rachel Nice
  • , Zehra Arkir
  • , Claire Bewshea
  • , Bessie Cipriano
  • , Lauranne A.A.P. Derikx
  • , Allan Dunlop
  • , Louise Greathead
  • , Rachel L. Griffiths
  • , Hajir Ibraheim
  • , Peter Kelleher
  • , Klaartje B. Kok
  • , Charlie W. Lees
  • , Jonathan MacDonald
  • , Shaji Sebastian
  • , Philip J. Smith
  • , Timothy J. McDonald
  • Peter M. Irving, Nick Powell, Nicholas A. Kennedy, James R. Goodhand, Tariq Ahmad*
*Corresponding author for this work
  • Royal Devon & Exeter NHS Foundation Trust
  • University of Exeter
  • Guy's and St Thomas' NHS Foundation Trust
  • Barts Health NHS Trust
  • Western General Hospital (Edinburgh)
  • Queen Elizabeth University Hospital (Birmingham)
  • North West London Pathology
  • Sandwell and West Birmingham Hospitals NHS Trust
  • Imperial College London
  • Queen Mary University of London
  • University of Edinburgh
  • University of Glasgow
  • Hull University Teaching Hospitals NHS Trust
  • University of Hull
  • Liverpool University Hospitals NHS Foundation Trust
  • King's College London

Research output: Contribution to journalArticleAcademicpeer-review

40 Citations (Scopus)

Abstract

Background and Aims: Infliximab attenuates serological responses to SARS-CoV-2 infection. Whether this is a class effect, or if anti-tumour necrosis factor [anti-TNF] level influences serological responses, remains unknown. Methods: Seroprevalence and the magnitude of SARS-CoV-2 nucleocapsid antibody responses were measured in surplus serum from 11 422 (53.3% [6084] male; median age 36.8 years) patients with immune-mediated inflammatory diseases, stored at six therapeutic drug monitoring laboratories between January 29 and September 30, 2020. Data were linked to nationally held SARS-CoV-2 PCR results to July 11, 2021. Results: Rates of PCR-confirmed SARS-CoV-2 infection were similar across treatment groups. Seroprevalence rates were lower in infliximab- and adalimumab- than vedolizumab-treated patients (infliximab: 3.0% [178/5893], adalimumab: 3.0% [152/5074], vedolizumab: 6.7% [25/375], p = 0.003). The magnitude of SARS-CoV-2 reactivity was similar in infliximab- vs adalimumab-treated patients (median 4.30 cut-off index [COI] [1.94-9.96] vs 5.02 [2.18-18.70], p = 0.164), but higher in vedolizumab-treated patients (median 21.60 COI [4.39-68.10, p < 0.004). Compared to patients with detectable infliximab and adalimumab drug levels, patients with undetectable drug levels [<0.8 mg/L] were more likely to be seropositive for SARS-CoV-2 antibodies. One-third of patients who had PCR testing prior to antibody testing failed to seroconvert, all were treated with anti-TNF. Subsequent positive PCR-confirmed SARS-CoV-2 was seen in 7.9% [12/152] of patients after a median time of 183.5 days [129.8-235.3], without differences between drugs. Conclusion: Anti-TNF treatment is associated with lower SARS-CoV-2 nucleocapsid seroprevalence and antibody reactivity when compared to vedolizumab-treated patients. Higher seropositivity rates in patients with undetectable anti-TNF levels support a causal relationship, although confounding factors, such as combination therapy with a immunomodulator, may have influenced the results.

Original languageEnglish
Pages (from-to)389-397
Number of pages9
JournalJournal of Crohn's and Colitis
Volume16
Issue number3
DOIs
Publication statusPublished - 1 Mar 2022
Externally publishedYes

Bibliographical note

Publisher Copyright:
© 2021 The Author(s).

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