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

Author:

Chanchlani Neil12ORCID,Lin Simeng12ORCID,Chee Desmond12ORCID,Hamilton Benjamin12,Nice Rachel3,Arkir Zehra4ORCID,Bewshea Claire2ORCID,Cipriano Bessie5,Derikx Lauranne A A P67ORCID,Dunlop Allan8,Greathead Louise9ORCID,Griffiths Rachel L10,Ibraheim Hajir1112ORCID,Kelleher Peter913,Kok Klaartje B514ORCID,Lees Charlie W615ORCID,MacDonald Jonathan1617ORCID,Sebastian Shaji1819ORCID,Smith Philip J20ORCID,McDonald Timothy J3ORCID,Irving Peter M2122ORCID,Powell Nick1112ORCID,Kennedy Nicholas A12ORCID,Goodhand James R12ORCID,Ahmad Tariq12ORCID

Affiliation:

1. Gastroenterology, Royal Devon and Exeter NHS Foundation Trust, Exeter, UK

2. Exeter Inflammatory Bowel Disease and Pharmacogenetics Research Group, University of Exeter, Exeter, UK

3. Biochemistry, Exeter Clinical Laboratory International, Royal Devon and Exeter NHS Foundation Trust, Exeter, UK

4. Viapath Analytics, Guy’s and St Thomas’ NHS Foundation Trust, London, UK

5. Gastroenterology, Barts and The London NHS Trust, London, UK

6. Gastroenterology, Western General Hospital, NHS Lothian, Edinburgh, UK

7. Gastroenterology and Hepatology, Inflammatory Bowel Disease Center, Radboud University Medical Center, Nijmegen, the Netherlands

8. Biochemistry, Queen Elizabeth University Hospital, NHS Greater Glasgow and Clyde, Glasgow, UK

9. Infection & Immunity Sciences, North West London Pathology, London, UK

10. Biochemistry, Sandwell & West Birmingham NHS Trust, Birmingham, UK

11. Metabolism, Digestion and Reproduction, Imperial College London, London, UK

12. Gastroenterology, Imperial College Healthcare NHS Trust, London, UK

13. Infectious Diseases, Imperial College Healthcare NHS Trust, London, UK

14. Centre for Immunobiology, Blizard Institute, Barts and The London School of Medicine and Dentistry Blizard Institute, London, UK

15. Institute of Genetic and Molecular Medicine, University of Edinburgh, Edinburgh, UK

16. Gastroenterology, Queen Elizabeth University Hospital, NHS Greater Glasgow and Clyde, Glasgow, UK

17. School of Medicine, Dentistry and Nursing, University of Glasgow, Glasgow, UK

18. IBD Unit – Gastroenterology, Hull University Teaching Hospitals NHS Trust, Hull, UK

19. Hull York Medical School, University of Hull, Hull, UK

20. Gastroenterology, Liverpool University Hospitals NHS Foundation Trust, Liverpool, UK

21. Gastroenterology, Guy’s and St Thomas’ Hospitals NHS Trust, London, UK

22. School of Immunology & Microbial Sciences, King’s College London, London, UK

Abstract

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.

Publisher

Oxford University Press (OUP)

Subject

Gastroenterology,General Medicine

Reference31 articles.

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