STAR SIGN study: Evaluation of COVID‐19 vaccine efficacy against the SARS‐CoV‐2 variants BQ.1.1 and XBB.1.5 in patients with inflammatory bowel disease

Author:

Woelfel Simon12ORCID,Dütschler Joel23,König Marius2,Dulovic Alex4,Graf Nicole5,Junker Daniel4,Oikonomou Vasileios6,Krieger Claudia2,Truniger Samuel23,Franke Annett23,Eckhold Annika2,Forsch Kristina2,Koller Seraina2,Wyss Jacqueline6,Krupka Niklas6,Oberholzer Melanie7,Frei Nicola2,Geissler Nora2,Schaub Peter2,Albrich Werner C.8,Friedrich Matthias9,Schneiderhan‐Marra Nicole4,Misselwitz Benjamin6,Korte Wolfgang7,Bürgi Justus J.7,Brand Stephan2ORCID,

Affiliation:

1. Max von Pettenkofer Institute of Hygiene and Medical Microbiology, Faculty of Medicine Ludwig Maximilian University of Munich (LMU Munich) Munich Germany

2. Department of Gastroenterology and Hepatology Cantonal Hospital St. Gallen St. Gallen Switzerland

3. Outpatient Clinic Ambulatory Services Rorschach Rorschach Switzerland

4. NMI Natural and Medical Sciences Institute at the University of Tübingen Reutlingen Germany

5. Clinical Trials Unit Cantonal Hospital St. Gallen St. Gallen Switzerland

6. Department of Visceral Surgery and Medicine Inselspital Bern University Hospital, University of Bern Bern Switzerland

7. Center for Laboratory Medicine St. Gallen Switzerland

8. Division of Infectious Diseases & Hospital Epidemiology Cantonal Hospital St. Gallen St. Gallen Switzerland

9. Translational Gastroenterology Unit, Nuffield Department of Medicine University of Oxford Oxford UK

Abstract

SummaryBackgroundVaccine‐elicited immune responses are impaired in patients with inflammatory bowel disease (IBD) treated with anti‐TNF biologics.AimsTo assess vaccination efficacy against the novel omicron sublineages BQ.1.1 and XBB.1.5 in immunosuppressed patients with IBD.MethodsThis prospective multicentre case–control study included 98 biologic‐treated patients with IBD and 48 healthy controls. Anti‐spike IgG concentrations and surrogate neutralisation against SARS‐CoV‐2 wild‐type, BA.1, BA.5, BQ.1.1, and XBB.1.5 were measured at two different time points (2–16 weeks and 22–40 weeks) following third dose vaccination. Surrogate neutralisation was based on antibody‐mediated blockage of ACE2‐spike protein–protein interaction. Primary outcome was surrogate neutralisation against tested SARS‐CoV‐2 sublineages. Secondary outcomes were proportions of participants with insufficient surrogate neutralisation, impact of breakthrough infection, and correlation of surrogate neutralisation with anti‐spike IgG concentration.ResultsSurrogate neutralisation against all tested sublineages was reduced in patients with IBD who were treated with anti‐TNF biologics compared to patients treated with non‐anti‐TNF biologics and healthy controls (each p ≤ 0.001) at visit 1. Anti‐TNF therapy (odds ratio 0.29 [95% CI 0.19–0.46]) and time since vaccination (0.85 [0.72–1.00]) were associated with low, and mRNA‐1273 vaccination (1.86 [1.12–3.08]) with high wild‐type surrogate neutralisation in a β‐regression model. Accordingly, higher proportions of patients treated with anti‐TNF biologics had insufficient surrogate neutralisation against omicron sublineages at visit 1 compared to patients treated with non‐anti‐TNF biologics and healthy controls (each p ≤ 0.015). Surrogate neutralisation against all tested sublineages decreased over time but was increased by breakthrough infection. Anti‐spike IgG concentrations correlated with surrogate neutralisation.ConclusionsPatients with IBD who are treated with anti‐TNF biologics show impaired neutralisation against novel omicron sublineages BQ.1.1 and XBB.1.5 and may benefit from prioritisation for future variant‐adapted vaccines.

Funder

University of Oxford

Publisher

Wiley

Subject

Pharmacology (medical),Gastroenterology,Hepatology

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