Nationwide experiences with trough levels, durability, and disease activity among inflammatory bowel disease patients following COVID-19 vaccination

Author:

Resál Tamás1ORCID,Bacsur Péter1ORCID,Horváth Miklós2,Szántó Kata1ORCID,Rutka Mariann1,Bálint Anita1,Fábián Anna1ORCID,Bor Renáta1ORCID,Szepes Zoltán1,Fekete János3,Farkas Klaudia1,Miheller Pál2,Molnár Tamás4

Affiliation:

1. Department of Medicine, Albert Szent-Györgyi Medical School, University of Szeged, Szeged, Hungary

2. Department of Surgery and Interventional Gastroenterology, Faculty of Medicine, Semmelweis University, Budapest, Hungary

3. Department of Bioinformatics, Semmelweis University, Budapest, Hungary

4. Department of Medicine, Albert Szent-Györgyi Medical School, University of Szeged, Kálvária Avenue 57, Szeged, H-6720, Hungary

Abstract

Background: The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic has complicated the management of inflammatory bowel diseases (IBD). Objectives: This study aimed to assess the efficacy of different anti-SARS-CoV-2 vaccines under different treatments in IBD patients and identify predictive factors associated with lower serological response, including anti-tumor necrosis factor (anti-TNF) drug levels. Design: A prospective, double-center study of IBD patients was conducted following messenger ribonucleotide acid (mRNA) and non-mRNA anti-SARS-CoV-2 vaccination. Methods: Healthy control (HC) patients were enrolled to reduce bias. Baseline and control samples were obtained 14 days after the second dose to assess the impact of conventional and biological treatments. Clinical and biochemical activity, serological response level, and anti-TNF drug levels were measured. Results: This study included 199 IBD (mean age, 40.9 ± 12.72 years) and 77 HC participants (mean age, 50.3 ± 12.36 years). Most patients (76.9%) and all HCs received mRNA vaccines. Half of the IBD patients were on biological treatment (anti-TNF 68.7%). Biological and thiopurine combined immunomodulation and biological treatment were associated with lower serological response ( p < 0.001), and mRNA vaccination promoted better antibody levels ( p < 0.001). Higher adalimumab levels caused lower serological response ( p = 0.006). W8 persistence of anti-SARS-CoV-2 level was equal in IBD and HC groups. Vaccination did not aggravate clinical disease activity ( p = 0.65). Conclusion: Anti-SARS-CoV-2 vaccination is considerably efficacious in IBD patients, with mRNA vaccines promoting better antibody levels. The negative impact of combined biological treatment, especially with high adalimumab drug levels, on serological response to vaccination should be considered. Although midterm durability of vaccination is encouraging, more data are needed to expand the existing understanding on this issue.

Funder

Emberi Eroforrások Minisztériuma

Nemzeti Kutatási Fejlesztési és Innovációs Hivatal

Publisher

SAGE Publications

Subject

Gastroenterology

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