Full Papers
Comparison of SARS-COV-2 humoral response between rheumatoid arthritis, psoriatic arthritis and spondyloarthritis patients and controls in two unvaccinated cohorts
A. Ruyssen-Witrand1, C. Dimeglio2, E. Nogue3, N. Molinary4, T. Pham5, C. Gaujoux-Viala6, C. Miceli-Richard7, O. Fogel8, F. Herin9, G. Martin-Blondel10, F. Berenbaum11, V. Breuil12, I. Chary-Valckenaere13, C. Confavreux14, V. Devauchelle-Pensec15, B. Fautrel16, R.-M. Flipo17, D. Mulleman18, C. Richez19, A. Tournadre20, O. Vittecoq21, A. Constantin22, J. Izopet23, J. Morel24
- Department of Rheumatology, Toulouse University Hospital, Centre d’Investigation Clinique de Toulouse CIC1436, Inserm, Paul Sabatier University, Toulouse, France. ruyssen-witrand.a@chu-toulouse.fr
- CHU Toulouse, Hôpital Purpan, Virology Laboratory, Toulouse; INSERM UMR1291 - CNRS UMR5051, Toulouse Institute for Infectious and Inflammatory Diseases (INFINITy), Toulouse, France.
- Clinical Research and Epidemiology Unit, CHU Montpellier, University of Montpellier, France.
- UA11 Institute of Epidemiology and Public Health, INSERM, University of Montpellier, France.
- Department of Rheumatology, Centre Hospitalier Universitaire Sainte Marguerite, Université Aix Marseille, France.
- Desbrest Institute of Epidemiology and Public Health (IDESP), Université de Montpellier, INSERM, Department of Rheumatology, CHU Nîmes, Montpellier, France.
- Service de Rhumatologie, Université de Paris, Hôpital Cochin Port Royal, AP-HP, and Unité Mixte AP-HP/Institut Pasteur, Institut Pasteur, Immunoregulation Unit, Paris, France.
- Department of Rheumatology, Cochin University Hospital, Assistance Publique-Hôpitaux de Paris, France.
- Occupational Diseases Department, Toulouse University Hospital; Inserm UMR 1295: Center for Research in Population Health (CERPOP), Department of Epidemiology and Public Health, University of Toulouse, France.
- Service des Maladies Infectieuses et Tropicales, CHU de Toulouse & Institut Toulousain des Maladies Infectieuses et Inflammatoires (Infinity), INSERM UMR1291 - CNRS UMR5051, Université Toulouse, France.
- Sorbonne University, CRSA, INSERM Department of Rheumatology, AP-HP Saint-Antoine Hospital, Paris, France.
- Université Côte d’Azur (UCA), Service de Rhumatologie, CHU de Nice, Hôpital Pasteur, Nice; UMR E-4320 MATOs CEA/iBEB/SBTN, Faculté de Médecine, Université Nice Sophia Antipolis, Nice, France.
- Department of Rheumatology, Nancy University Hospital Nancy, and IMoPA 7561 CNRS, University of Lorraine, Vandoeuvre‑Lès‑Nancy, Nancy, France.
- University of Lyon, INSERM U1033 LYOS and Department of Rheumatology, Groupement Hospitalier Sud, Hospice Civils de Lyon, Pierre-Bénite, France.
- Department of Rheumatology, CHU de Brest, and INSERM 1227 LBAI Université de Bretagne Occidentale, Centre de Référence des Maladies Auto-Immunes Rares de l'Adulte, Brest, France.
- Sorbonne Université, Assistance Publique Hôpitaux de Paris, Service de Rhumatologie, Groupe Hospitalier Pitié-Salpêtrière, Institut Pierre Louis d’Épidémiologie et de Santé Publique Département de Biostatistiques, INSERM UMR 1136, Paris, France.
- Department of Rheumatology, Hôpital Roger Salengro, University of Lille, France.
- Department of Rheumatology, Regional University Hospital Centre Tours, France.
- Bordeaux University Hospital, Department of Rheumatology, Reference Center for Rare Systemic Autoimmune and Autoinflammatory Diseases RESO, and Bordeaux University, CNRS, Immuno ConcEpT, UMR 5164, Bordeaux, France.
- Department of Rheumatology, CHU Clermont-Ferrand, France.
- Rouen University, Rouen University Hospital, Service de Rhumatologie, CIC-CRB 1404, INSERM, U1234, Rouen, France.
- Department of Rheumatology, Toulouse University Hospital INSERM UMR1291 - CNRS UMR5051, Toulouse Institute for Infectious and Inflammatory Diseases (INFINITy) and University Toulouse, France.
- CHU Toulouse, Hôpital Purpan, Virology Laboratory, Toulouse; INSERM UMR1291 - CNRS UMR5051, Toulouse Institute for Infectious and Inflammatory Diseases (INFINITy), Toulouse, France.
- Department of Rheumatology, CHU and University of Montpellier, Phymedexp, Université de Montpellier, INSERM, CNRS, Montpellier, France.
CER17420
2024 Vol.42, N°11
PI 2141, PF 2149
Full Papers
Free to view
(click on article PDF icon to read the article)
PMID: 39436731 [PubMed]
Received: 27/12/2023
Accepted : 18/03/2024
In Press: 17/10/2024
Published: 04/11/2024
Abstract
OBJECTIVES:
To compare the humoral response after a SARS-CoV-2 infection in an inflammatory rheumatic disease population with a healthy control population in a case-control study.
METHODS:
Cases: between March and September 2021, all consecutive unvaccinated patients followed for rheumatoid arthritis (RA), spondyloarthritis (SpA) or psoriatic arthritis (PsA) in 16 hospitals in France were systematically screened with a SARS-CoV-2 serological test. Patients with a positive test were included in the COVID-RIC-2 cohort. Controls: between June and July 2020, healthcare professionals working in the Toulouse University Hospital were screened with a SARS-CoV-2 serological test. Those with a positive test were included in the COVID-BIOTOUL cohort and matched to those from COVID-RIC-2 by age, sex and time-sampling on infection date. Analyses: total SARS-CoV-2 antibody titres were centrally measured and compared.
RESULTS:
95 patients from COVID-RIC-2 (mean age 49 years, 76% females, median delay of COVID infection: 149 days) including 48 RA, 33 SpA and 14 PsA were compared to 95 matched controls. Globally, there was no significant difference of SARS-CoV-2 antibody titres between both populations: 155 Binding Antibody Units (BAU) (IQR:7-376) in COVID-RIC-2 vs. 120 BAU (IQR:35-320) in COVID-BIOTOUL. There was a trend towards higher antibody titres in patients from COVID-RIC-2 with severe COVID-19 symptoms. In COVID-RIC-2, there was no impact of age, sex, time-sampling or underlying disease on antibody titres and patients taking glucocorticoids, abatacept or rituximab trended toward having lower antibody titres after COVID-19 infection.
CONCLUSIONS:
This study provides reassuring data on humoral response after COVID-19 infection in patients treated with disease-modifying anti-rheumatic drugs.