| Frontiers in Immunology | |
| Serological Response to BNT162b2 Anti-SARS-CoV-2 Vaccination in Patients with Inflammatory Rheumatic Diseases: Results From the RHEUVAX Cohort | |
| Maria Vittoria Montemurro1  Antonio Giordano2  Maria Teresa Vietri3  Piero Ruscitti4  Maria Dora Pasquale5  Gelsomina Rozza5  Carlo Cannistrà5  Giuseppe Scalise5  Laura Bucci5  Silvia Scriffignano5  Antonio Ciancio5  Daniele Mauro5  Flavia Riccio5  Martina Patrone5  Claudio Di Vico5  Ilenia Pantano5  Luana Passariello6  Francesco Ciccia6  | |
| [1] Applied Clinical Sciences, University of L’Aquila, L’Aquila, Italy;Clinical Directorate, University Hospital of Università degli Studi della Campania “L. Vanvitelli”, Naples, Italy;Head Office, University Hospital of Università degli Studi della Campania “L. Vanvitelli”, Naples, Italy;;Rheumatology Unit, Department of Biotechnological &Rheumatology Unit, Department of Precision Medicine, Università degli Studi della Campania “L.Vanvitelli”, Naples, Italy;Unit of Clinical and Molecular Pathology, Department of Precision Medicine, Università degli Studi della Campania “L.Vanvitelli”, Naples, Italy; | |
| 关键词: COVID-19; vaccines; autoimmunity; rheumatic and muscoluskeletal disease; arthritis; connective tissue disease (CTD); | |
| DOI : 10.3389/fimmu.2022.901055 | |
| 来源: DOAJ | |
【 摘 要 】
ObjectiveIn the light of the current COVID-19 epidemic and the availability of effective vaccines, this study aims to identify factors associated with non-response to anti-SARS-CoV-2 vaccines as immunological alteration associated with immune rheumatic diseases (IRD) and immunosuppressive medications may impair the response to vaccination.MethodsVolunteers in the health profession community with IRD, age, and sex-matched controls (CTRL) who underwent vaccination with two doses of BNT162b2 were recruited for this study. Anti-Trimeric Spike protein antibodies were assayed eight ± one weeks after the second vaccine dose. Univariate and logistic regression analyses were performed to identify factors independently associated with non-response and low antibody titers.ResultsSamples were obtained from 237 IRD patients (m/f 73/164, mean age 57, CI 95% [56-59]): 4 autoinflammatory diseases (AI), 62 connective tissue diseases (CTD), 86 rheumatoid arthritis (RA), 71 spondylarthritis (SpA) and 14 vasculitis (Vsc). 232 CTRL were recruited (m/f 71/161, mean age 57, CI 95% [56-58]). Globally, IRD had a lower seroconversion rate (88.6% vs 99.6%, CI 95% OR [1.61-5.73], p<0.001) and lower antibody titer compared to controls (median (IQR) 403 (131.5-1012) versus 1160 (702.5-1675), p<0.001). After logistic regression, age, corticosteroid (CCS), Abatacept and Mycophenolate Mofetil (MMF) use were associated with non-response. Lower antibody titer was associated with the use of MMF, ABA, CCS, Rituximab, tumor necrosis factor inhibitor, JAK inhibitors, and higher age.ConclusionThe response to anti-SARS-CoV-2 vaccines is often impaired in IRD patients under treatment and may pose them at higher risk of severe COVID-19. Specific vaccination protocols are desirable for these patients.
【 授权许可】
Unknown