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Methotrexate and glucocorticoids, but not anticytokine therapy, impair the immunogenicity of a single dose of the BNT162b2 mRNA COVID-19 vaccine in patients with chronic inflammatory arthritis
- Source :
- Annals of the Rheumatic Diseases. 80:1635-1638
- Publication Year :
- 2021
- Publisher :
- BMJ, 2021.
-
Abstract
- Strategies aimed at expediting immunisation campaigns against COVID-19 include providing single vaccine doses to individuals with previous exposure to SARS-CoV-2 and delaying second doses. While such approaches are effective at the population level, immunogenicity yielded by one dose of vaccines in immunocompromised patients may be alarmingly low.1 2 Biological (b) and targeted synthetic (ts) disease-modifying antirheumatic drugs (DMARDs) interfere with the immune system at multiple levels and may variably reduce response to viral vaccines.3 Limited data on small numbers of rheumatic patients with variable diagnoses and treatments hamper definitive conclusions on the possible impact of immune-mediated inflammatory diseases, immunomodulatory drugs or both on the efficacy of the new generation of mRNA vaccines.4 5 Here we present interim data analysis on the immunogenicity of the BNT162b2 COVID-19 vaccine in 140 patients with chronic inflammatory arthritis all treated with b/tsDMARDs at the Division of Rheumatology of the IRCCS Policlinico San Matteo University Hospital of Pavia, receiving the first dose of vaccine between 24 and 31 March 2021. Patients were advised to discontinue both the b/tsDMARD and concomitant methotrexate around vaccination. In particular, the following suggestions were made: (1) for all the bDMARDs and methotrexate, withholding of therapy in the 7 days before and after vaccination; and (2) for tsDMARDs, withholding of therapy from the day before until day 7 after vaccination. For glucocorticoids and conventional synthetic DMARDs other than methotrexate, no modifications were advised. Blood samples were obtained immediately before vaccination and at day 21 after the first dose. Serum samples were tested using chemiluminescent immunoassay (LIAISON SARS-CoV-2 S1/S2 IgG; DiaSorin) for the quantitative characterisation of SARS-CoV-2 anti-S1 and anti-S2 IgG antibodies, with values >15 AU/mL indicating a positive result. Demographic and clinical variables were retrieved from the last available rheumatological assessment (median (IQR) 14 (5–19) days before vaccination) …
- Subjects :
- Male
0301 basic medicine
medicine.medical_specialty
COVID-19 Vaccines
Inflammatory arthritis
Immunology
General Biochemistry, Genetics and Molecular Biology
Arthritis, Rheumatoid
03 medical and health sciences
Immunogenicity, Vaccine
0302 clinical medicine
Immune system
Rheumatology
Internal medicine
medicine
Humans
Immunology and Allergy
Glucocorticoids
BNT162 Vaccine
030203 arthritis & rheumatology
biology
SARS-CoV-2
business.industry
Immunogenicity
COVID-19
Middle Aged
medicine.disease
Vaccination
Methotrexate
030104 developmental biology
Antirheumatic Agents
Concomitant
biology.protein
Female
Antibody
business
medicine.drug
Subjects
Details
- ISSN :
- 14682060 and 00034967
- Volume :
- 80
- Database :
- OpenAIRE
- Journal :
- Annals of the Rheumatic Diseases
- Accession number :
- edsair.doi.dedup.....1d0121f5cbf3e81c69220a67b053d752
- Full Text :
- https://doi.org/10.1136/annrheumdis-2021-220862