Coronavirus disease 2019 (COVID-19) vaccination is essential for patients with autoimmune inflammatory rheumatic diseases (AIIRD) to reduce the risk of morbidity and mortality associated with serious COVID-19 infection. With endemicity, waning of vaccine- and infection-acquired immunity, and development of SARS-CoV-2 variants, the need for additional doses of vaccines against serious illness in high-risk immunocompromised persons remains imperative. This review examines how immunomodulatory therapies affect vaccine-induced immune response in patients with AIIRD. Glucocorticoids, methotrexate, azathioprine, calcineurin inhibitors, mycophenolate mofetil, tumor necrosis factor inhibitors, and abatacept have been shown to variably attenuate both humoral and cellular immune responses to vaccination. Janus kinase inhibitors reduce humoral immune response. In contrast, sulfasalazine, leflunomide, belimumab, interleukin (IL)-17, IL-12/23, IL-6, and IL-1 inhibitors appear favorable, with mild or no impact on vaccine response. Although rituximab is known to profoundly diminish humoral immune response, cellular immunity is relatively preserved. Administering a third and subsequent vaccine dose or temporally coordinating the dosing of immunomodulatory drugs may improve vaccine effectiveness. Further research is needed to personalise vaccination strategies for AIIRD patients, considering their specific immunomodulatory treatments.
Keyphrases
- immune response
- coronavirus disease
- sars cov
- dendritic cells
- toll like receptor
- rheumatoid arthritis
- respiratory syndrome coronavirus
- oxidative stress
- end stage renal disease
- randomized controlled trial
- newly diagnosed
- systemic lupus erythematosus
- magnetic resonance imaging
- drug induced
- gene expression
- chronic kidney disease
- ejection fraction
- computed tomography
- high dose
- low dose
- extracorporeal membrane oxygenation
- inflammatory response
- acute respiratory distress syndrome
- respiratory failure
- rheumatoid arthritis patients