Vaccination and immunotherapies in neuroimmunological diseases
- PMID: 35388213
- PMCID: PMC8985568
- DOI: 10.1038/s41582-022-00646-5
Vaccination and immunotherapies in neuroimmunological diseases
Abstract
Neuroimmunological diseases and their treatment compromise the immune system, thereby increasing the risk of infections and serious illness. Consequently, vaccinations to protect against infections are an important part of the clinical management of these diseases. However, the wide variety of immunotherapies that are currently used to treat neuroimmunological disease - particularly multiple sclerosis and neuromyelitis optica spectrum disorders - can also impair immunological responses to vaccinations. In this Review, we discuss what is known about the effects of various immunotherapies on immunological responses to vaccines and what these effects mean for the safe and effective use of vaccines in patients with a neuroimmunological disease. The success of vaccination in patients receiving immunotherapy largely depends on the specific mode of action of the immunotherapy. To minimize the risk of infection when using immunotherapy, assessment of immune status and exclusion of underlying chronic infections before initiation of therapy are essential. Selection of the required vaccinations and leaving appropriate time intervals between vaccination and administration of immunotherapy can help to safeguard patients. We also discuss the rapidly evolving knowledge of how immunotherapies affect responses to SARS-CoV-2 vaccines and how these effects should influence the management of patients on these therapies during the COVID-19 pandemic.
© 2022. Springer Nature Limited.
Conflict of interest statement
A.W. reports personal fees from Alexion, Biogen, Celgene, Merck, Novartis, Sanofi, Roche and Teva that are not directly related to the manuscript. M.L. reports institutional funding from Sanofi Pasteur and personal fees from AbbVie, Bayer, Bristol Myers Squibb, Merck Healthcare and Pfizer that are not directly related to the manuscript. M.B. reports institutional funding from Alexion, Biogen, BMS, Merck, Novartis, and Roche and personal fees from Biogen and Novartis that are not directly related to the manuscript. H.-P.H. reports personal fees from Bayer Healthcare, Biogen, Celgene BMS, GeNeuro, Merck, Novartis, Roche, TG Therapeutics and VielaBio that are not directly related to the manuscript. U.K.Z. reports personal fees from Alexion, Almirall, Bayer, Biogen, Janssen, Merck Serono, Novartis, Octapharm, Roche, Sanofi Genzyme, and Teva as well as grants from the European Union, German Federal Ministry of Education and Research, German Federal Ministry for Economic Affairs and Climate Action, and Deutsche Forschungsgemeinschaft that are not directly related to the manuscript.
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