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Cellular and humoral vaccination response under immunotherapies — German consensus on vaccination strategies in neurological autoimmune diseases

  • Background: With the development of highly effective disease-modifying treatments, vaccinations are becoming increasingly important in people with neurological autoimmune diseases. However, questions regarding the safety and efficacy of vaccinations under immunotherapy remain. Objective: To provide recommendations on types and timing of vaccinations for people with neuroimmunological diseases under different immunotherapies. Design: Our study presents a German evidence-based expert consensus on vaccination under immunotherapies in neurological autoimmune diseases. Methods: Based on literature research, a consortium of experts evaluated the quality of evidence, integrated clinical experience, and responded to a questionnaire determining an agreement (>75%) on statements concerning vaccination upon immune therapies in neuroimmunological diseases. Results: The specific humoral and cellular response to vaccination can be compromised under alemtuzumab, azathioprine, cladribine,Background: With the development of highly effective disease-modifying treatments, vaccinations are becoming increasingly important in people with neurological autoimmune diseases. However, questions regarding the safety and efficacy of vaccinations under immunotherapy remain. Objective: To provide recommendations on types and timing of vaccinations for people with neuroimmunological diseases under different immunotherapies. Design: Our study presents a German evidence-based expert consensus on vaccination under immunotherapies in neurological autoimmune diseases. Methods: Based on literature research, a consortium of experts evaluated the quality of evidence, integrated clinical experience, and responded to a questionnaire determining an agreement (>75%) on statements concerning vaccination upon immune therapies in neuroimmunological diseases. Results: The specific humoral and cellular response to vaccination can be compromised under alemtuzumab, azathioprine, cladribine, cyclophosphamide, CD19/CD20 antibodies (inebilizumab, ocrelizumab, ofatumumab, rituximab, ublituximab), dimethyl fumarate/diroximel fumarate, FcRn inhibitors (efgartigimod, rozanolixizumab), complement C5 inhibitors (eculizumab, ravulizumab, zilucoplan), interleukin-6 receptor antibodies (tocilizumab, satralizumab), intravenous immunoglobulins, long-term steroid administration, methotrexate, mitoxantrone, mycophenolate mofetil, tacrolimus, teriflunomide, tumor necrosis factor-α blockers, and sphingosine-1-phosphate receptor modulators (fingolimod, ozanimod, ponesimod, siponimod), as well as after autologous stem cell transplantation. The lymphocyte count can have an influence here. Overall, it is generally advisable to complete vaccination before starting immunotherapy. However, in the case of an active inflammatory disease course with possible irreversible neurological deficits, a delay in therapy initiation until immunization has been completed cannot be justified. The application of live vaccines is contraindicated for most therapies and is only recommended after a strict risk–benefit assessment. Conclusion: Vaccinations are necessary for individuals on immunotherapy to reduce the risk of infections and the associated risk of worsening neurological autoimmune diseases. However, the humoral and cellular vaccination response may be impaired under immunotherapy necessitating close monitoring. Here, we provide applicable recommendations to optimize immunization for individuals receiving immunotherapy due to a neurological autoimmune disease.show moreshow less

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Metadaten
Author:Muriel Schraad, Mathias Mäurer, Anke SalmenORCiD, Tobias Ruck, Timo UphausORCiD, Vinzenz FleischerORCiD, Felix LuessiORCiD, Maria ProtopapaORCiD, Falk Steffen, Nicholas Hanuscheck, Katrin PapeORCiD, Tobias BrummerORCiD, Josef Shin, Thomas Korn, Luisa KlotzORCiD, Jan D. LünemannORCiD, Marc PawlitzkiORCiD, Martin S. Weber, Antonios BayasORCiDGND, Brigitte Wildemann, Hans-Peter HartungORCiD, Florian Then Bergh, Clemens Warnke, Uwe K. Zettl, Achim Berthele, Aiden Haghikia, Ralf LinkerORCiD, Hayrettin TumaniORCiD, Sven G. Meuth, Bernhard HemmerORCiD, Heinz Wiendl, Tania KümpfelORCiD, Ralf Gold, Stefan BittnerORCiD, Frauke ZippORCiD
URN:urn:nbn:de:bvb:384-opus4-1271572
Frontdoor URLhttps://opus.bibliothek.uni-augsburg.de/opus4/127157
ISSN:1756-2864OPAC
Parent Title (English):Therapeutic Advances in Neurological Disorders
Publisher:SAGE Publications
Place of publication:London
Type:Article
Language:English
Date of first Publication:2025/12/12
Publishing Institution:Universität Augsburg
Release Date:2025/12/22
Tag:immunotherapies; neuroimmunological diseases; neurological autoimmune diseases; vaccination
Volume:18
First Page:1
Last Page:40
DOI:https://doi.org/10.1177/17562864251396006
Institutes:Medizinische Fakultät
Medizinische Fakultät / Universitätsklinikum
Medizinische Fakultät / Lehrstuhl für Neurologie
Dewey Decimal Classification:6 Technik, Medizin, angewandte Wissenschaften / 61 Medizin und Gesundheit / 610 Medizin und Gesundheit
Licence (German):CC-BY-NC 4.0: Creative Commons: Namensnennung - Nicht kommerziell