Table 3.
Medication | Potential benefit in COVID-19 | Potential adverse effect in COVID-19 | Risk of MS treatment | Currently receiving | New start |
---|---|---|---|---|---|
Interferon β | Reduced viral replication; inhibition of proinflammatory cytokines | Unknown | Lowest | Continue | Yes* |
Glatiramer acetate | Counteract proinflammatory responses | Unknown | Lowest | Continue | Yes |
Dimethyl fumarate | Reduced innate immune response to virus | Lymphopenia-related increased risk of infection and impaired viral clearance | Low | Continue | Yes |
Teriflunomide | Anti-viral effect | Lymphopenia-related increased risk of infection and impaired viral clearance | Low | Continue | Yes |
Fignolimod/siponimod/ozanimod | Lymphopenia may be beneficial for pneumonia and ARDS | Lymphopenia resulting in reduced viral clearance | Medium | Continue | Yes |
Natalizumab | May interfere with SARS-CoV-2 host cell entry | Reduced SARS-CoV-2 clearance from the CNS and gut | Medium | Extend to 6-week intervals | Yes |
Rituximab/okrelizumab/ofatumumab | Unknown | Increased risk of infection and impaired viral clearance | Medium–high | Extend interval based on B-cell counts | Yes |
Cladribine | Unknown | Lymphopenia-related increased risk of infection and impaired viral clearance | High | Delay/switch | No** |
Alemtuzumab | Unknown | Lymphopenia-related increased risk of infection and impaired viral clearance | High | Delay/switch | No |
Hematopoietic stem cell therapy | Unknown | Unknown | High | Delay/switch | No |
ARDS acute respiratory distress syndrome, CNS central nervous system
*Yes: treatment can be initiated
**No: postpone treatment