Skip to main content
. 2022 Sep 30;74(6):1208–1222. doi: 10.1007/s43440-022-00424-6

Table 3.

Potential impact of MS therapies on COVID-19 clinical course and stratification risk of MS treatment (adapted and modified from: Bhise and Dhib-Jalbut [98])

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