Table 1.
COVID-19 vaccine | mRNA vaccines (Moderna, Pfizer) | Inactivated (Sinopharm), protein-based (Novavax), and DNA (Inovio) vaccines | Human viral vector vaccine (Johnson & Johnson) | Simian viral vector vaccine (AstraZeneca) | Live-attenuated vaccine (Meissa) |
---|---|---|---|---|---|
Number of doses | Two | Two | One | Two | One |
Severe immune-mediated adverse events | Rare facial palsy | None reported | One report of MS relapse in an untreated patient | One report of vaccine-related TM and one report of MS relapse in an untreated patient | Unknown, but has a higher potential for immune-mediated adverse events and a higher risk of causing COVID-19 infection in immunocompromised patients |
IFN-B, GA, teriflunomide, and natalizumab | No major safety or efficacy concerns | No major safety or efficacy concerns | No major safety or efficacy concerns | No major safety or efficacy concerns | Not preferred |
Fumarates | Possible decreased vaccine efficacy in patients with severe lymphopenia Consider dose interruption in severely lymphopenic patients to allow for lymphocytic recovery prior to vaccination |
Possible decreased vaccine efficacy in patients with severe lymphopenia Consider dose interruption in severely lymphopenic patients to allow for lymphocytic recovery prior to vaccination |
Possible decreased vaccine efficacy in patients with severe lymphopenia Consider dose interruption in severely lymphopenic patients to allow for lymphocytic recovery prior to vaccination |
Possible decreased vaccine efficacy in patients with severe lymphopenia Consider dose interruption in severely lymphopenic patients to allow for lymphocytic recovery prior to vaccination |
Not preferred and may be especially dangerous in patients with severe lymphopenia |
S1P modulators | Possible decreased cellular vaccine response Interruption of treatment not recommended to avoid MS rebound |
Possible decreased cellular vaccine response Interruption of treatment not recommended to avoid MS rebound |
Possible decreased cellular vaccine response Interruption of treatment not recommended to avoid MS rebound |
Possible decreased cellular vaccine response Interruption of treatment not recommended to avoid MS rebound |
Contraindicated |
Ocrelizumab | Possible decreased humoral > cellular vaccine response Consider vaccination between month 3 and 5 of the treatment cycle to maximize vaccine efficacy Consider delaying infusion to one month after 2nd vaccine |
Possible decreased humoral > cellular vaccine response Consider vaccination between month 3 and 5 of the treatment cycle to maximize vaccine efficacy Consider delaying infusion to one month after 2nd vaccine |
Possible decreased humoral > cellular vaccine response Consider vaccination between month 3 and 5 of the treatment cycle to maximize vaccine efficacy Consider delaying infusion to one month after vaccination |
Possible decreased humoral > cellular vaccine response Consider vaccination between month 3 and 5 of the treatment cycle to maximize vaccine efficacy Consider delaying infusion to one month after 2nd vaccine |
Contraindicated |
Ofatumumab | Possible decreased humoral > cellular vaccine response Consider vaccination one month after injection and delay next injection for one month after 2nd vaccine |
Possible decreased humoral > cellular vaccine response Consider vaccination one month after injection and delay next injection for one month after 2nd vaccine |
Possible decreased humoral > cellular vaccine response Consider vaccination one month after injection and delay next injection for one month after vaccination |
Possible decreased humoral > cellular vaccine response Consider vaccination one month after injection and delay next injection for one month after 2nd vaccine |
Contraindicated |
Rituximab | Possible decreased humoral > cellular vaccine response Consider vaccination 3 to 6 months after injection and delay next injection for 4–6 weeks after 2nd vaccine |
Possible decreased humoral > cellular vaccine response Consider vaccination 3 to 6 months after injection and delay next injection for 4–6 weeks after 2nd vaccine |
Possible decreased humoral > cellular vaccine response Consider vaccination 3 to 6 months after injection and delay next injection for 4–6 weeks after vaccination |
Possible decreased humoral > cellular vaccine response Consider vaccination 3 to 6 months after injection and delay next injection for 4–6 weeks after 2nd vaccine |
Contraindicated |
Alemtuzumab | Possible decreased cellular > humoral vaccine response Consider vaccination six months after completion of treatment course Consider delaying treatment course to one month after 2nd vaccine |
Possible decreased cellular > humoral vaccine response Consider vaccination six months after completion of treatment course Consider delaying treatment course to one month after 2nd vaccine |
Possible decreased cellular > humoral vaccine response Consider vaccination six months after completion of treatment course Consider delaying treatment course to one month after vaccination |
Possible decreased cellular > humoral vaccine response Consider vaccination six months after completion of treatment course Consider delaying treatment course to one month after 2nd vaccine |
Contraindicated |
Cladribine | Possible decreased humoral > cellular vaccine response Consider vaccination six months after completion of the second treatment cycle Consider delaying treatment course to one month after 2nd vaccine |
Possible decreased humoral > cellular vaccine response Consider vaccination six months after completion of the second treatment cycle Consider delaying treatment course to one month after 2nd vaccine |
Possible decreased humoral > cellular vaccine response Consider vaccination six months after completion of the second treatment cycle Consider delaying treatment course to one month after vaccination |
Possible decreased humoral > cellular vaccine response Consider vaccination six months after completion of the second treatment cycle Consider delaying treatment course to one month after 2nd vaccine |
Contraindicated |
Other considerations | Widely available vaccines and many MS patients received them without red flags | Inactivated and protein-based vaccines have a long track record of safety and compatibility with MS DMTs | Single dosing is convenient for patients on cell-depleting DMTs who wish to coordinate vaccine timing with DMT dosing to maximize vaccine efficacy | More reports of demyelinating side effects than other COVID-19 vaccines but they remain rare, isolated events | Lower risk for COVID-19 infection in untreated MS patients but possibly higher risk for inducing relapse |