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. 2021 May 4;356:577599. doi: 10.1016/j.jneuroim.2021.577599

Table 1.

Current and emerging COVID-19 vaccines and their relevance to MS.

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