Table 2.
Clinical Scenarios of Patients with Systemic Autoimmune Disease at the Time of COVID-19 Vaccine Administration.
| Clinical scenarios | Clinical characteristics and treatments used | Opportunity to administer the COVID-19 vaccine |
|---|---|---|
| SAD in remission or with low level of activity with low dose of PDN and without ISSa | No evidence of clinical or immunological activity, no use of PDN or 7.5 mg/day doses | Ideal situation to receive the vaccine Level of antibody production against the vaccine (potentially) comparable to persons without SAD |
| SAD in remission or with low level of activity with low dose PDN and with ISSa | No evidence of clinical or immunological activity, no use of PDN or 7.5 mg/day doses and with ISS | Ideal situation to receive the vaccine Level of vaccine antibody production (potentially) lower than in people without SAD |
| SAD with moderate or severe activity level, with intermediate-high doses of PDN and with ISSa | Clinical evidence of serious activity or serious organ compromise (life-threatening) | Treat SAD, avoid organ damage and life risk Once remission induction is achieved, plan vaccination The use of ISS in high doses does not ensure the efficacy of the vaccine |
| SAD on RTX treatment (or anticipated to receive) | No clinical evidence of serious activity or serious organ compromise (not life-threatening) | With stable SAD, vaccinate and postpone RTX 4 weeks If vaccine is not available, defer RTX if condition allows If RTX already received, wait 4–8 weeks to vaccinate |
SAD: systemic autoimmune disease; PDN: prednisone; ISS: immunosuppressants; RTX rituximab.
Includes synthesis ISS, biologics, and Janus kinase inhibitors.