Shingrix Vaccination in Elderly Patients with Myasthenia Gravis
Elderly patients with myasthenia gravis can and should receive the Shingrix vaccine, as it is a non-live recombinant vaccine that is safe for immunocompromised individuals, including those on immunosuppressive therapy commonly used to treat MG. 1, 2
Primary Recommendation
The Centers for Disease Control and Prevention explicitly recommends Shingrix for immunocompromised adults aged ≥18 years, which includes patients with autoimmune conditions like myasthenia gravis who are on immunosuppressive therapy. 3, 2
Shingrix is the only appropriate zoster vaccine for patients with MG, as the live-attenuated vaccine (Zostavax) is absolutely contraindicated in immunocompromised patients due to risk of disseminated VZV infection. 2
For elderly patients (≥50 years), Shingrix is universally recommended regardless of underlying conditions, with demonstrated efficacy of 97.2% in adults aged 50+ years and 89.8% in adults aged 70+ years. 1, 3
Vaccination Schedule for MG Patients
Administer the 2-dose series with doses given 1-2 months apart for immunocompromised adults, which is a shortened schedule compared to the standard 2-6 month interval for immunocompetent individuals. 3, 2
The minimum interval between doses is 4 weeks if earlier administration is needed. 1
Safety Profile in Autoimmune Conditions
Shingrix can be safely administered to patients on immunosuppressive therapy, including glucocorticoids, biologics, JAK inhibitors, and rituximab. 2
Concomitant low-dose glucocorticoids (prednisone equivalent <10 mg/day) do not adversely impact vaccine response. 1, 2
Studies of patients with autoimmune conditions taking glucocorticoids showed only mild disease flares (4-17%) after Shingrix vaccination, with no serious adverse events. 1
Large database studies found no statistically significant increase in autoimmune disease flares following either dose of recombinant vaccine. 1
Evidence from MG-Specific Vaccine Studies
While the provided evidence focuses on COVID-19 vaccines rather than Shingrix specifically in MG patients, the safety data are reassuring:
COVID-19 mRNA vaccination in 91 patients with well-controlled MG showed no myasthenic crises and only 2 patients developed mild deterioration compared to baseline, with no clinical exacerbation regardless of age, immunosuppressant use, or history of myasthenic crisis. 4
This demonstrates that vaccines can be safely administered to stable MG patients, even those on immunosuppressants. 4
Important Clinical Considerations
The only absolute contraindication to Shingrix is a history of severe allergic reaction (anaphylaxis) to any vaccine component or after a previous dose—myasthenia gravis itself is not a contraindication. 2
Patients over 65 years develop fewer adverse effects from vaccination. 4
Common side effects include injection-site pain (most frequent), fatigue, myalgia, chills, fever, and headache, which are transient and resolve within days. 1, 4
Grade 3 injection site reactions occur in 9.5% of vaccine recipients compared to 0.4% with placebo. 1
Timing Considerations
Vaccination can proceed regardless of current MG disease activity, as long as the patient is clinically stable. 4
If the patient is starting or adjusting immunosuppressive therapy, ideally complete the 2-dose series before initiating treatment to maximize immune response, though vaccination can proceed even after immunosuppression has begun. 2
Consider administering between chemotherapy cycles (>7 days after last treatment) when feasible for patients on intensive immunosuppression, though this is not mandatory. 2
Critical Pitfall to Avoid
Never use live-attenuated Zostavax in patients with myasthenia gravis—only Shingrix (recombinant zoster vaccine) is appropriate for this population. 3, 2
Prior receipt of Zostavax does not preclude Shingrix vaccination; patients should receive the full 2-dose Shingrix series at least 2 months after any previous Zostavax dose. 1, 2
Clinical Rationale
Elderly patients with MG face elevated baseline risk for herpes zoster due to both advanced age and immunosuppressive therapy. 1, 2
The recombinant vaccine contains only a viral glycoprotein fragment with an adjuvant, not live virus, eliminating any theoretical risk of vaccine-strain infection. 2
Real-world effectiveness demonstrates 70.1% vaccine effectiveness for 2 doses and 56.9% for 1 dose, emphasizing the importance of completing the full series. 2
Protection persists for at least 8 years with minimal waning, maintaining efficacy above 83.3% during this period. 1, 2